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Internship Clinical Study Startup Jobs (NOW HIRING)

Celldex Therapeutics

Director, Clinical Science

Hampton, NJ · On-site

  • Medical

  • Retirement

  • PTO

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

Novocure

Clinical Trial Lead

Boonton, NJ · Hybrid

$147K - $190K/yr

Lead cross-functional Clinical Study Teams from study startup through closeout. * Serve as the primary liaison between Novocure and CRO partners. * Oversee study timelines, milestones, deliverables ...

Novocure

Clinical Trial Lead

Philadelphia, PA · Hybrid

$147K - $190K/yr

Lead cross-functional Clinical Study Teams from study startup through closeout. * Serve as the primary liaison between Novocure and CRO partners. * Oversee study timelines, milestones, deliverables ...

Novocure

Clinical Trial Lead

Newark, NJ · Hybrid

$147K - $190K/yr

Lead cross-functional Clinical Study Teams from study startup through closeout. * Serve as the primary liaison between Novocure and CRO partners. * Oversee study timelines, milestones, deliverables ...

Novocure

Clinical Trial Lead

Wayne, PA · Hybrid

$147K - $190K/yr

Lead cross-functional Clinical Study Teams from study startup through closeout. * Serve as the primary liaison between Novocure and CRO partners. * Oversee study timelines, milestones, deliverables ...

Novocure

Clinical Trial Lead

Manhattan, NY · Hybrid

$147K - $190K/yr

Lead cross-functional Clinical Study Teams from study startup through closeout. * Serve as the primary liaison between Novocure and CRO partners. * Oversee study timelines, milestones, deliverables ...

Novocure

Clinical Trial Lead

Wayne, PA · On-site

$147K - $190K/yr

Lead cross-functional Clinical Study Teams from study startup through closeout. * Serve as the primary liaison between Novocure and CRO partners. * Oversee study timelines, milestones, deliverables ...

BeiGene USA

Senior Clinical Research Associate

$105K - $140K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Senior Clinical Research Associate (SCRA) is primarily a site monitor and is responsible for ... study startup, recruitment, database analyses, closeout, etc.). Provide support for study sites ...

BeiGene, Inc.

Senior Clinical Research Associate

$105K - $140K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... e., study startup, recruitment, database analyses, closeout, etc.). • Provide support for study sites, and CRAs with audits/inspections preparation/responses and quality issues, as needed, and ...

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Internship Clinical Study Startup information

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How much do internship clinical study startup jobs pay per month?

As of Aug 16, 2026, the average monthly pay for internship clinical study startup in the United States is $6,439.50, according to ZipRecruiter salary data. Most workers in this role earn between $4,416.67 and $7,666.67 per month, depending on experience, location, and employer.

What is the difference between Internship Clinical Study Startup vs Clinical Research Coordinator?

AspectInternship Clinical Study StartupClinical Research Coordinator
CredentialsTypically pursuing or recent graduate, some may have certificationsOften requires a bachelor's degree in health or life sciences, certifications preferred
Work EnvironmentInternship setting, learning-focused, often in clinical trial startup phaseFull-time role in clinical sites or research organizations, managing ongoing studies
Employer & Industry UsagePharmaceutical companies, CROs, academic institutions during trial initiationHospitals, research centers, pharmaceutical companies during study conduct

While an Internship Clinical Study Startup is an entry-level, learning-focused position often held by students or recent graduates, a Clinical Research Coordinator is a more experienced role responsible for managing and overseeing clinical trials throughout their lifecycle. The internship provides foundational exposure, whereas the coordinator role involves active study management and compliance.

What are the key skills and qualifications needed to thrive as an internship in clinical study startup?

To thrive as an Internship Clinical Study Startup, you need a basic understanding of clinical research principles, regulatory requirements, and strong organizational skills, often supported by enrollment in a life sciences or health-related degree program. Familiarity with clinical trial management systems (CTMS), electronic document management tools, and Microsoft Office is typically expected. Attention to detail, effective communication, and a collaborative mindset are crucial soft skills for this role. These skills and qualities are essential for ensuring smooth study initiation, regulatory compliance, and effective teamwork in a dynamic research environment.

What does an internship in clinical study startup involve?

An Internship in Clinical Study Startup typically involves assisting with the early phases of clinical trial preparation, including regulatory documentation, site selection, study feasibility, and ethics submissions. Interns may support communication between clinical sites and sponsors, help organize trial materials, and ensure compliance with regulatory requirements. The role provides exposure to the clinical research process and helps interns develop practical skills in project management, data handling, and teamwork within the pharmaceutical or healthcare industry.

What types of projects and responsibilities can I expect during an internship in clinical study startup?

As an intern in Clinical Study Startup, you'll typically assist with tasks such as drafting study documents, helping prepare regulatory submissions, and coordinating with cross-functional teams like regulatory affairs, site management, and data management. You'll gain hands-on experience in tracking study milestones, collecting essential site documents, and supporting site activation activities. This role often involves close collaboration with mentors and exposure to industry-standard tools, providing a strong foundation for a future career in clinical research.

What cities are hiring for Internship Clinical Study Startup jobs?

Cities with the most Internship Clinical Study Startup job openings:

What are the most commonly searched types of Clinical Study Startup jobs?

The most popular types of Clinical Study Startup jobs are:

What states have the most Internship Clinical Study Startup jobs?

