ZipRecruiter

Log In

2

Part Time Clinical Study Start Up Jobs (NOW HIRING)

CenExel

PRN - Clinical Research RN I

Hollywood, FL · On-site

CenExel is a leading nationwide clinical research site and patient network serving the life ... Regularly attends training meetings, staff meetings, initiation meetings, study start-up meetings ...

CenExel

PRN - Clinical Research RN I

Hollywood, FL · On-site

CenExel is a leading nationwide clinical research site and patient network serving the life ... Regularly attends training meetings, staff meetings, initiation meetings, study start-up meetings ...

Thermo Fisher Scientific

... end clinical trial support -- from study start-up through close-out -- across commercial and ... Permanent employment * Full-time (40 hours/week) or Part-time (32 hours/week) options available ...

next page

Showing results 1-20

People also search for

All JobsClinical Study Start Up JobsPart Time Clinical Study Start Up Jobs

Part Time Clinical Study Start Up information

See salary details

$22K

$125.3K

$206K

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

As of May 30, 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.
Part-Time Clinical Research gastroenterologist

Part-Time Clinical Research gastroenterologist

ProTouch Staffing

Asheville, NC

$100 - $250/hr

Part-time

Posted 27 days ago

Job description

Job Title:  Part-Time Clinical Research gastroenterologist

Compensation: $100 - $250 per hour
Schedule: Part-Time (0-8 hours)
start date: 0-6 months

About the Role

We are seeking a board-certified to serve as a Clinical Research gastroenterologist

You will oversee protocol compliance, ensure patient safety, and collaborate with sponsors, CROs, and cross-functional teams to drive the success of Phase I-IV clinical trials.

Key Responsibilities

  • Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for dermatology-focused and multi-therapeutic clinical trials.
  • Conduct medical screenings, dermatological assessments, and physical examinations for study participants.
  • Provide clinical oversight and medical care to study subjects in accordance with protocols, ICH-GCP, and regulatory requirements.
  • Collaborate with study coordinators, nurses, and research staff to ensure compliance and accurate documentation.
  • Document all patient interactions, adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.
  • Establish and maintain strong working relationships with sponsors, CROs, monitors, and IRBs.
  • Participate in site initiation visits (SIVs), monitoring visits, and audits.
  • Contribute to protocol feasibility reviews, study design input, and recruitment strategies.
  • Attend investigator meetings and provide medical expertise on dermatology-related endpoints and safety monitoring.
  • Stay current on clinical research regulations and advances in dermatology and investigational therapies.

Qualifications

  • M.D. or D.O. with an active, unrestricted NC medical license.
  • Board certification in required.
  • Valid DEA license and BLS/ACLS certification.
  • Prior experience in clinical research/clinical trials strongly preferred (training available for motivated candidates).
  • Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS).
  • Strong interpersonal and communication skills with the ability to work in a multidisciplinary, fast-paced environment.
  • Commitment to ethical research practices and patient-centered care.

Compensation & Benefits

  • Competitive hourly rate: $100 - $250 based on experience.
  • Flexible part-time schedule.
Protouch Staffing logo

About Protouch Staffing

Sourced by ZipRecruiter

Protouch Staffing, based in Plano, Texas, is a leading provider in the healthcare staffing industry. Established over 30 years ago, the company prides itself on delivering quality services in the fields of nursing, allied health, pharmaceuticals, healthcare IT, and more. Committed to building lasting relationships, Protouch Staffing continually exceeds client expectations by providing unparalleled service, superior patient care, and talented healthcare professionals.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Frisco, TX, US

Year founded

1989

View All Protouch Staffing Jobs

Apply