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Clinical Study Lead Jobs (NOW HIRING)

Dyne Therapeutics

Senior Clinical Trial Associate

Waltham, MA · On-site

$36.25 - $49.25/hr

Support the Clinical Study Lead and cross-functional study team across all phases of global clinical trial execution, including feasibility, study planning, start-up, enrollment, maintenance, and ...

ARTHREX

Sr. Clinical Study Manager

Naples, FL · On-site +1

Project lead for other research staff assigned to multicenter studies. * Key decision maker for study amendments and strategies * Maintain appropriate monitoring and maintenance of clinical sites to ...

Arthrex

Clinical Study Manager

Naples, FL · On-site

Clinical Study Manager Arthrex, Inc. is a global medical device company and a leader in new product ... They would also lead contract and budget negotiations, vendor onboarding, site training, and ...

Arthrex

Sr. Clinical Study Manager

Naples, FL · On-site

Project lead for other research staff assigned to multicenter studies. * Key decision maker for study amendments and strategies * Maintain appropriate monitoring and maintenance of clinical sites to ...

Veranex

Senior Clinical Study Manager

San Jose, CA · On-site

$125K - $179K/yr

The Senior Clinical Study Manager is responsible for planning, executing, and overseeing clinical ... Lead day-to-day management of study activities and deliverables. * Serve as a liaison with ...

Intuitive

Sr. Clinical Study Manager

Sunnyvale, CA · On-site +1

We lead with inclusion and empower our team members to do their best work as their most authentic ... The Clinical Study Manager-4 (CSM IV) role will develop and execute strategies for clinical and ...

ARTHREX

Clinical Study Manager

Naples, FL · On-site

Clinical Study Manager Arthrex, Inc. is a global medical device company and a leader in new product ... They would also lead contract and budget negotiations, vendor onboarding, site training, and ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

Organize and lead study meetings and other study activities as assigned * Mentor junior clinical study manager(s); provide guidance to CRAs and CTAs on monitoring and other study needs * Follow ...

Connexion Systems & Engineering, Inc.

Be Seen First

Clinical Study Manager

Durham, NC · On-site

$57 - $71/hr

We are seeking an experienced Clinical Study Manager to lead the operational execution of clinical studies from start-up through close-out. This position is responsible for coordinating study ...

Icon plc

Study Lead Biostatistician

Blue Bell, PA · On-site

Study Lead Biostatistician ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site

This Lead Clinical Study Manager-4 (CSM IV) / Senior Clinical Study Manager role will develop and execute strategies for US and global first-human-use and pivotal pre-market clinical trials to help ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

This Lead Clinical Study Manager-4 (CSM IV) / Senior Clinical Study Manager role will develop and execute strategies for US and global first-human-use and pivotal pre-market clinical trials to help ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

Organize and lead study meetings and other study activities as assigned * Mentor junior clinical study manager(s); provide guidance to CRAs and CTAs on monitoring and other study needs * Follow ...

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Clinical Study Lead information

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$36K

$81.2K

$156K

How much do clinical study lead jobs pay per year?

As of Jul 24, 2026, the average yearly pay for clinical study 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.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, understanding of Good Clinical Practice (GCP), and often a relevant degree. Entry-level roles in clinical research may include Clinical Trial Assistant or Clinical Research Coordinator, with CRAs generally needing several years of experience before advancing to that role.

How does a Clinical Study Lead typically coordinate with cross-functional teams during a clinical trial?

A Clinical Study Lead regularly collaborates with various cross-functional teams, including clinical operations, data management, regulatory affairs, and biostatistics, to ensure the successful execution of clinical trials. They facilitate communication between departments, organize project meetings, and address any operational challenges that arise. By fostering strong relationships and clear communication, the Study Lead helps keep the study on track with timelines, compliance, and quality standards. This role requires proactive problem-solving and adaptability to effectively manage the dynamic environment of clinical research.

What jobs pay $10,000 a week?

In the field of clinical research, senior roles such as Clinical Study Lead or Principal Investigator can earn high weekly salaries, especially with extensive experience, specialized skills, and leadership responsibilities. These positions often require advanced degrees, certifications, and a strong track record in managing complex studies, which can lead to compensation reaching or exceeding $10,000 per week in certain organizations or consulting arrangements.

What is the difference between Clinical Study Lead vs Clinical Research Associate?