States with the most job openings for Internship Clinical Study Startup jobs include:

Internship Clinical Study Startup jobs near you

Director, Clinical Science

Celldex Therapeutics

Hampton, NJ • On-site

Other

Medical, Retirement, PTO

Posted 9 days ago

Job description

Overview
The Director, Clinical Science is a strategic scientific leader responsible for clinical study design, clinical data review, and execution of clinical development programs supporting innovative therapies. This individual will play a central role in translating scientific and medical insights into robust clinical studies and development strategies, while leading the interpretation of clinical data to inform key program decisions.
Working closely with Clinical Science physicians, Clinical Operations, Data Management, Biostatistics, Regulatory Affairs, Medical Writing, Biomarker/Translational Research, Pharmacovigilance, and Medical Affairs, the Director, Clinical Science will provide leadership across all phases of development, with particular emphasis on protocol development and study design, data review and interpretation, and data-driven decision making.
Responsibilities
Clinical Study Design and Development Strategy
  • Lead the design and development of clinical study protocols, protocol amendments, and associated study documents across all phases of development.
  • Partner with Clinical Science physicians and cross functional stakeholders to define study objectives, endpoints, eligibility criteria, study procedures and visit schedule, safety monitoring plans, and statistical considerations.
  • Ensure study designs are scientifically rigorous, operationally feasible, and aligned with regulatory and development objectives.
  • Contribute to clinical development plans, indication expansion strategies, and overall asset development decisions.
  • Integrate translational, biomarker, pharmacokinetic/pharmacodynamic (PK/PD), and patient-centered endpoints into clinical development programs.
  • Evaluate emerging scientific, competitive, clinical, and regulatory information to inform development strategies.

Clinical Data Review and Interpretation
  • Lead ongoing review and interpretation of clinical trial data, including efficacy, safety, biomarker, PK/PD, immunogenicity, and patient-reported outcomes.
  • Develop and implement data review strategies in collaboration with Biostatistics and Data Management.
  • Identify emerging trends, clinical signals, and development risks and provide recommendations to study teams and senior leadership.
  • Lead clinical review meetings and contribute to study conclusions, integrated analyses, and clinical development recommendations.
  • Present clinical data and program updates to governance committees, senior management, and cross-functional teams.
  • Support benefit-risk assessments and key development decisions throughout the product lifecycle.

Clinical Trial Execution and Scientific Oversight
  • Serve as the Clinical Science lead for assigned studies and development programs.
  • Provide scientific oversight during study conduct to ensure high-quality execution and data integrity.
  • Collaborate with Clinical Operations to support study startup, enrollment, protocol adherence, and issue resolution.
  • Participate in investigator meetings, advisory boards, and interactions with key opinion leaders and external experts.
  • Contribute to inspection readiness and compliance with GCP, ICH guidelines, and applicable regulatory requirements.

Regulatory and Scientific Contributions
  • Author and review clinical sections of regulatory documents, including INDs, CTAs, Investigator Brochures, Clinical Study Reports, briefing packages, periodic safety reports, annual reports, and marketing applications.
  • Support interactions with global health authorities and responses to regulatory inquiries.
  • Collaborate with Regulatory Affairs and Medical Writing to ensure high-quality and compliant clinical documentation.
  • Contribute to scientific publications, abstracts, posters, presentations, and congress materials.

Cross-Functional Leadership
  • Partner closely with Clinical Science physicians, Data management, Biomarker/Translational Research, Clinical Operations, Biostatistics, Safety, Regulatory Affairs, Medical Writing, and Medical Affairs.
  • Represent Clinical Science on cross-functional project teams, governance committees, and portfolio discussions.
  • Drive alignment across functions to support efficient decision-making and program execution.
  • Mentor and develop Clinical Scientists and contribute to building a culture of scientific excellence and continuous improvement.

Qualifications
  • Advanced degree in a scientific, healthcare, or related discipline preferred (e.g., PhD, PharmD, MD, DO, MS, MPH, NP, PA, or equivalent).
  • 10+ years of clinical research, clinical development, or clinical science experience within the biotechnology, pharmaceutical, or CRO industry.
  • Demonstrated experience leading clinical study design, protocol development, and clinical data review activities.
  • Experience serving as Clinical Science Lead for Phase 1 through Phase 3 clinical trials.
  • Proven track record of interpreting complex clinical datasets and translating findings into development strategy.
  • Experience supporting regulatory submissions and health authority interactions.
  • Experience in Immunology, autoimmune diseases, inflammatory disorders, or related therapeutic areas strongly preferred.
  • Biotechnology industry experience preferred.
  • Deep understanding of clinical trial methodology, study design, endpoint development, and statistical concepts.
  • Expertise in clinical data review and interpretation of efficacy, safety, biomarker, PK/PD, and translational data.
  • Strong knowledge of GCP, ICH guidelines, and global regulatory requirements.
  • Excellent scientific writing, communication, and presentation skills.
  • Strategic thinker with strong scientific judgment and analytical skills.
  • Proven ability to influence cross-functional teams and senior stakeholders.
  • Strong leadership, collaboration, and decision-making capabilities.
  • Ability to thrive in a fast-paced, innovative biotechnology environment.

Compensation Statement
The expected base salary for this position is: $176659.00 to $229427.00. We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market.
Compensation for this role includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page
Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach.

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