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Full Time Clinical Study Startup Jobs (NOW HIRING)

ICON

Global Study Manager

In this role, you will lead global clinical trials from sourcing strategy and RFP development ... Accountable for the development of realistic detailed study startup and/or study management ...

Icon plc

In this role, you will lead global clinical trials from sourcing strategy and RFP development ... Accountable for the development of realistic detailed study startup and/or study management ...

RadNet

Senior Clinical Studies Associate

Somerville, MA · On-site

$71K/yr

Support study startup, maintenance and closeout activities. * Identify and escalate routine study issues, risks, or delays as appropriate. Clinical Documentation & Compliance * Draft, update, and ...

RadNet

Senior Clinical Studies Associate

Somerville, MA

$71K - $96K/yr

Support study startup, maintenance and closeout activities. * Identify and escalate routine study issues, risks, or delays as appropriate. Clinical Documentation & Compliance * Draft, update, and ...

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Nutrafol

Sr. Clinical Research Manager

$150K - $165K/yr

About You Nutrafol is seeking a full-time Clinical Research Manager to join our team. This person ... Lead full study lifecycle execution from startup through closeout. * Prepare and manage IRB ...

Evolution Research Group

Study Manager

Miami, FL · On-site

$85K - $95K/yr

Lead site clinical team in sponsor study startup and study conduct. * Ensure effective study plans are in place and operational for each trial and work proactively with the Clinical Trial Team to set ...

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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 ...

CenExel

Study Startup Specialist I

Savannah, GA · On-site

CenExel is a leading nationwide clinical research site and patient network serving the life ... full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD ...

Pathos

Director, Clinical Science

New York, NY · On-site

$200K - $240K/yr

You own protocol development, data review, clinical document authorship, and site-level scientific support from study startup through closeout. You will work closely with Clinical Operations ...

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All JobsFull Time Clinical Study Startup Jobs

Full Time Clinical Study Startup information

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How much do full time clinical study startup jobs pay per hour?

As of Jul 2, 2026, the average hourly pay for full time clinical study startup in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What is a Full Time Clinical Study Startup role?

A Full Time Clinical Study Startup role involves overseeing and coordinating the initial phases of clinical trials, such as site selection, regulatory document collection, ethics submissions, and study initiation activities. Professionals in this position ensure that all necessary approvals and documentation are in place to begin the clinical study on schedule. They work closely with clinical research teams, investigators, and regulatory bodies to manage timelines and compliance with applicable guidelines. This role is crucial for ensuring that clinical trials start efficiently and adhere to all regulatory requirements.

What are the key skills and qualifications needed to thrive as a Full Time Clinical Study Startup professional, and why are they important?

To thrive as a Full Time Clinical Study Startup professional, you need a strong background in clinical research, regulatory requirements, and project management, often supported by a life sciences degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), regulatory documentation platforms, and Good Clinical Practice (GCP) certification is typically required. Exceptional organizational skills, attention to detail, and effective communication are vital soft skills for coordinating stakeholders and ensuring study timelines are met. These competencies are essential for ensuring the compliant, efficient, and timely initiation of clinical studies.

What are some common challenges faced during the clinical study startup phase, and how can they be addressed?

One common challenge in clinical study startup roles is coordinating timelines between multiple stakeholders, such as regulatory bodies, ethics committees, and site staff. Delays often occur due to incomplete documentation or differing site requirements. Effective communication, proactive planning, and familiarity with regulatory processes are key to overcoming these obstacles. Working closely with cross-functional teams and maintaining detailed trackers can help ensure a smoother and faster study initiation.
More about Full Time Clinical Study Startup jobs
What cities are hiring for Full Time Clinical Study Startup jobs? Cities with the most Full Time 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:
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What job categories do people searching Full Time Clinical Study Startup jobs look for? The top searched job categories for Full Time Clinical Study Startup jobs are:
Full Time Clinical Study Startup jobs near you
Infographic showing various Full Time Clinical Study Startup job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 97% Full Time, and 2% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Study Recruiter

Vivo Clinical Testing

Austin, TX • On-site

$14/hr

Full-time

Medical, PTO

Posted 7 days ago

Job description

Company Description
Vivo Clinical Testing Labs is an emerging clinical testing laboratory that opened in January 2017. It is located in North Austin, Texas. The lab specializes in the testing of topical antiseptics and personal care cosmetics.
Job Description
About the Position:
The Clinical Study Recruiter is responsible for finding, screening, and documenting participants for clinical trials conducted by Vivo Clinical Testing. Clinical Study Recruiters play a critical role in enabling clinical trials by building a database of willing and qualified study volunteers.
Major Duties:
Find clinical study volunteers to participate in testing.
Screen clinical study volunteers.
Maintain a database of clinical study volunteers.
Develop outreach efforts related to volunteer recruitment.
Interact directly with customers and study volunteers via phone, email and in person.
Interview prospective study subjects.
Coordinate with laboratory's Pricinipal Investigator to ensure adequate subject recruitment has been met for each study.
Maintain and improve study documentation and volunteer records such as consent forms.
Assist with sales, marketing, and outreach efforts as needed.
Interact with and provide detailed and accurate information to Accounting personnel.
Maintain a safe, fast-paced, and positive laboratory environment.
Assist with all the other aspects of a startup clinical lab, ranging from assembling office furniture to occasional Wal-Mart runs for office supplies.
Qualifications
Required Qualifications:
Good project management and time management skills.
Ability to be a self-starter and work cooperatively with others in a small-company environment.
Ability to treat at clinical study participants with respect and courtesy.
Skill and familiarity with social media.
Willingness to speak with members of the public to sign them up for testing.
Good work ethic.
Reliable transportation and safe driving history.
Desired Qualifications:
Prior experience working as a recruiter for a clinical testing lab.
Previous experience with outbound sales.
Strong project management skills.
Knowledge of, and experience with FDA Good Clinical Practice (GCP) regulations.
Experience managing and tracking outreach efforts (letters, ad campaigns, phone calls, etc.).
Strong knowledge of community outreach.
Proficiency in LibreOffice, especially Calc.
Proficiency in medical scheduling software, such as Clinical Conductor.
Additional Information
Compensation and Benefits:
- Pay for entry-level Clinical Study Recruiters is $14/hr. Other candidates' compensation commensurate with experience and skills.
- 2 weeks paid vacation
- Health insurance is NOT offered at this time.

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