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How much do part time international clinical research jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for part time international clinical research in the United States is $22.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.

What is a part time international clinical research?

A part-time international clinical research position involves supporting or conducting medical research studies that take place across different countries, but on a part-time basis. These roles may include coordinating clinical trials, collecting and managing data, ensuring regulatory compliance, and collaborating with global teams. Professionals in this field help advance medical knowledge and treatments while working flexible hours. The work often requires strong communication skills, attention to detail, and familiarity with international regulations and protocols.

What are the key skills and qualifications needed to thrive as a part time international clinical research professional?

To thrive as a Part Time International Clinical Research professional, you need a background in life sciences, knowledge of clinical trial protocols, and familiarity with international research regulations, typically supported by a relevant degree. Experience with data management systems, regulatory submission software, and certifications such as Good Clinical Practice (GCP) are often required. Strong organizational skills, cross-cultural communication, and adaptability help you effectively manage global projects and collaborate with international teams. These competencies are crucial for ensuring compliance, data integrity, and the successful execution of clinical trials across diverse regions.

What are some common challenges faced by part time international clinical research professionals, and how can they be addressed?

Part-time international clinical research professionals often face challenges related to time zone differences, coordinating with global teams, and managing study documentation across multiple regulatory frameworks. Effective communication and strong organizational skills are essential for navigating these complexities. Utilizing digital collaboration tools and maintaining clear documentation can help ensure smooth project progress and compliance with international standards.

What is the difference between Part Time International Clinical Research vs Part Time Clinical Research Coordinator?

AspectPart Time International Clinical ResearchPart Time Clinical Research Coordinator
CredentialsOften requires clinical research certifications, bilingual skills, and understanding of international regulationsTypically requires research certifications and experience in clinical trial coordination
Work EnvironmentGlobal, often remote or in international sites, with cross-cultural interactionsPrimarily in local clinics or research sites, focused on trial management
Employer & Industry UsagePharmaceutical companies, CROs, and international research organizationsHospitals, research institutions, and local clinics
Search & Comparison IntentUnderstanding international aspects of clinical research rolesFocus on local trial coordination and management

Part Time International Clinical Research involves working on global trials, often requiring international regulations knowledge and bilingual skills. In contrast, Part Time Clinical Research Coordinator focuses on managing local clinical trials within specific sites. Both roles require research certifications but differ mainly in scope and work environment.

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What cities are hiring for Part Time International Clinical Research jobs?

Cities with the most Part Time International Clinical Research job openings:

What are the most commonly searched types of International Clinical Research jobs?

The most popular types of International Clinical Research jobs are:

What job categories do people searching Part Time International Clinical Research jobs look for?

The top searched job categories for Part Time International Clinical Research jobs are:

Part Time International Clinical Research jobs near you
Infographic showing various Part Time International Clinical Research job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $47,241 per year, or $22.7 per hour.

Clinical Research Coordinator (Part-time)

Prolerity Clinical Research

Somers Point, NJ • On-site

$24.75 - $32.75/hr

Part-time

Posted 20 days ago

Job description

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