AspectClinical Study LeadClinical Research Associate
ResponsibilitiesOversees entire clinical study, manages teams, ensures protocol adherenceMonitors site activities, collects data, ensures compliance at sites
Required CredentialsTypically requires a degree in life sciences, experience in clinical trialsUsually requires a degree or background in health sciences, some certifications
Work EnvironmentLeads study teams, interacts with sponsors, manages multiple sitesWorks at clinical sites, monitors progress, reports to study managers

While both roles are essential in clinical trials, the Clinical Study Lead has a broader leadership and oversight role, whereas the Clinical Research Associate focuses on site monitoring and data collection. Both positions require relevant experience and knowledge of clinical trial processes, but the Study Lead typically has more managerial responsibilities.

What is a clinical study lead?

A clinical study lead is a professional responsible for overseeing the planning, execution, and management of clinical trials to ensure they meet regulatory standards and study protocols. They coordinate with cross-functional teams, monitor progress, and ensure data integrity, often requiring knowledge of Good Clinical Practice (GCP) and relevant software tools.

Is CRA better than CRC?

A Clinical Research Associate (CRA) and a Clinical Research Coordinator (CRC) are different roles in clinical trials. CRAs typically oversee multiple sites, monitor study progress, and ensure compliance, often working remotely or traveling frequently, while CRCs manage day-to-day trial activities at a single site, including patient recruitment and data collection. Both roles require knowledge of Good Clinical Practice (GCP) and relevant certifications, but they differ in scope and responsibilities within the clinical research process.

What are the key skills and qualifications needed to thrive as a Clinical Study Lead, and why are they important?

To thrive as a Clinical Study Lead, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as GCP (Good Clinical Practice) are commonly required. Excellent leadership, organizational, and communication skills help coordinate cross-functional teams and ensure study milestones are met. These skills and qualifications are crucial for maintaining study integrity, meeting regulatory standards, and delivering successful clinical trial outcomes.
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What job categories do people searching Clinical Study Lead jobs look for? The top searched job categories for Clinical Study Lead jobs are:
Clinical Study Lead jobs near you
Infographic showing various Clinical Study Lead job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $81,196 per year, or $39 per hour.
Clinical Study Specialist

Clinical Study Specialist

Regeneron Pharmaceuticals, Inc.

Tarrytown, NY • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 17 days ago

Regeneron rating

8.7

Company rating: 8.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

10th of 74 rated pharmaceutical

Job description

Build our future together:
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Clinical Study Specialist to join our Clinical Trial Management team. In this role, you will provide technical and administrative support to clinical study teams executing trials across a program, helping ensure studies stay on track from site activation through close-out, while collaborating with Clinical Study Leads, Clinical Study Associate Managers, CROs, and study sites.
This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.
When & where:
  • Location: Armonk, NY, Warren, NJ
  • Hybrid; 4 days per week onsite

Discover your role:
  • Organizes and delivers analyzable reports and metrics, and coordinates study team meetings, agendas, and minutes
  • Collates data for feasibility and site selection assessments, and contributes to review of study documents (e.g., informed consent forms, case report forms) and reference materials (e.g., regulatory, pharmacy, laboratory binders)
  • Tracks site activation, enrollment, and monitoring visits against projected plans, escalating issues or delays, and monitors investigator/site status and registry postings
  • Ensures timely receipt of scheduled reports (e.g., 1572s, financial disclosures) and performs TMF reconciliations with study lead guidance
  • Communicates with sites as directed, maintaining site contact information and strong relationships internally and externally
  • Contributes to close-out activities (e.g., 1572s, IP reconciliation, financial disclosures, CRA close-out visits) and supports oversight of third-party vendors as needed
  • Brings attention to detail, resourcefulness, and proactive problem-solving to assigned study activities, investigating impact on trials as new information arises
  • Participates in SOP revisions and departmental initiatives, proactively recommending process improvements

This role requires:
  • Bachelor's degree with 2+ years of industry-related work experience in a clinical setting
  • Ability to acquire working knowledge in trial management systems and MS applications (Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC, TMF)
  • Basic familiarity with medical terms and clinical drug development
  • Awareness of ICH/GCP
  • Proactive, self-disciplined, and effective at managing deadlines and priorities

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about on-site expectations for your role and location.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
For jobs in Canada: this posting is for an existing position.
Salary Range (annually)
$93,900.00 - $153,300.00

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