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Part Time Clinical Study Start Up Jobs (NOW HIRING)

Propedix, Inc.

Clinical Study Coordinator

Milford, MA

$25 - $30/hr

Clinical Study Coordinator (Consultant) About the Company: Propedix is a biopharma and consumer ... Study Start-Up & Regulatory Support and contribute to protocol development, study materials, and ...

Propedix, Inc.

Clinical Study Coordinator

Milford, MA

$25 - $30/hr

Study Start-Up & Regulatory • Support and contribute to protocol development, study materials, and operational plans • Coordinate IRB submissions, approvals, amendments, and site activation ...

Propedix, Inc.

Clinical Study Coordinator

Milford, MA

$25 - $30/hr

Study Start-Up & Regulatory • Support and contribute to protocol development, study materials, and operational plans • Coordinate IRB submissions, approvals, amendments, and site activation ...

Syneoshealth

OR

$24.25 - $32.25/hr

... for the study. * Participate in creation and review of timelines and start-up meetings ... Clinical Conduct * Perform all study activities following Good Clinical Practices (GCP). * Manage ...

Syneoshealth

OR

$24.25 - $32.25/hr

... for the study. - Participate in creation and review of timelines and start-up meetings ... Clinical Conduct - Perform all study activities following Good Clinical Practices (GCP). - Manage ...

Syneos Health

CRC II (Onsite) - Marietta, GA

Marietta, GA · On-site

$23 - $30.50/hr

... for the study. * Participate in creation and review of timelines and start-up meetings ... Clinical Conduct * Perform all study activities following Good Clinical Practices (GCP). * Manage ...

Syneos Health

CRC II (Onsite) - Memphis, TN

Memphis, TN · On-site

$23.50 - $31.25/hr

... for the study. * Participate in creation and review of timelines and start-up meetings ... Clinical Conduct * Perform all study activities following Good Clinical Practices (GCP). * Manage ...

Syneoshealth

OR

$24.25 - $32.25/hr

... for the study. * Participate in creation and review of timelines and start-up meetings ... Clinical Conduct * Perform all study activities following Good Clinical Practices (GCP). * Manage ...

CenExel

Clinical Research RN I, PRN

Marlton, NJ · On-site

$38 - $42/hr

Regularly attends training meetings, staff meetings, initiation meetings, study start-up meetings ... Ensures accountability and adequate supply for study and clinical drugs. * Assumes other duties and ...

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Part Time Clinical Study Start Up information

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$22K

$125.3K

$206K

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

As of May 29, 2026, the average yearly pay for part time 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 are the key skills and qualifications needed to thrive as a Part Time Clinical Study Start Up professional, and why are they important?

To thrive as a Part Time Clinical Study Start Up professional, you need knowledge of clinical research processes, regulatory requirements, and document management, often supported by a degree in life sciences or a related field. Experience with clinical trial management systems (CTMS), electronic trial master files (eTMF), and familiarity with ICH-GCP guidelines are typically required. Strong organizational skills, attention to detail, and effective communication are important soft skills for coordinating study documentation and stakeholder interactions. These skills ensure timely and compliant study initiation, which is crucial for the overall success of clinical trials.

What are some common challenges faced by professionals in a Part Time Clinical Study Start Up role, and how can they be managed?

Professionals in a Part Time Clinical Study Start Up role often encounter challenges related to tight timelines, coordinating with multiple stakeholders, and managing regulatory documentation. Balancing these demands on a part-time schedule requires strong organizational skills and proactive communication. Leveraging digital project management tools and maintaining regular updates with clinical operations and regulatory teams can help ensure smooth study activation. Staying informed about evolving regulatory requirements and fostering collaborative relationships within the team are also key to overcoming common hurdles in this role.

What is a Part Time Clinical Study Start Up role?

A Part Time Clinical Study Start Up professional assists with the initial phases of clinical trials, often on a part-time basis. Their responsibilities typically include preparing regulatory and ethics submissions, coordinating site activation activities, and managing documentation and timelines required to start a new clinical study. This role is vital in ensuring all pre-trial requirements are completed accurately and efficiently, enabling the study to begin on schedule. Part-time positions offer flexibility and may involve remote work or supporting multiple studies simultaneously.

