clinical research scientist salary

Salary.com Articles

• Should Some Employees Be Allowed to Start Work Late?
• Do Work-at-Home Jobs Pay Less Than Office Jobs?
• How to Get Your Way in Business and Life
• 7 High-Growth Jobs That Don't Require a College Degree
• 6 Reasons You Can't Stay Productive

Advertise with Us | Partnerships | About Salary.com | Salary Wizard™ is a registered trademark | ©2024 Salary.com. All rights reserved.

Resume Builder

• Resume Experts
• Search Jobs
• Search for Talent
• Employer Branding
• Outplacement

Clinical Scientist Salary in The United States

The average Clinical Scientist Salary in The United States is $91,300 per year . Salaries range from $65,000 to $114,500 . The average Clinical Scientist Hourly Wage is $51.00 per hour . Hourly wages range from $25.00 to $67.34 . Salaries and wages depend on multiple factors including geographic location, experience, seniority, industry, education etc.

What is the Average Annual Salary of Clinical Scientist in The United States ?

What is the Average Hourly Wage of Clinical Scientist in The United States ?

Where do Clinical Scientists earn more in The United States ?

Other salaries.

Create a Resume and Cover Letter in Minutes with Professional Templates

Create a Resume in Minutes with Professional Resume Templates

Explore Jobs

• Jobs Near Me
• Remote Jobs
• Full Time Jobs
• Part Time Jobs
• Entry Level Jobs
• Work From Home Jobs

Find Specific Jobs

• $15 Per Hour Jobs
• $20 Per Hour Jobs
• Hiring Immediately Jobs
• High School Jobs
• H1b Visa Jobs

Explore Careers

• Business And Financial
• Architecture And Engineering
• Computer And Mathematical

Explore Professions

• What They Do
• Certifications
• Demographics

Best Companies

• Health Care
• Fortune 500

Explore Companies

• CEO And Executies
• Resume Builder
• Career Advice
• Explore Majors
• Questions And Answers
• Interview Questions

What is a clinical research scientist and how to become one

A clinical research scientist is a professional who conducts laboratory research and examinations to identify diseases and establish treatment plans. They work in various organizations, such as pharmaceutical companies, hospitals, and universities, and are responsible for documenting processes and recording results. Clinical research scientists use specialized equipment to study bacteria and diseases and may interact with patients during test treatments. They must have excellent communication skills and extensive knowledge of the medical industry. In addition, they are responsible for ensuring compliance with company and FDA requirements, interacting with marketing companies and external investigators, and managing medical writing vendors. They may also lead and prepare clinical trial amendments, develop study protocols, and provide clinical expertise to monitors, physicians, and sites.

How long does it takes to become a clinical research scientist?

It typically takes 5-6 years to become a clinical research scientist:

• Years 1-4: Obtaining a Bachelor's degree in a relevant field such as biology, chemistry, or a related scientific discipline.
• Years 5-6: Accumulating the necessary work experience, starting with 3-6 months of on-site training, followed by 6-12 months of on-the-job training while working on clinical research projects.

Avg. Salary $99,160

Avg. Salary $59,228

Growth Rate 6 %

Growth Rate 0.3 %

American Indian and Alaska Native 0.51 %

Asian 13.45 %

Black or African American 2.47 %

Hispanic or Latino 13.95 %

Unknown 7.43 %

White 62.19 %

female 64.60 %

male 35.40 %

American Indian and Alaska Native 3.00 %

Asian 7.00 %

Black or African American 14.00 %

Hispanic or Latino 19.00 %

White 57.00 %

female 47.00 %

male 53.00 %

Stress level is manageable

Complexity Level is advanced

7 - challenging

Work Life balance is fair

Clinical Research Scientist career paths

Clinical research scientists often move into management roles, such as clinical trial managers, clinical study managers, or clinical project managers. They may also become directors of clinical operations. Some may choose to stay in research, becoming senior clinical research scientists or scientists. Others might take on roles like quality assurance managers, regulatory affairs managers, or business managers.

Key steps to become a clinical research scientist

Explore clinical research scientist education requirements.

