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Clinical Study Lead Jobs (NOW HIRING)

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Global Study Lead

Blue Bell, PA · Remote

Global Study Lead - Oncology - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...

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Global Study Lead

Blue Bell, PA · Remote

Global Study Lead - Oncology - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...

Mindlance

Clinical Research Assocoate

San Diego, CA

The Position The Clinical Research Associate (CRA) provides support to Study Lead(s) in clinical study planning, execution and management. The primary purpose of the position is to support the COM ...

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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 Jun 12, 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 Assistants or Coordinators, with CRAs generally advancing from these positions or related roles. Certification and training can also be important for career progression as a CRA.

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 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 jobs pay 2000 a day?

High-paying jobs that can pay around $2,000 a day often include specialized roles such as senior clinical study leads, anesthesiologists, surgeons, or senior consultants, typically requiring advanced degrees, certifications, and significant experience. These roles are usually found in healthcare, consulting, or executive positions and may involve project-based or contract work with high hourly or daily rates.

What is a Clinical Study Lead?

A Clinical Study Lead is a professional responsible for overseeing and managing the execution of clinical trials or studies within the pharmaceutical, biotechnology, or medical device industries. Their primary duties include planning, coordinating, and monitoring all aspects of a clinical study to ensure it adheres to regulatory guidelines, timelines, and budgets. They work closely with cross-functional teams, such as clinical research associates, data managers, and regulatory affairs specialists, to ensure the study is conducted efficiently and ethically. Clinical Study Leads also serve as the main point of contact between the sponsor, study sites, and regulatory authorities, ensuring all stakeholders are informed and aligned throughout the trial process.

What is the role of a clinical study lead?

A clinical study lead is 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 quality, often using tools like electronic data capture systems. Strong leadership, regulatory knowledge, and project management skills are essential for this role.

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.

Is a CRC higher than a CRA?

A Clinical Research Coordinator (CRC) and a Clinical Research Associate (CRA) are different roles in clinical trials; a CRA typically has more seniority and oversight responsibilities, often involving monitoring and site management, while a CRC handles patient interactions and data collection at the site level. The CRA usually requires more experience, certifications, and knowledge of regulatory requirements, making it generally a higher or more advanced position in the clinical research hierarchy.
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Clinical Study Lead jobs near you
Infographic showing various Clinical Study Lead job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 97% Full Time, and 2% Part Time. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $81,196 per year, or $39 per hour.
Clinical Study Lead

Clinical Study Lead

Advanced Recruiting Partners

Raleigh, NC

Other

Posted 23 days ago

Job description

Job Summary:

The Study Lead will oversee the planning, execution, and management of clinical trials from start to finish. This role involves coordinating study activities, ensuring compliance with regulatory requirements, and leading a team of CRAs while collaborating closely with cross-functional teams. The ideal candidate will have a strong background in clinical trial management and a passion for advancing medical research.


Key Responsibilities:

  • Lead the planning, execution, and management of clinical trials in accordance with GCP, regulatory guidelines, and company SOPs.
  • Develop and manage study protocols, informed consent forms, and other essential study documentation.
  • Serve as the primary point of contact for all study-related inquiries and issues.
  • Coordinate with site personnel, vendors, and internal teams to ensure smooth study execution.
  • Monitor study progress and conduct regular reviews of study data to ensure integrity and compliance.
  • Provide training and mentorship to CRAs and other study team members.
  • Assist in the selection and evaluation of clinical sites and vendors.
  • Prepare and present study updates to senior management and stakeholders.
  • Participate in regulatory submissions and inspections as needed.
  • Identify and mitigate study-related risks proactively.


Qualifications:

  • Bachelor’s degree in life sciences or a related field; advanced degree preferred.
  • Minimum 3 years of experience in clinical trial management or CRA role, preferably in a biotech environment.
  • Strong understanding of clinical trial regulations and Good Clinical Practice (GCP).
  • Excellent organizational and project management skills.
  • Strong interpersonal and communication skills, with the ability to work collaboratively in a team-oriented environment.
  • Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
  • Ability to work independently and adapt to changing priorities in a fast-paced environment.

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