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Full Time Clinical Study Start Up Jobs (NOW HIRING)

Study Start-Up Coordinator- PhD

Cincinnati, OH · On-site +1

  • Medical

  • Retirement

  • PTO

Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Regulatory Submissions Coordinators to join our Study Start-up team. This ...

Regional Clinical Study Associate Manager

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Generates, manages, and maintains high quality study start up and recruitment timelines for region and tracks progress towards these * Ensures that the clinical study is operationally feasible in the ...

Study Start-Up Project Manager

Irving, TX · On-site +1

  • Medical

  • Retirement

  • PTO

Our clinical operations activities are growing rapidly, and we are currently seeking a full-time Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays a ...

Regional Clinical Study Senior Manager

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Generates, manages, and maintains high quality study start up and recruitment timelines for region and tracks progress towards these * Ensures that the clinical study is operationally feasible in the ...

Study Start-Up Project Manager

Cincinnati, OH · On-site +1

  • Medical

  • Retirement

  • PTO

Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays ...

Regional Clinical Study Manager

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Generates, manages, and maintains high quality study start up and recruitment timelines for region and tracks progress towards these * Ensures that the clinical study is operationally feasible in the ...

Primary Function of the Position This position requires a candidate with extensive experience with planning, study start-up, and execution of clinical studies. This Lead Clinical Study Manager-4 (CSM ...

Showing results 21-40

Full Time Clinical Study Start Up information

See salary details

$22K

$125.3K

$206K

How much do full time clinical study start up jobs pay per year?

As of Aug 14, 2026, the average yearly pay for full time clinical study start up in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.

What is the difference between Full Time Clinical Study Start Up vs Clinical Research Coordinator?

AspectFull Time Clinical Study Start UpClinical Research Coordinator
ResponsibilitiesPlanning, site selection, regulatory submissions, startup documentationParticipant recruitment, data collection, site coordination
CredentialsTypically requires a degree in health sciences or related field, experience in study startupOften requires a degree or certification in health or research, with focus on coordination
Work EnvironmentOffice-based, regulatory and planning focusSite-based, patient interaction and data management

Full Time Clinical Study Start Up professionals focus on preparing and initiating clinical trials, handling regulatory and site setup tasks. Clinical Research Coordinators primarily manage participant interactions and data collection at study sites. Both roles require related credentials but differ in daily responsibilities and work environment.

More about Full Time Clinical Study Start Up jobs

What cities are hiring for Full Time Clinical Study Start Up jobs?

Cities with the most Full Time Clinical Study Start Up job openings:

What are the most commonly searched types of Clinical Study Start Up jobs?

The most popular types of Clinical Study Start Up jobs are:

What states have the most Full Time Clinical Study Start Up jobs?

States with the most job openings for Full Time Clinical Study Start Up jobs include:

What job categories do people searching Full Time Clinical Study Start Up jobs look for?

The top searched job categories for Full Time Clinical Study Start Up jobs are:

Infographic showing various Full Time Clinical Study Start Up job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 64% Full Time, 16% Part Time, and 19% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $125,290 per year, or $60.2 per hour.

Study Start-Up Specialist

Tempus

Chicago, IL • On-site

$55K - $70K/yr

Full-time

Posted 13 days ago


Job description

Passionate about precision medicine and advancing the healthcare industry?
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.
Responsibilities:
  • Act as the single point of contact from Tempus for JIT and expedited site activations, including maintaining site activation timelines and answering study start-up related questions.
  • Coordinate with TIME sites and sponsor teams to activate clinical trials through the JIT and expedited activation process in order to enroll eligible patients.
  • Collaborate with the central IRB team to facilitate IRB review and approval.
    • Attend bi-weekly meetings with the central IRB team
  • Educate TIME sites and sponsor partners on the JIT and expedited activation processes and best practices.
    • Attend Rapid Activation Demos for onboarding TIME sites
    • Attend standing meetings with TIME sites to review site activation process and ongoing activations
    • Attend sponsor KOMs (where applicable)
    • Attend standing meetings with sponsors to review ongoing site activations (where applicable)
  • Contribute to relationships with TIME sites and pharmaceutical/ CRO partners in the TIME program.
  • Support the team performing feasibility, activations, and other activities within the start up processes.
  • Develop and implement new products, services, and workflows to drive efficiencies throughout the SSU and TIME team.
    • Contribute to the development of marketing collateral for the TIME program.
  • Administrative tasks associated with the activities listed above.

Minimum Qualifications:
  • Bachelor's degree in science or health related field.
  • 2+ years of experience working as a clinical research coordinator in oncology or experience working for a pharmaceutical company/CRO.
  • Deep understanding of study start-up and site activation.
  • Knowledge of current FDA regulations, Good Clinical Practices governing clinical research, and HIPAA compliance.
  • Strong project management skills, with the ability to set goals and prioritize and manage multiple projects simultaneously.
  • Excellent organization and written/ oral communication skills with high attention to detail and accuracy.
  • Ability to develop and maintain strong relationships.
  • Superior analytical, interpersonal, and problem-solving skills.
  • CCRC preferable

• • Proficient in the use of MS Office applications (Outlook, Word, Excel, PowerPoint).
#LI-DA1
$55,000-$70,000
The expected salary range may vary for other locations. Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.