The educational requirements for a clinical research scientist typically include a bachelor's degree in biology, nursing, biochemistry, pharmacy, or chemistry. According to Professor, Pharmacology & Toxicology; Professor, Obstetrics & Gynecology, David Cool Ph.D. from Wright State University, "Universities are starting to create new degree programs designed to train people to run clinical trials." Additionally, obtaining certification as a Clinical Research Professional or Medical Laboratory Technician can further enhance job prospects.

Most common clinical research scientist degrees

Bachelor's

Master's

Start to develop specific clinical research scientist skills

Clinical research scientists handle various tasks. They ensure compliance with FDA requirements, interact with marketing companies, and facilitate IRB approval. They also manage medical writing vendors, perform routine laboratory maintenance, and develop protocols for clinical studies. As Badri Roysam D.Sc., Hugh Roy and Lillie Cranz Cullen University Professor and Chair, Electrical & Computer Engineering Department at the University of Houston, says, "The fundamentals of the discipline, and critical thinking skills will continue to be important."

Complete relevant clinical research scientist training and internships

Research clinical research scientist duties and responsibilities.

A clinical research scientist's responsibilities include ensuring compliance with FDA regulations, interacting with investigators and clinical operations teams, and managing day-to-day interactions with study sites. They also facilitate IRB approval, compile clinical study reports, and mentor and train other clinical research associates. As Professor of Biomedical Sciences Lisa Cuchara Ph.D. from Quinnipiac University puts it, "The first and foremost would be Critical Thinking. I can ask anyone on the street what xyz is and they can look it up, but can they provide advice or interpret."

• Supervise and manage planning, implementation, conduct and reporting of assign early phase international clinical studies in oncology.
• Facilitate IRB approval, when require.
• Compile and submit reports to U.S. FDA.
• Provide draft responses to FDA questions to senior management.

Prepare your clinical research scientist resume

When your background is strong enough, you can start writing your clinical research scientist resume.

You can use Zippia's AI resume builder to make the resume writing process easier while also making sure that you include key information that hiring managers expect to see on a clinical research scientist resume. You'll find resume tips and examples of skills, responsibilities, and summaries, all provided by Zippi, your career sidekick.

Choose From 10+ Customizable Clinical Research Scientist Resume templates

Apply for clinical research scientist jobs

Now it's time to start searching for a clinical research scientist job. Consider the tips below for a successful job search:

• Browse job boards for relevant postings
• Consult your professional network
• Reach out to companies you're interested in working for directly
• Watch out for job scams

How Did You Land Your First Clinical Research Scientist Job

Are you a Clinical Research Scientist?

Share your story for a free salary report.

Average clinical research scientist salary

The average Clinical Research Scientist salary in the United States is $99,160 per year or $48 per hour. Clinical research scientist salaries range between $63,000 and $154,000 per year.

What Am I Worth?

How do clinical research scientists rate their job?

Updated June 25, 2024

Editorial Staff

The Zippia Research Team has spent countless hours reviewing resumes, job postings, and government data to determine what goes into getting a job in each phase of life. Professional writers and data scientists comprise the Zippia Research Team.

Clinical Research Scientist Related Careers

• Clinical Associate
• Clinical Coordinator
• Clinical Project Manager
• Clinical Research Assistant
• Clinical Research Associate
• Clinical Research Coordinator
• Clinical Research Manager
• Clinical Trial Manager
• Coordinator And Research Assistant
• Research Administrator
• Research Coordinator
• Research Nurse
• Research Project Coordinator
• Research Scientist

Clinical Research Scientist Related Jobs

• Clinical Associate Jobs
• Clinical Coordinator Jobs
• Clinical Project Manager Jobs
• Clinical Research Assistant Jobs
• Clinical Research Associate Jobs
• Clinical Research Coordinator Jobs
• Clinical Research Manager Jobs
• Clinical Trial Manager Jobs
• Coordinator And Research Assistant Jobs
• Research Administrator Jobs
• Research Coordinator Jobs
• Research Nurse Jobs
• Research Project Coordinator Jobs
• Research Scientist Jobs
• Scientist Jobs

What Similar Roles Do

• What Does a Clinical Associate Do
• What Does a Clinical Coordinator Do
• What Does a Clinical Project Manager Do
• What Does a Clinical Research Assistant Do
• What Does a Clinical Research Associate Do
• What Does a Clinical Research Coordinator Do
• What Does a Clinical Research Manager Do
• What Does a Clinical Trial Manager Do
• What Does a Coordinator And Research Assistant Do
• What Does a Research Administrator Do
• What Does a Research Coordinator Do
• What Does a Research Nurse Do
• What Does a Research Project Coordinator Do
• What Does a Research Scientist Do
• What Does a Scientist Do

