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Clinical Study Start Up Associate Jobs (NOW HIRING)

Tempus

Study Start-Up Specialist

$55K - $70K/yr

... study start-up related questions ... Coordinate with TIME sites and sponsor teams to activate clinical trials through the JIT and ...

Medpace, Inc.

Study Start-Up Intern

Cincinnati, OH

Job Summary Our clinical operations activities are growing rapidly, and we are seeking a full-time, ... Medpace training programs are curated to educate and support experienced associates, as well as ...

Prometrika LLC

Clinical Trial Associate II

Cambridge, MA · On-site

$75K - $90K/yr

The Clinical Trial Associate II (CTA II) supports, coordinates, and implements clinical research ... With minimal oversight, manage all study start up, maintenance and closeout site management ...

BeiGene USA

Regional Clinical Study Senior Manager

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 ...

Global Channel Management, Inc.

$57/hr

Candidates with a nursing diploma/assoc degree with substantial experience may be considered for ... Develop project cross-functional, integrated study plan to study start up (in-house) and validate ...

Icon plc

Clinical Operations Specialist

Raleigh, NC · On-site

As a Study Start Up Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatments ...

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Clinical Study Start Up Associate information

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How much do clinical study start up associate jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for clinical study start up associate in the United States is $31.54, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $41.59 per hour, depending on experience, location, and employer.

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Study Start-Up Specialist

Chicago, IL • On-site

Tempus
See more jobs at Tempusexternal

$55K - $70K/yr

Full-time

Re-posted 10 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.

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