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Internship Clinical Study Startup Jobs in Virginia

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Leesburg, VA · On-site

... Internships and Residencies in the U.S. • WOOF University, offering abundant CE for Doctors and Staff. • Robust Clinical Studies program. • Opportunities to give back through strong Shelter ...

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Internship Clinical Study Startup information

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

The most popular types of Clinical Study Startup jobs in Virginia are:

Internship Clinical Study Startup jobs near you

(Senior) Clinical Study Manager, Clinical Development

Tempus

Triangle, VA

$100K - $140K/yr

Full-time

Posted 17 days ago

Job description

Passionate about precision medicine and advancing the healthcare industry?

Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.

We are seeking a highly motivated and detail-oriented Senior Clinical Study Manager (CSM) to join our Clinical Development team. In this role, you will lead the planning, execution, and management of both prospective and retrospective clinical evidence generation studies.

The ideal candidate thrives at the intersection of oncology, genomics, and data science. You will be responsible for ensuring that clinical studies are conducted with the highest quality standards, on time, and within budget, while leveraging Tempus's unique multimodal data platform.

Key Responsibilities

  • Study Leadership: Lead the end-to-end management of multiple clinical studies, including prospective observational trials and retrospective Real-World Evidence (RWE) studies.

  • Operational Planning: Develop study protocols, Informed Consent Forms (ICFs), Case Report Forms (CRFs), and study-specific manuals.

  • Vendor & Site Management: Oversee CROs, central labs, and clinical trial sites. Conduct site identification, feasibility assessments, and maintain strong relationships with Principal Investigators.

  • Data Integrity: Partner with Data Science and Bio-informatics teams to ensure high-quality data collection and clean datasets for retrospective analysis.

  • Compliance: Ensure all study activities adhere to ICH-GCP guidelines, HIPAA regulations, and internal Standard Operating Procedures (SOPs).

  • Cross-functional Collaboration: Work closely with Medical Affairs, Product, Legal, and Engineering teams to align study objectives with company milestones.

  • Timeline & Budget Tracking: Manage study milestones, identify potential risks to timelines, and implement mitigation strategies to keep projects on track.

Qualifications

  • Education: Bachelor's degree in a Life Sciences, Nursing, or related field (Advanced degree such as MS, MPH, or PhD preferred).

  • Experience: 5+ years of clinical trial management experience within a Biotech, Pharma, or CRO environment.

  • Domain Expertise: Strong understanding of oncology and/or molecular diagnostics. Experience with Real-World Data (RWD) or retrospective cohort studies is highly desirable.

  • Technical Skills: Proficiency with EDC systems, CTMS, and eTMF platforms. Familiarity with SQL or data visualization tools is a plus.

  • Soft Skills: Exceptional project management, communication, and problem-solving skills. Ability to work in a fast-paced, "startup" environment.

#LI-NK1

$100,000 - $140,000


The expected salary range may vary for other locations. Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.

We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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