Resume For Related Jobs

• Clinical Associate Resume
• Clinical Coordinator Resume
• Clinical Research Assistant Resume
• Clinical Research Associate Resume
• Clinical Research Coordinator Resume
• Research Coordinator Resume
• Research Nurse Resume
• Research Project Coordinator Resume
• Research Scientist Resume
• Scientist Resume
• Senior Clinical Research Associate Resume
• Senior Research Associate Resume
• Study Coordinator Resume
• Zippia Careers
• Executive Management Industry
• Clinical Research Scientist

Browse executive management jobs

THSTI looking for Research Scientist, Clinical Research Associate - Salary upto Rs. 1,10,000 pm

BRIC-Translational Health Science and Technology Institute (THSTI) is an Institute of the Biotechnology Research and Innovation Council, Department of Biotechnology, Ministry of Science & Technology, Govt. of India. The institute is an integral part of the interdisciplinary NCR Biotech Science Cluster located at Faridabad, and is designed as a dynamic, interactive organization with the mission to conduct innovative translational research and to develop research collaborations across disciplines and professions to translate concepts into products to improve human health.

Post : Research Scientist, Clinical Research Associate

Research Scientist (Bioinformatics) Name of the Project : Clinical Development Services Agency - CDSA  Number of posts : One  Emoluments : Rs. 1,10,000/-  Duration : One Year  Age : 40 years Essential qualification and work experience : MD or MVSc or M.Tech with minimum 2 years’ relevant post qualification research experience OR PhD in Life Sciences / Computational Science / Bioinformatics / Genomics from a recognized University with minimum 6 months relevant post qualification research experience.  Desirable : Work experience in metagenomics and bacterial genomics. Job profile : Research and support to the ongoing big data analysis or next generation DNA sequencing data analysis or Proteomics and metabolomics data analysis

Clinical Research Associate Name of the Project : DBT Neo-Sepsis  Number of posts : One  Emoluments : Rs. 60,760/-  Duration Up to : 31st March 2025 (can be extended further)  Age : 35 Years  Minimum Educational Qualification and Experience : Bachelors in Life Sciences with minimum three years of relevant clinical trial monitoring experience. OR  • Master’s degree/ diploma, life sciences, pharmacy, public health, healthcare or other related discipline with minimum 2 years of relevant clinical trial monitoring experience.  • MBBS/ BDS/ BHMS/ BAMS/ BPT preferred Job profile The Study Monitor/ CRA conduct monitoring visits for assigned trial protocol and trial sites. Overall responsibilities are to ensure that the trial is being conducted in accordance with the protocol, standard operating procedures, good clinical practice, and applicable regulatory requirement. • Performs site monitoring throughout the trial which involves visiting the trial sites on a regular basis (site initiation to site closeout) in accordance with contracted scope of work.  • Performs quality functions and executing quality programs (clinical operations, clinical laboratory) as per GCP/GCLP and regulations  • Completes appropriate therapeutic, protocol and clinical research training to perform job duties.  • Setting up the trial sites such that each center has the trial materials, including the trial drug while ensuring all trial supplies are accounted for Administers protocol and related trial training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.  • May provide training and assistance to junior clinical staff.  • Creates and maintains appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required trial documentation.  • Manages the progress of assigned studies by tracking regulatory/ IEC submissions and approvals, recruitment and enrolment, CRF completion and submission, and data query generation and resolution.  • Verifying that data entered on to the CRFs is consistent with participant clinical notes (source data/ document verification)  • Writing visit reports and Filing and collating trial documentation and reports.  • Archiving trial documentation and correspondence.  • Evaluates the quality and integrity of trial site practices related to the proper conduct of the protocol and adherence to applicable regulations.  • Escalates quality issues to the Quality Manager, Project Manager and/ or senior management.  • Work with Clinical Portfolio Management on other projects as directed and other internal departments on their requirements as and when required.  Skills: -  • Computer skills including proficiency in use of Microsoft Office applications  • Basic knowledge and ability to apply GCP and applicable regulatory guidelines.  • Strong written and verbal communication skills including good command of English required.  • Excellent organizational and problem-solving skills.  • Effective time management skills and ability to manage competing priorities.

