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Internship Clinical Study Start Up Jobs (NOW HIRING)

CEDENT

Study Start-Up Manager

Wilmington, DE · On-site

Summary We are looking for a Study Start-Up Manager with extensive experience to lead clinical study start-up activities. This role requires a strong background in regulatory processes, site ...

Tempus

Study Start-Up Manager

Chicago, IL · On-site

$80K - $100K/yr

Tempus created the TIME clinical trials network to increase patient access to clinical trials by ... We are looking for an experienced Study Start-Up Manager who will work with our cross- functional ...

CYNET SYSTEMS

Study Start-Up Lead

South San Francisco, CA · On-site

$70 - $75/hr

Enable innovative clinical trial delivery and address study start-up needs across various ... therapeutic areas. * Collaborate with local internal and external country teams, global study teams ...

Tempus

Study Start-Up Manager

Chicago, IL · On-site

$80K - $100K/yr

Tempus created the TIME clinical trials network to increase patient access to clinical trials by ... We are looking for an experienced Study Start-Up Manager who will work with our cross- functional ...

Glaukos

Manager Study Start-up

San Clemente, CA

Clinical Study Manager The Clinical Study Manager is responsible for the end-to-end management and ... Lead the operational execution of clinical studies from start-up through close-out, including site ...

Glaukos

Manager Study Start-up

San Clemente, CA

Clinical Study Manager The Clinical Study Manager is responsible for the end-to-end management and ... Lead the operational execution of clinical studies from start-up through close-out, including site ...

Glaukos

Manager Study Start-up

San Clemente, CA · On-site

Clinical Study Manager The Clinical Study Manager is responsible for the end-to-end management and ... What You'll Do: • Lead the operational execution of clinical studies from start-up through close ...

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Internship Clinical Study Start Up information

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How much do internship clinical study start up jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for internship clinical study start up in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What is an internship in clinical study start up?

An Internship in Clinical Study Start Up is a temporary position where students or recent graduates assist with the initial phases of clinical trials. This role typically involves helping with regulatory document preparation, site selection, ethics committee submissions, and coordination between study teams. Interns gain hands-on experience in clinical research processes, compliance requirements, and project management. It’s a valuable opportunity for those interested in pharmaceutical, biotechnology, or healthcare research careers.

What types of projects and tasks can an intern expect to handle in clinical study start up?

As an intern in Clinical Study Start Up, you will typically support activities such as preparing regulatory submission documents, tracking site activation milestones, and assisting with communication between study sites and sponsors. You'll gain hands-on experience with study documentation, database entry, and compliance checks, often working closely with clinical operations teams and regulatory specialists. This role offers valuable insight into the clinical trial initiation process and provides a strong foundation for future roles in clinical research.

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

To thrive as an Internship Clinical Study Start Up, you need foundational knowledge of clinical research processes, regulatory requirements, and attention to detail, often gained through coursework in life sciences or related fields. Familiarity with clinical trial management systems (CTMS), Microsoft Office Suite, and understanding of ICH-GCP guidelines are typically important. Strong organizational, communication, and teamwork skills help you coordinate study start-up activities and collaborate with diverse stakeholders. These competencies ensure efficient study initiation, regulatory compliance, and effective cross-functional collaboration in clinical research environments.

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

AspectInternship Clinical Study Start UpClinical Research Coordinator
CredentialsTypically pursuing or holding a relevant degree (e.g., life sciences, healthcare)Often requires a degree in health sciences or related field, with certifications preferred
Work EnvironmentAssists in preparing sites for clinical trials, often in a training or entry-level capacityManages daily trial activities at clinical sites, coordinating with investigators and staff
Employer & Industry UsageUsed in pharmaceutical companies, CROs, and research institutions during early trial phasesCommonly employed in hospitals, research centers, and clinical trial sites

While both roles support clinical trials, an Internship Clinical Study Start Up focuses on assisting with trial preparations and site readiness, often as an entry-level position or trainee. In contrast, a Clinical Research Coordinator manages ongoing trial activities, ensuring compliance and data integrity at clinical sites.

What cities are hiring for Internship Clinical Study Start Up jobs?

Cities with the most Internship Clinical Study Start Up job openings:

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

The most popular types of Clinical Study Start Up jobs are:

What states have the most Internship Clinical Study Start Up jobs?

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

Internship Clinical Study Start Up jobs near you

Study Start-Up Manager

CEDENT

Wilmington, DE • On-site

Full-time

Re-posted 26 days ago

Job description

Summary

We are looking for a Study Start-Up Manager with extensive experience to lead clinical study start-up activities. This role requires a strong background in regulatory processes, site management, and expertise in ensuring compliance with local and international guidelines, particularly ICH-GCP.
 

Key Responsibilities
  • Lead and manage start-up activities for clinical studies, ensuring compliance with local and international guidelines (ICH-GCP).
  • Prepare, review, and track site regulatory documentation throughout the study start-up phase.
  • Collaborate with Clinical Research Associates (CRAs) and the local study team to meet start-up milestones.
  • Participate in Local Study Team meetings and report on site performance metrics.
  • Ensure the timely submission of documents to regulatory authorities and maintain the trial master file (eTMF).

Qualifications
  • Minimum 3 years of experience in Clinical Study Start-Up (full-time).
  • At least 1 year of hands-on experience with Veeva Vault.
  • Strong background in informed consent review and negotiation.
  • Bachelor’s degree (higher degree preferred) with knowledge of clinical trial processes (Phases II-IV) and ICH-GCP.
  • Excellent communication, organizational, and project management skills.
  • Strong problem-solving and negotiation abilities.
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About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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