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Full Time Clinical Study Startup Jobs (NOW HIRING)

Whoop

Senior Clinical Scientist

Boston, MA · On-site

Support and oversee key aspects of study execution, including feasibility assessment, study startup ... S. base salary range for this full-time position is $145,000 - $195,000. Salary ranges are ...

Novocure

Clinical Trial Lead

Wayne, PA · Hybrid

$147K - $190K/yr

Clinical Trial Lead Hybrid / Full Time / Chesterbrook, PA At Novocure, we're working to extend the ... Lead cross-functional Clinical Study Teams from study startup through closeout. * Serve as the ...

Novocure

Clinical Trial Lead

Philadelphia, PA · Hybrid

$147K - $190K/yr

Clinical Trial Lead Hybrid / Full Time / Chesterbrook, PA At Novocure, we're working to extend the ... Lead cross-functional Clinical Study Teams from study startup through closeout. * Serve as the ...

Novocure

Clinical Trial Lead

Manhattan, NY · Hybrid

$147K - $190K/yr

Clinical Trial Lead Hybrid / Full Time / Chesterbrook, PA At Novocure, we're working to extend the ... Lead cross-functional Clinical Study Teams from study startup through closeout. * Serve as the ...

Celldex Therapeutics

Director, Clinical Science

Hampton, NJ · On-site

$81K - $110K/yr

Collaborate with Clinical Operations to support study startup, enrollment, protocol adherence, and issue resolution. * Participate in investigator meetings, advisory boards, and interactions with key ...

University of Utah

Clinical Study Coordinators

Campus, IL · On-site

$22K - $51K/mo

Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Responsibilities Clinical Study Coordinator, I Helps with the logistical and administrative aspects ...

Pathos

Director, Clinical Science

New York, NY · On-site

$200K - $240K/yr

You own protocol development, data review, clinical document authorship, and site-level scientific support from study startup through closeout. You will work closely with Clinical Operations ...

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How much do full time clinical study startup jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for full time clinical study startup in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What is a full time clinical study startup?

A Full Time Clinical Study Startup role involves overseeing and coordinating the initial phases of clinical trials, such as site selection, regulatory document collection, ethics submissions, and study initiation activities. Professionals in this position ensure that all necessary approvals and documentation are in place to begin the clinical study on schedule. They work closely with clinical research teams, investigators, and regulatory bodies to manage timelines and compliance with applicable guidelines. This role is crucial for ensuring that clinical trials start efficiently and adhere to all regulatory requirements.

What are some common challenges faced during the clinical study startup phase, and how can they be addressed?

One common challenge in clinical study startup roles is coordinating timelines between multiple stakeholders, such as regulatory bodies, ethics committees, and site staff. Delays often occur due to incomplete documentation or differing site requirements. Effective communication, proactive planning, and familiarity with regulatory processes are key to overcoming these obstacles. Working closely with cross-functional teams and maintaining detailed trackers can help ensure a smoother and faster study initiation.

What are the key skills and qualifications needed to thrive as a full time clinical study startup professional, and why are they important?

To thrive as a Full Time Clinical Study Startup professional, you need a strong background in clinical research, regulatory requirements, and project management, often supported by a life sciences degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), regulatory documentation platforms, and Good Clinical Practice (GCP) certification is typically required. Exceptional organizational skills, attention to detail, and effective communication are vital soft skills for coordinating stakeholders and ensuring study timelines are met. These competencies are essential for ensuring the compliant, efficient, and timely initiation of clinical studies.
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Full Time Clinical Study Startup jobs near you
Infographic showing various Full Time Clinical Study Startup job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Senior Clinical Scientist