General Terms & Conditions a) (i) S. No. 1 The positions will be hired initially for a period of one year with a probation period of six months. The extension will be granted subject to satisfactory performance of the incumbents and tenure of the project for which they are selected. Those appointed to these positions will not have any claim for regularization of their employment  (ii) S. No. II This is short-term positions for a period of one year with a probation period of three months. The extension will be granted subject to satisfactory performance of the incumbents and tenure of the project for which they are selected. Those appointed to these positions will not have any claim for regularization of their employment.  b) All educational, professional and technical qualification should be from a recognized Board/University.  c) The experience requirement specified above shall be the experience acquired after obtaining the minimum educational qualifications specified for the post.  d) Closing date of online application will be the CRUCIAL DATE for determining eligibility with regard to age, essential qualification etc.  e) Number of positions to be hired, age limit, qualification, experience and other requirements may be relaxed at the discretion of the competent authority, in case of candidates who are otherwise suitable. In case candidates are not found suitable for the posts notified, they can be offered lower post / lower emoluments on the recommendation of the Selection Committee.  f) Age and other relaxations for direct recruits and departmental candidates: 1. By five years for candidates belonging to SC/ST communities.  2. By three years for candidates belonging to OBC communities. 3. For Persons with Benchmark Disabilities (PWBD) falling under the following categories:  (i) UR - ten years, ii) OBC - 13 years (iii) SC/ST - 15 4. Age is relaxable for Central Government servants up to five years in accordance with the instructions or orders issued by the Central Government, from time-to-time. 5. There is no upper age limit for the Institute employees who are treated as departmental candidates.  g) All results will be published on our website and all future communications will be only through email  h) In case a large number of applications are received, screening will be done to limit the number of candidates to those possessing higher/relevant qualification and experience.  i) With regard to any provisions not covered in this notification, the bye laws of THSTI / Govt. ofIndia rules / guidelines shall prevail.  j) Canvassing wrong in any form will be a disqualification.  k) The candidate may be transfer to site location as per the project requirement and management discretion.

How to Apply 1. Documents to be kept handy before filling up the online application: (all the documents except (i) should be in pdf format):  i) A soft copy of your passport size photo and signature. (jpeg/jpg/png format)  ii) A comprehensive CV containing details of qualification, positions held, professional experience / distinctions etc.  iii) Matriculation certificate (equivalent to 10th Standard) / Mark sheet  iv) Intermediate certificate (equivalent to 12th Standard) / Mark sheet  v) Graduation/Diploma degree certificate / Mark sheet  vi) Post-Graduation degree certificate & Mark sheet (if applicable)  vii) PhD/MD Degree (if applicable)  viii) Relevant experience certificates (if applicable)  ix) Caste / Disability certificate in the format prescribed by the Govt. of India, if applicable.  x) Forwarding letter / NOC from the current employer in the case of candidates working in Govt. / PSUs / autonomous bodies.

Procedure for filling up online application : i) The eligible and interested candidates may apply online at the Institute’s website  thsti.res.in/en/Jobs. Applications through any other mode will not be accepted.  ii) The following will be the step wise procedure-  A) Step 1 : Details of applicant  B) Step 2 : Uploading of documents  C) Step 3 : Payment of application fee  • The payment can be made by using Debit Card / Credit Card / Internet Banking /UPI.  • Once payment is made, no correction / modification is possible  • Candidates are requested to keep a copy of the provisional receipt for future reference.  • Fee once paid shall not be refunded under any circumstances.  • Details of fees to be paid are as shown below : 1. Unreserved, OBC & EWS candidates : Rs. 590/- 2. SC/ST/Women/PwBD : Rs 118/- D) Step 4 : Submission of application form.  iii) On successful submission of application, an auto-generated email containing the reference number will be sent to the email address provided. Please keep a note of the reference number for future correspondence.  iv) Candidates are required to keep a printout of the online application form by using the print button on the dashboard for future reference.  v) Candidates must ensure that he / she fulfils all the eligibility criteria as stipulated in the advertisement. If it is found that he / she does not fulfil the stipulated criteria during the recruitment process, the candidature of the candidate will be cancelled. If the same is noticed after the appointment, the candidate will be terminated following due process.  vi) Incomplete applications shall be summarily rejected and no correspondence in this regard shall be entertained.  vii) In case of difficulty in filling up the online form, please send e-mail to [email protected] along with the screenshot of the error displayed (if any)

Last date of receipt of online application : 01st September 2024. The application will be scrutinized/shortlisted and processed for further selection.  SUBMISSION OF APPLICATION WILL BE THRU ONLINE MODE ONLY OTHERWISE IT WILL GET REJECTED OR IGNORED.

