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Clinical Study Team Lead Jobs (NOW HIRING)

CEDENT

Study Start-Up Manager

Wilmington, DE

Summary We are looking for a Study Start-Up Manager with extensive experience to lead clinical ... Participate in Local Study Team meetings and report on site performance metrics. * Ensure the ...

BeiGene USA

Regional Clinical Study Senior Manager

Acts as regional lead for multiple studies across an indication or across a program as required * Leads the regional clinical operations team (including external partners working on a regional level ...

Kps-Life

Sr. Clinical Study Lead (Hybrid)

Cambridge, MA · On-site

On Assignment Sr. Clinical Study Lead (Hybrid) KPS Life is hiring a Senior Clinical Study Lead (Sr. ... Leads the cross-functional study team responsible for clinical study delivery and is the primary ...

New

ARTHREX

Clinical Study Manager

Naples, FL · On-site

They would also lead contract and budget negotiations, vendor onboarding, site training, and ... Join our talented team at a global medical device company focused on Helping Surgeons Treat Their ...

Zentalis

Sr Clinical Study Manager

San Diego, CA · Remote

We are seeking an experienced and driven Senior Clinical Study Manager to lead the cross-functional Clinical Study Team and ensure successful delivery of assigned clinical studies. In this role, you ...

Arthrex

Clinical Study Manager

Naples, FL · On-site

They would also lead contract and budget negotiations, vendor onboarding, site training, and ... Join our talented team at a global medical device company focused on Helping Surgeons Treat Their ...

Kps-Life

Clinical Study Specialist

Cambridge, MA · On-site

Organize and deliver reports, metrics, and study updates to the Clinical Study Lead. * Schedule and coordinate clinical study team and study-related meetings, including agendas, presentations ...

Global Channel Management, Inc.

$57/hr

Qualifications Clinical Study Manager needs 5 years relevant experience is required with a BSc, 3 ... team and CRO). * Contribute to operational delivery aspects of the protocol and lead document ...

BeiGene USA

Regional Clinical Study Manager

Accountable for regional study delivery with appropriate inspection readiness quality, within ... Proven experience in clinical research including relevant experience as team lead in clinicial ...

BeiGene, Inc.

Regional Clinical Study Manager

Accountable for regional study delivery with appropriate inspection readiness quality, within ... Proven experience in clinical research including relevant experience as team lead in clinicial ...

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Clinical Study Team Lead information

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How much do clinical study team lead jobs pay per year?

As of Sep 12, 2026, the average yearly pay for clinical study team lead in the United States is $81,196.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,000.00 and $90,000.00 per year, depending on experience, location, and employer.

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Infographic showing various Clinical Study Team Lead job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 18% Part Time, and 4% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $81,196 per year, or $39 per hour.

Study Start-Up Manager

Wilmington, DE

CEDENT
IT Services • 11 - 50 employees
Learn more about CEDENTexternal

Full-time

Re-posted 17 days ago

Job description

Summary

We are looking for a Study Start-Up Manager with extensive experience to lead clinical study start-up activities. This role requires a strong background in regulatory processes, site management, and expertise in ensuring compliance with local and international guidelines, particularly ICH-GCP.
 

Key Responsibilities
  • Lead and manage start-up activities for clinical studies, ensuring compliance with local and international guidelines (ICH-GCP).
  • Prepare, review, and track site regulatory documentation throughout the study start-up phase.
  • Collaborate with Clinical Research Associates (CRAs) and the local study team to meet start-up milestones.
  • Participate in Local Study Team meetings and report on site performance metrics.
  • Ensure the timely submission of documents to regulatory authorities and maintain the trial master file (eTMF).

Qualifications
  • Minimum 3 years of experience in Clinical Study Start-Up (full-time).
  • At least 1 year of hands-on experience with Veeva Vault.
  • Strong background in informed consent review and negotiation.
  • Bachelor’s degree (higher degree preferred) with knowledge of clinical trial processes (Phases II-IV) and ICH-GCP.
  • Excellent communication, organizational, and project management skills.
  • Strong problem-solving and negotiation abilities.
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About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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