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Part Time Clinical Study Start Up Jobs (NOW HIRING)

Syneoshealth

CRC II (Onsite) - Marietta, GA

Concord, NC

$22.50 - $30/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 ...

Icon plc

Clinical Study Coordinator

Washington, DC · On-site

Clinical Study Coordinator ICON is a global healthcare intelligence and clinical research ... Ensuring the users enter the right code and subject number on each study device prior to the start ...

CenExel

Clinical Research RN, PRN

Englewood, CO · On-site

$36 - $46/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 ...

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 ...

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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 Aug 3, 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 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 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 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 are the most commonly searched types of Clinical Study Start Up jobs? The most popular types of Clinical Study Start Up jobs are:
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 July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $125,290 per year, or $60.2 per hour.

Clinical Research Coordinator (Part-time)

Tandem Clinical Research

Somers Point, NJ • On-site

$24.75 - $32.75/hr

Part-time

Posted 4 days ago

Job description

Clinical Research Coordinator (CRC)
The Clinical Research Coordinator (CRC) is responsible for overseeing and managing the daily operational activities of assigned clinical research studies. This role works closely with investigators, clinical staff, study participants, sponsors, and CROs to ensure that all research activities are conducted in compliance with study protocols, regulatory requirements, and ethical standards.
The CRC serves as the primary owner of study coordination, documentation, data management, and sponsor communication, supporting compliant trial execution from study start-up through close-out.
Key Responsibilities
Study Management & Coordination
  • Organize, plan, and coordinate all aspects of assigned clinical trials from initiation through close-out.
  • Support study start-up activities including feasibility, regulatory submissions, and site activation.
  • Attend investigator meetings, site initiation visits, and other study-related meetings.
  • Manage visit schedules and coordinate study-related activities across clinical teams.

Recruitment, Enrollment & Consent
  • Collaborate with recruitment teams to support participant screening and enrollment.
  • Conduct informed consent discussions with participants, ensuring understanding of study requirements and documentation of consent.
  • Ensure protocol and regulatory requirements are met throughout the enrollment process.

Clinical Oversight & Subject Monitoring
  • Monitor and assess study subjects in accordance with protocol requirements.
  • Identify, document, and report adverse events in collaboration with the Principal Investigator and clinical staff.
  • Escalate safety concerns and protocol issues to the PI, sponsor, and IRB as required.

Documentation, Data & Systems
  • Maintain accurate and complete source documentation, case report forms, regulatory files, and study records.
  • Enter study data into EDC and other required systems and manage study databases.
  • Complete, verify, and resolve case report forms and sponsor or monitor queries in a timely manner.
  • Report protocol deviations to the PI, sponsor, and IRB as required.

Investigational Product & Specimen Management
  • Manage investigational product accountability records and documentation.
  • Collect, process, package, and ship study specimens per protocol requirements.
  • Perform phlebotomy and handle biological specimens in accordance with study protocols and safety guidelines, when trained and authorized.

Quality, Compliance & Team Support
  • Ensure all study activities comply with SOPs, GCP, and regulatory requirements.
  • Support quality assurance activities and audit readiness.
  • Provide assistance and mentorship to fellow coordinators as needed.
  • Maintain strict confidentiality of participant and study information.

Communication & Outreach
  • Serve as the primary point of contact for sponsor and CRO communications.
  • Participate in occasional outreach or community events related to clinical trials.
  • Ensure timely, accurate communication of study updates and issues.

Additional Responsibilities
This job description outlines the primary responsibilities of the Clinical Research Coordinator but is not exhaustive. Additional duties may be assigned as needed to support study requirements, operational needs, and organizational priorities. Responsibilities may evolve based on protocol complexity and business needs.
Requirements
  • Knowledge, Skills, and Abilities
  • Strong leadership and communication skills
  • Exceptional organizational and multitasking abilities
  • High attention to detail and commitment to regulatory compliance
  • Ability to work independently and collaboratively in a multidisciplinary environment
  • Strong time management and operational efficiency skills
  • Proficiency with office equipment and study-specific systems
  • Ability to maintain strict confidentiality
  • Required Experience & Qualifications
  • Education: Bachelor's degree in a related field
  • Experience: Minimum of two (2) years of clinical research or clinical trial management experience
  • Preferred Credentials: Medical certification or licensure (e.g., MS, LPN, RN)
  • Phlebotomy: Prior experience performing blood draws and handling biological specimens required

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