Apply Online

Recruitment notice no.: THS-C/RN/17/2024

See All    Ph.D Alerts    M.Pharm Alerts      B.Pharm Alerts    Faridabad Alerts See All   Other Jobs   in our Database Subscribe to Pharmatutor Job Alerts by Email  

RECOMMENDED POSTS

Subscribe with us

Do Not Forget to Verify

(Click on Subscription link in your inbox)

Jobs by Category

Production Jobs

R&D Jobs

F&D Jobs

Sales & Marketing

QC Jobs

Faculty Jobs

Packaging Alerts

Hospital Pharmacist

• Pharma News
• Pharmapedia

Clinical Research Lead Scientist Salary in the United States

Clinical research lead scientist salary, how much does a clinical research lead scientist make.

Last Updated on July 29, 2024

• Paid Annually
• Paid Monthly
• Paid Semimonthly
• Paid Biweekly
• Paid Weekly
• Paid Hourly

Average Salary

Clinical Research Nurse (Day shift)

Celerion - Lincoln, NE

Senior Research Scientist - Adversarial Machine Learning

Carnegie Mellon University - Pittsburgh, PA

CBDI Clinical Research Ops Mgr

Johns Hopkins Medicine - Saint Petersburg, FL

Registered Nurse Pediatric Clinical Research

Professional Case Management - Uvalde, TX

• View Hourly Wages
• Select State
• Select City
• Choose Similar Job
• Pick Related Category
• View Cost of Living in Major Cities

Analyze the market and your qualifications to negotiate your salary with confidence.

Search thousands of open positions to find your next opportunity.

Individualize employee pay based on unique job requirements and personal qualifications.

Get the latest market price for benchmark jobs and jobs in your industry.

View Clinical Research Lead Scientist Salary by Hour, Week, Month, Year

Salary.com provides you with accurate and diversified Clinical Research Lead Scientist salary data based on specialized databases to help you get a fairer salary. Click the switch button below to see more details about Clinical Research Lead Scientist hourly pay, weekly pay, monthly pay and so on.

View Clinical Research Lead Scientist Salary by Experience Levels

An entry-level Clinical Research Lead Scientist with under 1 year experience makes about $92,539. With less than 2 years of experience, a mid-level Clinical Research Lead Scientist makes around $93,666. After 2-4 years, the Clinical Research Lead Scientist pay rises to about $97,722. Those senior Clinical Research Lead Scientist with 5-8 years of experience earn roughly $106,912, and those Clinical Research Lead Scientist having 8 years or more experience are expected to earn about $110,870 on average.

View Clinical Research Lead Scientist Salary by States

Not the salary data you are looking for? Choose the state salary you want to see.

Connecticut

District of Columbia

Massachusetts

Mississippi

North Carolina

North Dakota

New Hampshire

Pennsylvania

Rhode Island

South Carolina

South Dakota

West Virginia

What Am I Worth?

Highest Paying Cities for Clinical Research Lead Scientist

Not the salary data you are looking for? Choose the city salary you want to see.

San Jose, CA

San Francisco, CA

Oakland, CA

New York, NY

Queens Village, NY

Paramus, NJ

Passaic, NJ

Bergenfield, NJ

Stamford, CT

Huntington, NY

Bridgeport, CT

View Clinical Research Lead Scientist Salary Trends

For those exploring the changing dynamics of Clinical Research Lead Scientist salaries, Salary.com offers detailed insights through our Job Trending in CA Labor Market analysis. Our research highlights a notable shift in Clinical Research Lead Scientist compensation over the past six years. For instance, the median salary has moved from $87,046 in 2023 to about $85,583 in 2024 (for a comprehensive analysis of Clinical Research Lead Scientist salary trends, click here). It's crucial to consider several elements, including geographical location, experience level, industry demand, and economic development, as they play a significant role in influencing salary variations.

