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Clinical Study Start Up Associate Jobs (NOW HIRING)

CEDENT

Study Start-Up Manager

Wilmington, DE · On-site

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 ...

Emmes

Study Start-Up Associate II

Rockville, MD · On-site +1

$34.25 - $46.75/hr

Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all ... Emmes Group is transforming the future of clinical research, bringing the promise of new medical ...

Emmes Group

Study Start-Up Associate II

Rockville, MD · On-site

$34.25 - $46.75/hr

Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all ... Emmes Group is transforming the future of clinical research, bringing the promise of new medical ...

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Study Start Up Associate II

Philadelphia, PA · On-site

$33.75 - $46.25/hr

Study Start-Up Specialist (Sponsor Dedicated) ICON is a global healthcare intelligence and clinical ... Your profile * BS/BA degree or Associates degree with 2 years of experience in clinical trial ...

Allucent

$11.50 - $15.50/hr

The Start Up Associate (Contractor) will support communication to RA/ IEC/ IRB as well as investigators and sites through the initial phase of a clinical study until the Site Initiation Visit. In ...

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Study Start Up Associate II

Cary, NC · On-site

$31 - $42.50/hr

Study Start-Up Specialist (Sponsor Dedicated) ICON is a global healthcare intelligence and clinical ... Your profile * BS/BA degree or Associates degree with 2 years of experience in clinical trial ...

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Study Start Up Associate II

Pittsburgh, PA · On-site

$32.50 - $44.50/hr

Study Start-Up Specialist (Sponsor Dedicated) ICON is a global healthcare intelligence and clinical ... Your profile * BS/BA degree or Associates degree with 2 years of experience in clinical trial ...

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Study Start Up Associate II

North Wales, PA · On-site

$32.50 - $44.25/hr

Study Start-Up Specialist (Sponsor Dedicated) ICON is a global healthcare intelligence and clinical ... Your profile * BS/BA degree or Associates degree with 2 years of experience in clinical trial ...

AstraZeneca

Study Start Up Manager

Wilmington, DE · On-site

Working across clinical operations, sites, and strategy, you will remove obstacles, compress ... Partner closely with CRAs and the Local Study Team/Local Study Associate Director to achieve start ...

AstraZeneca

Study Start Up Manager

Wilmington, DE · On-site

Working across clinical operations, sites, and strategy, you will remove obstacles, compress ... Partner closely with CRAs and the Local Study Team/Local Study Associate Director to achieve start ...

AstraZeneca

Study Start Up Manager

Wilmington, DE · On-site

Working across clinical operations, sites, and strategy, you will remove obstacles, compress ... Partner closely with CRAs and the Local Study Team/Local Study Associate Director to achieve start ...

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Clinical Study Start Up Associate information

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

As of Sep 10, 2026, the average hourly pay for clinical study start up associate in the United States is $31.54, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $41.59 per hour, depending on experience, location, and employer.

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Study Start-Up Manager

Wilmington, DE • On-site

CEDENT
IT Services • 11 - 50 employees
Learn more about CEDENTexternal

Full-time

Re-posted 15 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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