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

AspectPart Time Clinical Study Start UpPart Time Clinical Research Coordinator
CredentialsTypically requires a degree in health sciences or related field; certifications like CCRP are a plusRequires similar health sciences background; often holds certifications like CCRP or CRC
Work EnvironmentPrimarily involved in planning, regulatory submissions, and site readinessFocuses on participant recruitment, data collection, and site management
Employer & Industry UsageUsed by sponsors, CROs, and research sites during study startup phaseCommonly employed at research sites and hospitals for ongoing study management

Part Time Clinical Study Start Up focuses on preparing and initiating clinical trials, including regulatory and site readiness tasks. In contrast, Part Time Clinical Research Coordinator handles participant interactions, data collection, and day-to-day study operations. Both roles require health sciences backgrounds and certifications, but their responsibilities differ significantly in the study lifecycle.

More about Part Time Clinical Study Start Up jobs
What cities are hiring for Part Time Clinical Study Start Up jobs? Cities with the most Part Time 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 Part Time Clinical Study Start Up jobs? States with the most job openings for Part Time Clinical Study Start Up jobs include:
What job categories do people searching Part Time Clinical Study Start Up jobs look for? The top searched job categories for Part Time Clinical Study Start Up jobs are:
Part Time Clinical Study Start Up jobs near you
Infographic showing various Part Time Clinical Study Start Up job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 70% Full Time, 28% Part Time, and 1% Nights. Highlights an 97% Physical, and 3% Remote job distribution, with an average salary of $125,290 per year, or $60.2 per hour.
Clinical Trial Assistant (Part-time)

Clinical Trial Assistant (Part-time)

Lumicell

Waltham, MA • On-site

Part-time, Contractor

Posted 14 days ago

Job description

At Lumicell, we'll give you the opportunity to harness all that's within you by working in a mission-driven start-up environment with high-performing employees, tackling some of the most important challenges in cancer surgery. We are working to revolutionize the way cancer surgery is performed today, starting with breast cancer. Women in the US have a 1 in 8 lifetime risk of being diagnosed with breast cancer. You will be a part of something groundbreaking as we expand our commercial launch and continue investigations in other cancer indications.
The Part-Time Clinical Trial Assistant (CTA) provides administrative and operational support to Lumicell's Clinical Affairs organization. This role supports regulated clinical documentation, clinical systems administration, and cross-functional coordination across Clinical Affairs, Clinical Operations, Regulatory Affairs, Quality Assurance and Medical Affairs. We are looking for a self-starting and collaborative team member to support multiple aspects of a post-market and investigational drug/device combination product.
What you will do:
Clinical Team Administration & Coordination
  • Prepare, distribute, and archive Clinical Team meeting agendas and minutes
  • Maintain and manage a Clinical Team action item tracker
  • Provide operational support across Clinical Affairs, Regulatory Affairs, and Medical Affairs
  • Support site engagement communications, including study start-up and follow-up support
  • Update and maintain Lumicell documents including Clinical Affairs SOPs, study procedures, templates, work instructions, etc.
  • Clinical Systems & Study Support
  • Perform Clinical Trial Management Software (CTMS) administrative tasks including study maintenance and data quality checks
  • Perform electronic Trial Master File (eTMF) administrative activities including filing, QC, and readiness support
  • Ensure documentation compliance with internal procedures and regulations
  • Maintains structure and organization for shared inboxes
  • Support data reconciliation activities

What you will bring:
  • Bachelor's degree or equivalent experience
  • 1-3+ years experience as a Clinical Trial Assistant or similar role
  • Experience with CTMS and eTMF systems
  • Familiarity with GCP, CFR, ICH and clinical operations best practices
  • Strong attention to detail and organizational skills

Position Type/Expected Hours of Work:
This is a part-time contract position, 20-25 hours per week.
Lumicell is committed to a diverse and inclusive workplace. We strive to recruit candidates who will bring inclusive mindsets and contribute to our values.
Lumicell is an Equal Opportunity Employer and does not discriminate based on race, national origin, gender, gender identity, sexual orientation, protected veteran status, disability, age, or other legally protected status. Lumicell will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

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