Average Annual Salary of Clinical Research Lead Scientist Over Time

Clinical research lead scientist salary by year.

Salaries of Jobs Related to Clinical Research Lead Scientist

AI Research Scientist II

AI Research Scientist IV

Associate Clinical Research Scientist

Clinical Research Lead

Clinical Scientist

Lead Clinical Research Associate

Lead Clinical Research Coordinator

Lead Clinical Scientist

Lead Scientist

Scientist - Clinical Research

Senior Scientist Clinical Research

Job Openings of Clinical Research Lead Scientist

Salary.com job board provides millions of Clinical Research Lead Scientist information for you to search for. Click on search button below to see Clinical Research Lead Scientist job openings or enter a new job title here.

Lincoln, NE

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative res... more

4 Months Ago

Carnegie Mellon University

Pittsburgh, PA

At the SEI AI Division, we conduct research in applied artificial intelligence and the engineering questions related to the practical design and implementa... more

0 Months Ago

Johns Hopkins Medicine

Saint Petersburg, FL

Job Description. Job Description. CBDI (Cancer & Blood Disorders Institute) Clinical Research Operations Manager. Johns Hopkins All Children's Hospital is ... more

Professional Case Management

Job Description. Make a Difference on Your Own Schedule and Terms. . Summary. . The Certified Mobile Research Nurse is a Registered Nursing per diem/PRN po... more

15 Days Ago

Memorial Health University Medical Center

Savannah, GA

Description. Introduction. Last year our HCA Healthcare colleagues invested over 156,000 hours volunteering in our communities. As a(an) Clinical Research ... more

Common Company Salaries for Clinical Research Lead Scientist

Here are companies hiring for Clinical Research Lead Scientist and their salaries, click below for more details.

VCA Hospitals

All Industries

BrightView Holdings Inc

Star therapeutics inc, narrow lane co, anteater pest & lawn services, happy tails veterinary hospital, most common benefits for clinical research lead scientist.

If your compensation planning software is too rigid to deploy winning incentive strategies, it’s time to find an adaptable solution.

Clinical Research Lead Scientist Bonus and Incentive Rates

Employers: Find Surveys For This Job

Employers: Price Your Company Jobs

Employees: Get a Salary Increase

Clinical Research Lead Scientist Salary by Educational Level

Salaries for clinical research lead scientist with a high school diploma or technical certificate.

According to our 100% employer reported salary sources the median salary for a Clinical Research Lead Scientist with a JD, MD, PhD or Equivalent is $94,793 - $104,476. Please try our salary wizard to explore how other factors like location, Years of experience and number of direct reports can impact your base pay and bonus.

Clinical Research Lead Scientist Salaries by Degree Level

FAQ about Clinical Research Lead Scientist

1. what are the responsibilities of clinical research lead scientist.

The Clinical Research Lead Scientist proposes, plans, organizes and executes experiments and research. Assumes lead role in various clinical research projects. Being a Clinical Research Lead Scientist summarizes findings in reports and communicates results. Secures grants and funding for research and is responsible for controlling budgets. In addition, Clinical Research Lead Scientist interacts with other scientists within and outside of the organization. Provides recommendations that influence extensive clinical research activities. Requires an advanced degree. Typically reports to head of a unit/department. Being a Clinical Research Lead Scientist work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. Working as a Clinical Research Lead Scientist typically requires 4 -7 years of related experience.

2. What are the skills of Clinical Research Lead Scientist

Specify the abilities and skills that a person needs in order to carry out the specified job duties. Each competency has five to ten behavioral assertions that can be observed, each with a corresponding performance level (from one to five) that is required for a particular job.

Analysis: Analysis is the process of considering something carefully or using statistical methods in order to understand it or explain it.

SOP: SOP is A standard operating procedure is a set of step-by-step instructions compiled by an organization to help workers carry out routine operations.

Process Development: Process development consists of designing and developing, as well as evaluating costs and efficiency.

About Our Data

Salary.com's CompAnalyst platform offers:

• Detailed skills and competency reports for specific positions
• Job and employee pricing reports
• Compensation data tools, salary structures, surveys and benchmarks.

