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Study Start-Up Manager

Wilmington, DE

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 ...

AstraZeneca

Study Start Up Manager

Wilmington, DE · Hybrid

Accountabilities: - Obtain and maintain essential documentation in compliance with ICH-GCP, AZ Procedural Documents. - Assist in coordination and administration of clinical studies from start-up ...

AstraZeneca

Study Start Up Manager

Wilmington, DE · On-site

Accountabilities: - Obtain and maintain essential documentation in compliance with ICH-GCP, AZ Procedural Documents. - Assist in coordination and administration of clinical studies from start-up ...

AstraZeneca

Study Start Up Manager

Wilmington, DE · Hybrid

Accountabilities: - Obtain and maintain essential documentation in compliance with ICH-GCP, AZ Procedural Documents. - Assist in coordination and administration of clinical studies from start-up ...

AstraZeneca

Study Start Up Manager

Wilmington, DE · On-site

Accountabilities: - Obtain and maintain essential documentation in compliance with ICH-GCP, AZ Procedural Documents. - Assist in coordination and administration of clinical studies from start-up ...

Novartis

Study Start Up Manager

Milano, TX · On-site

Global Clinical Operations (GCO) is the powerhouse behind Novartis clinical trials, redesigned to accelerate study start-up, enhance trial delivery, and ensure patients gain timely access to ...

Icon plc

Manager of Study Start Up

Blue Bell, PA

Manager of Study Start Up ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and ...

ICON

Manager of Study Start Up

Blue Bell, PA · On-site +1

Manager of Study Start Up ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and ...

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How much do clinical study start up jobs pay per year?

As of May 29, 2026, the average yearly pay for clinical study start up in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.

What is a Clinical Study Start Up job?

A Clinical Study Start Up job focuses on the early stages of a clinical trial, ensuring all regulatory, ethical, and logistical requirements are met before patient enrollment begins. Responsibilities typically include preparing and submitting regulatory documents, obtaining ethics committee approvals, negotiating site contracts, and ensuring site readiness. This role requires strong knowledge of clinical trial regulations, attention to detail, and collaboration with cross-functional teams. Effective study start-up is critical for timely trial initiation and overall study success.

What are the key skills and qualifications needed to thrive in the Clinical Study Start Up position, and why are they important?

To thrive in a Clinical Study Start Up role, you need a solid understanding of clinical research processes, regulatory guidelines, and project management, often supported by a degree in life sciences or a related field. Familiarity with tools like CTMS (Clinical Trial Management Systems), IRB/ethics submission platforms, and knowledge of GCP (Good Clinical Practice) certifications are commonly required. Strong organizational skills, attention to detail, effective communication, and the ability to juggle multiple tasks help candidates excel in this position. These skills are crucial for ensuring timely study initiation, regulatory compliance, and seamless collaboration among clinical teams, sites, and sponsors.

What are the typical challenges faced in a Clinical Study Start Up position?

One common challenge in a Clinical Study Start Up role is managing tight timelines and coordinating across various stakeholders, such as clinical sites, ethics committees, and sponsors, to ensure all regulatory and operational requirements are met before study launch. You may also need to navigate complex documentation, regulatory submissions, and evolving compliance standards, all while maintaining clear communication and attention to detail. Adapting quickly to changes and proactively solving issues as they arise will help you succeed in this fast-paced environment. Many professionals find the work both stimulating and rewarding, as it plays a crucial role in the successful launch of new clinical studies.
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Clinical Study Start Up jobs near you
Infographic showing various Clinical Study Start Up job openings in the United States as of May 2026, with employment types broken down into 9% As Needed, 59% Full Time, 9% Part Time, and 23% Contract. Highlights an 93% Physical, and 7% Remote job distribution, with an average salary of $125,290 per year, or $60.2 per hour.
Clinical Study Start Up Lead

Clinical Study Start Up Lead

Dawar Consulting, Inc.

South San Francisco, CA

$80 - $90/hr

Full-time

Posted 24 days ago

Job description

Our client, a world leader in diagnostics and biotechnology, is looking for a "Clinical Study Start Up Lead” based out of South San Francisco, CA.


Job Duration: Long Term Contract (Possibility Of Extension)

Pay Rate : $90/hr on W2


We are seeking a Clinical Study Start-Up professional to drive the efficient and compliant initiation of clinical trials. This role leads country-level start-up strategy, regulatory submissions, and site activation while ensuring alignment with global timelines and standards. You will collaborate with cross-functional teams, CROs, and regulatory bodies to enable seamless clinical trial execution.


Key Responsibilities:

  • Lead country start-up strategy and execution for clinical trials
  • Oversee site activation, regulatory submissions, and amendments
  • Ensure compliance with ICH-GCP, EU CTR, and local regulations
  • Manage ICF processes, site documentation, and trial materials
  • Coordinate with CROs, investigators, and regulatory authorities
  • Drive process improvements, automation, and standardization
  • Manage budgets, contracts, and payment oversight
  • Support cross-functional alignment with global and regional teams


Qualifications:

  • Degree in Life Sciences (Bachelor’s required; advanced degree preferred)
  • 2–6+ years of experience in clinical trial start-up / clinical operations
  • Strong knowledge of regulatory submissions and study start-up processes
  • Experience with clinical systems (Veeva Vault, CTIS, RIM, etc.)
  • Experience working with CROs and external vendors


Key Skills:

  • Strong communication, stakeholder management, and collaboration
  • Excellent organizational, analytical, and problem-solving skills
  • Ability to manage multiple priorities in a global, matrixed environment
  • Detail-oriented with a focus on compliance and timelines



If interested, please send us your updated resume at

hr@dawarconsulting.com/akansha@dawarconsulting.com