Whoop

Boston, MA • On-site

Full-time

Posted 16 days ago

Job description

WHOOP is an advanced health and fitness wearable on a mission to unlock human performance. We empower our members to improve their health and perform at a higher level through a deeper understanding of their bodies and daily lives.
As a Senior Clinical Scientist, you will independently own assigned clinical studies that support WHOOP's clinical development, product innovation, and regulatory objectives. Operating with minimal oversight, you will translate clinical and product questions into rigorous research approaches, generate and interpret evidence from clinical, wearable, and real-world data, and communicate findings in a way that informs product decisions, regulatory strategy, and clinical evidence generation. This role requires someone who can lead their assigned workstreams, partner effectively across cross-functional teams.
RESPONSIBILITIES:
  • Independently lead the design and development of clinical study protocols, evidence-generation plans, endpoints, study procedures, and statistical analysis approaches with minimal oversight. Ensure studies are scientifically rigorous and aligned with clinical, product, and regulatory objectives
  • Support and oversee key aspects of study execution, including feasibility assessment, study startup, data collection, data review, monitoring oversight, and study closeout. Partner with Clinical Operations, Data Management, and external vendors or sites as needed to ensure high-quality execution
  • Use statistical tools such as R, SAS, Python, Stata, or similar platforms to analyze clinical, wearable, and real-world datasets. Interpret results, identify trends and limitations, and generate actionable insights that support clinical, regulatory, and product decision-making
  • Conduct comprehensive literature reviews to inform study design, endpoint selection, statistical methodologies, product claims, regulatory strategy, and scientific positioning. Integrate external scientific evidence with WHOOP data to support clinical development goals
  • Ensure the accuracy, integrity, and quality of clinical data by implementing and reviewing appropriate quality control measures throughout the study lifecycle. Conduct quality checks on datasets, statistical outputs, tables, figures, listings, and scientific conclusions
  • Communicate complex clinical and statistical findings in clear, actionable terms to clinical, product, data science, regulatory, and executive stakeholders. Translate technical analyses into meaningful business, product, and clinical insights
  • Independently author and review clinical study reports, protocols, statistical analysis plans, literature reviews, clinical evidence summaries, regulatory submission sections, manuscripts, abstracts, and internal scientific memos. Ensure documentation is accurate, scientifically sound, and regulatory-compliant
  • CWork closely with Product, Data Science, Engineering, Clinical Operations, Regulatory Affairs, Quality, and Legal teams to ensure clinical and scientific input is incorporated throughout the product lifecycle
  • Contribute to evidence-generation strategies and clinical documentation for regulatory submissions, including 510(k), De Novo, CE Mark, clinical evaluation reports, clinical study reports, and responses to regulatory questions
  • Lead or contribute to manuscripts, abstracts, posters, presentations, and other scientific communications for internal stakeholders, scientific conferences, peer-reviewed journals, and external collaborators

QUALIFICATIONS:
  • Advanced degree preferred in Life Sciences, Clinical Research, Public Health, Epidemiology, Biostatistics, Biomedical Engineering, Medicine, or a related field. Master's, PhD, MD, PharmD, MPH, or equivalent experience strongly preferred
  • 6-9 years of experience in clinical research, clinical science, data analysis, epidemiology, medical device, digital health, SaMD, pharmaceutical, biotech, or real-world evidence settings
  • Demonstrated ability to independently design and lead clinical studies, including protocol development, endpoint selection, study methodology, statistical analysis planning, and clinical study report writing
  • Strong understanding of FDA regulations, ICH-GCP, ISO 14155, clinical trial design, and evidence-generation requirements for regulated or health-related products
  • Experience contributing to regulatory submissions or clinical evidence packages, such as 510(k), De Novo, CE Mark, clinical evaluation reports, clinical study reports, or related documentation
  • Proficiency in statistical software such as R, SAS, Python, Stata, or similar tools
  • Strong analytical and problem-solving skills, with the ability to interpret complex datasets and clearly explain findings, limitations, and implications
  • Excellent written and verbal communication skills, including experience writing clinical study reports, regulatory documents, scientific manuscripts, abstracts, presentations, or internal research summaries
  • Ability to independently manage complex work streams, prioritize effectively, and deliver high-quality work in a fast-paced environment with minimal oversight
  • Nice to have: Experience working with clinical data, wearable data, real-world data, observational datasets, or large-scale health datasets
  • Nice to have: Experience with software as a medical device, digital biomarkers, wearable sensors, remote patient monitoring, or consumer health technology
  • Nice to have: Experience with Snowflake or other large-scale data platforms
  • Nice to have: Familiarity with software validation, algorithm validation, and clinical performance evaluation for digital health or SaMD products

This role is based in the WHOOP office located in Boston, MA. The successful candidate must be prepared to relocate if necessary to work out of the Boston, MA office.
Interested in the role, but don't meet every qualification? We encourage you to still apply! At WHOOP, we believe there is much more to a candidate than what is written on paper, and we value character as much as experience. As we continue to build a diverse and inclusive environment, we encourage anyone who is interested in this role to apply.
WHOOP is an Equal Opportunity Employer and participates in E-verify to determine employment eligibility. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
The WHOOP compensation philosophy is designed to attract, motivate, and retain exceptional talent by offering competitive base salaries, meaningful equity, and consistent pay practices that reflect our mission and core values.
At WHOOP, we view total compensation as the combination of base salary, equity, and benefits, with equity serving as a key differentiator that aligns our employees with the long-term success of the company and allows every member of our corporate team to own part of WHOOP and share in the company's long-term growth and success.
The U.S. base salary range for this full-time position is $145,000 - $195,000. Salary ranges are determined by role, level, and location. Within each range, individual pay is based on factors such as job-related skills, experience, performance, and relevant education or training.
In addition to the base salary, the successful candidate will also receive benefits and a generous equity package.
These ranges may be modified in the future to reflect evolving market conditions and organizational needs. While most offers will typically fall toward the starting point of the range, total compensation will depend on the candidate's specific qualifications, expertise, and alignment with the role's requirements.
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About Whoop

Sourced by ZipRecruiter

At WHOOP, we're on a mission to unlock human performance. WHOOP empowers users (Olympians, Professional Athletes, Fitness Enthusiasts, etc) to perform at a higher level through a deeper understanding of their bodies and daily lives.

Industry

Fitness and sports centers

Company size

501 - 1,000 Employees

Headquarters location

Boston, MA, US

Year founded

2012

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