Is this useful?

• Current USC Employees
• Returning Candidates

Search all jobs

Areas Of Work Select Administrative Operations Auxiliary Services Faculty Human Resources Information Technology Keck Medicine of USC

Employment Type Select Faculty Full Time Faculty Part Time Staff Full Time Staff Part Time

Let’s change the world together!

USC is a leading private research university located in Los Angeles – a global center for arts, technology and international business. As one of the city’s largest private employers, responsible for more than $8 billion annually in economic activity in the region, we offer the opportunity to work in a dynamic and diverse environment, in careers that span a broad spectrum of talents and skills across a variety of academic schools and units. As a USC employee, you will enjoy excellent benefits and perks , and you will be a member of the Trojan Family - the faculty, staff, students and alumni who make USC a great place to work. Think you’ve got what it takes to join us? We invite you to search our open positions and apply!

Clinical Research Data Specialist I

The University of Southern California (USC), founded in 1880, is the largest private employer in the City of Los Angeles. As an employee of USC, you will be a part of a world-class research university and a member of the “Trojan Family,” which is comprised of the faculty, students and staff that make the university what it is.

The USC Institute of Urology is seeking for a part-time clinical research data specialist I to facilitate and manage the urologic clinical data for assigned protocols.  The clinical research data specialist I ensures data is documented and recorded as appropriate reads and understands urological clinical data from medical records.  Extracts and enters required clinical data from medical records and patient research charts/reports to Clinical Research Forms (eCRFs/CRFs).  Notifies Principal Investigator (PI) or Study Coordinator of issues or violations. Provides timely data entry.  Addresses all data queries for resolution.  Maintains currency of federal regulations governing the protection of human subjects.  Reports serious adverse events (SAEs) to Study Coordinator and to various agencies, as required.  Assists Clinical Research Data Specialists in reporting SAEs and assessing protocol violations.  Ensures Urology data is available per contract obligations at time of monitoring visits.  Prepares and participates in audits of assigned studies.  Reviews assigned patient charts and reports results.  Assists Study Coordinator with eligibility work-ups for new potential research subjects.  Participates in Quality Assurance Monitoring Committee (QAMC) in-house audits by reviewing assigned patient chart and reporting on findings as relates to protocol/patient compliance.  Ensures confidentiality, accuracy, security and appropriate access of all data and records.

The hourly base salary for this position is $27.92 - $32.13. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal peer equity, federal, state, and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations.

Job matching

With just one click and a connection to LinkedIn, we can connect you with jobs that match your work experience.

Stay connected with University of Southern California

Sign up to receive job alerts

Job Category

Email Address

LinkedIn Profile

Confirm Email

Recently added jobs

• Scheduler - LV Nellis Family Medicine Clinic - Full Time 10 Hour Days (Non-Exempt) (Non-Union) Las Vegas, Nevada REQ20152021
• Assistant/Associate Professor of Clinical Dentistry (OPEN RANK) Los Angeles, California REQ20153549
• Research Programmer I Los Angeles, California REQ20153207

Clinical Research Coordinator Associate

🔍 school of medicine, stanford, california, united states.

The Clinical Research Coordinator Associate is responsible for the overall management and implementation of an assigned set of multiple research protocols assuring efficiency and regulatory compliance. These studies will be conducted at the Stanford Hospital and Clinics. He/she will work as part of a clinical trials research team and report to various Principal Investigators conducting clinical research. Responsibilities include preparation of initial study documents for IRB submission in compliance with all local, state and federal regulations; advise the IRB of amendment changes to the protocol and complete annual protocol renewals. Recruit, screen, assist in the informed consent process and enroll subjects in accordance with good clinical practice guidelines. Collect, record and maintain complete data files using good clinical practice in accordance to HIPAA regulations. He/she participates in data retrieval, reporting, and preparation of files and Case Report Forms for the various studies. The successful candidate will interact with subjects by scheduling diagnostic and research evaluation visits, perform study related assessments including collection of blood samples, processing and shipment. Maintain drug accountability, adequate study supplies and equipment. The coordinator will oversee subject compliance to the study protocol, obtain information from the study subject regarding any changes in their medications or adverse events and promptly report the findings to physicians for documentation in the subject’s medical record. Report all serious adverse events promptly to investigators, sponsors and the IRB. Protect the rights, safety and well-being of human subjects involved in the clinical trials. 

