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Internship Clinical Study Startup Jobs (NOW HIRING)

BeiGene, Inc.

Senior Clinical Research Associate

$105K - $140K/yr

... 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 ...

3ds

VP Professional Services, Study Experience

Iselin, NJ · On-site

$140K - $180K/yr

Serve as the executive subject matter expert on the clinical study lifecycle, from protocol design and study startup to data management, analysis, and close-out. * Ensure all service delivery ...

NWRPros

Clinical Research Associate

Seattle, WA · On-site

$115K - $145K/yr

Our client is an exciting clinical-stage biotechnology company focused on developing locally ... Driving CRO and trial sites with study startup activities, including IRB/IEC submissions 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 Jun 14, 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 Clinical Study Startup, and why are they important?

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
Senior Clinical Study Manager

Senior Clinical Study Manager

Integrated Resources INC

Woodcliff Lake, NJ

Full-time

Posted 21 hours ago

Job description

Job Description

JOB DESCRIPTION:

  • Provide operational leadership for assigned trials executing them on time and within budget
  • Overall coordination and management of clinical trials from startup to closeout
  • Liaise with other functional areas to identify issues, evaluate and make sound business decisions and ensure implementation of timely solutions.
  • Identify and select high-quality clinical vendors in conjunction with the appropriate team members
  • Work with the contracting/ budgeting team to ensure that vendor responsibilities and payment terms are clearly defined.
  • Manage and effectively provide oversight of assigned clinical vendors and functional service providers to ensure data integrity and adherence with regulatory requirements.
  • Assure that team is receiving high quality, on time deliverables from internal and external vendors.
  • Collaborate with other team members to coordinate the development and finalization of key study documents including protocols, case reports forms, informed consent documents, study management plans and final clinical study reports.
  • Work with finance manager on financial aspects of the project(s), including milestone payments, and monthly pass through invoices
  • Lead or facilitate teleconferences with internal or external group.
  • Oversee Clinical Trial Coordinator for assigned project to ensure successful management of project(s), including development of the project plan, maintenance of trackers, and generation of metrics reports
  • Assume co-monitoring responsibilities as needed.
  • Communicate with Principle Investigator, Study Co-Coordinator, and/ CRO (if applicable) to proactively recognize problem situations and work with other team members as required to resolve issues
  • Manage the publication process in conjunction with the publications team to assure that submission timelines are met.
  • Monitor and report clinical trial status using standard and adhoc review & reporting procedures and identify issues that affect functions. Ensure that each function is accountable for their deliverables.
  • In collaboration with Project Management and utilizing various tracking mechanisms, manage clinical trial project milestones and budget. Proactively identify issues and escalate to appropriate managers.

REQUIREMENTS:

  • At least 10 years of experience in the management of clinical trials, significant knowledge of overall clinical drug development and general clinical research operations in Big Pharma.
  • Ability to manage multiple projects simultaneously with strong organizational and planning skills.
  • Well-developed analytical and problem solving skills. Communicates issues to Director with action plans for resolution.
  • Knowledgeable in all required regulatory and compliance standards and guidelines including ICH-GCP.
  • Ability to effectively work with teams and promote collaborations. Exceptional interpersonal skills including the ability to influence negotiate and resolve conflicts.
  • Excellent verbal and written communication skills and the ability to interact with all levels of management within the organization and to external business contacts. Experience using the Inform database, PowerPoint and Excel software.
  • Independent judgment and decision making skills with respect to functional responsibilities. Innovative and motivated in optimizing clinical operations processes to meet deliverables.
  • Minimum BS or BA in related field; focusing on biological science or nursing preferred or equivalent. Advanced Degree preferred
Qualifications

10 years of experience in the management of clinical trials

Additional Information

All your information will be kept confidential according to EEO guidelines.

Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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