Duties include*:

• Serve as primary contact with research participants, sponsors, and regulatory agencies.  Coordinate studies from startup through close-out.
• Determine eligibility of and gather consent from study participants according to protocol.  Assist in developing recruitment strategies.
• Coordinate collection of study specimens and processing.
• Collect and manage patient and laboratory data for clinical research projects.  Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms. 
• Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents.  Prepare regulatory submissions, and ensure institutional Review Board renewals are completed.
• Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
• Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.
• Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct. 
• Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
• Participate in monitor visits and regulatory audits. 

* - Other duties may also be assigned

EDUCATION & EXPERIENCE (REQUIRED):

Two year college degree and two years related work experience or a Bachelor’s degree in a related field or an equivalent combination of related education and relevant experience. 

KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):

• Strong interpersonal skills.
• Proficiency with Microsoft Office.
• Knowledge of medical terminology.

CERTIFICATIONS & LICENSES:

Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. 

PHYSICAL REQUIREMENTS*:

• Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping. 
• Occasionally sit, reach above shoulders, perform desk based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.
• Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more.

* - Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job. WORKING CONDITIONS: 

Occasional evening and weekend hours.

WORK STANDARDS:

• Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations.
• Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned.
• Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide, http://adminguide.stanford.edu .

The expected pay range for this position is $31.73 to $36.54 per hour.

Stanford University provides pay ranges representing its good faith estimate of what the university reasonably expects to pay for a position. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location and external market pay for comparable jobs.

At Stanford University, base pay represents only one aspect of the comprehensive rewards package. The Cardinal at Work website ( https:/lcardinalatwork.stanford.edu/benefits-rewards ) provides detailed information on Stanford's extensive range of benefits and rewards offered to employees. Specifics about the rewards package for this position may be discussed during the hiring process.

Consistent with its obligations under the law, the University will provide reasonable accommodations to applicants and employees with disabilities. Applicants requiring a reasonable accommodation for any part of the application or hiring process should contact Stanford University Human Resources at [email protected]. For all other inquiries, please submit a contact form .

Stanford is an equal employment opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.

The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory of all duties, tasks, and responsibilities. Specific duties and responsibilities may vary depending on department or program needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned.

• Schedule: Full-time
• Job Code: 1013
• Employee Status: Regular
• Requisition ID: 104161
• Work Arrangement : Hybrid Eligible

My Submissions

Track your opportunities.

Similar Listings

 School of Medicine, Stanford, California, United States

📁 Research

Post Date: Jan 29, 2024

Post Date: Aug 05, 2022

Post Date: Mar 11, 2022

Global Impact We believe in having a global impact

Climate and sustainability.

Stanford's deep commitment to sustainability practices has earned us a Platinum rating and inspired a new school aimed at tackling climate change.

Medical Innovations

Stanford's Innovative Medicines Accelerator is currently focused entirely on helping faculty generate and test new medicines that can slow the spread of COVID-19.

From Google and PayPal to Netflix and Snapchat, Stanford has housed some of the most celebrated innovations in Silicon Valley.

Advancing Education

Through rigorous research, model training programs and partnerships with educators worldwide, Stanford is pursuing equitable, accessible and effective learning for all.

Working Here We believe you matter as much as the work

I love that Stanford is supportive of learning, and as an education institution, that pursuit of knowledge extends to staff members through professional development, wellness, financial planning and staff affinity groups.

School of Engineering

I get to apply my real-world experiences in a setting that welcomes diversity in thinking and offers support in applying new methods. In my short time at Stanford, I've been able to streamline processes that provide better and faster information to our students.

Phillip Cheng

Office of the Vice Provost for Student Affairs

Besides its contributions to science, health, and medicine, Stanford is also the home of pioneers across disciplines. Joining Stanford has been a great way to contribute to our society by supporting emerging leaders.

Denisha Clark

School of Medicine

I like working in a place where ideas matter. Working at Stanford means being part of a vibrant, international culture in addition to getting to do meaningful work.

Office of the President and Provost

Getting Started We believe that you can love your job

Join Stanford in shaping a better tomorrow for your community, humanity and the planet we call home.

• 4.2 Review Ratings
• 81% Recommend to a Friend

View All Jobs