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Clinical Trials Part Time Jobs in Indiana (NOW HIRING)

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Clinical Trials Part Time information

What is a clinical trials part time job?

Clinical trials part time jobs are positions in which individuals assist with the planning, execution, or management of clinical research studies on a part-time basis. These roles may include research assistants, coordinators, data managers, or nurses, and offer flexible work hours to accommodate other commitments. Part-time staff are crucial in supporting the collection and management of data, participant recruitment, and ensuring compliance with study protocols. These positions are ideal for students, professionals seeking flexible hours, or those looking to gain experience in clinical research without committing to a full-time schedule.

What are the common responsibilities and challenges of working part-time in clinical trials?

Part-time roles in clinical trials typically involve supporting research coordinators, assisting with data collection and entry, participant recruitment, and ensuring compliance with study protocols. A common challenge can be balancing workload and communication with the team, as studies often require careful coordination and timely updates. Flexibility and strong organizational skills are important, as part-time staff may need to quickly adapt to changing priorities while maintaining high-quality standards. Despite these challenges, part-time positions offer valuable exposure to clinical research processes and can serve as a stepping stone to full-time roles or advanced positions in the field.

What are the key skills and qualifications needed to thrive in a part-time clinical trials role, and why are they important?

To thrive in a part-time clinical trials role, you typically need a background in life sciences or healthcare, attention to detail, and familiarity with clinical research protocols. Experience with electronic data capture (EDC) systems, knowledge of Good Clinical Practice (GCP), and sometimes certification such as SOCRA or ACRP are commonly required. Strong organizational skills, clear communication, and adaptability help you excel in coordinating studies and working with diverse teams. These skills ensure accurate data collection, regulatory compliance, and efficient support of clinical research objectives.

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

AspectClinical Trials Part TimeClinical Research Coordinator
CredentialsTypically requires a degree in health sciences or related field; certifications like CCRP are a plusRequires a degree in health sciences or related field; often holds certifications such as CCRP or CCRC
Work EnvironmentPart-time roles in clinics, hospitals, or research facilities; flexible schedulesFull-time or part-time roles in research sites, hospitals, or pharmaceutical companies
Employer & IndustryPharmaceutical companies, CROs, academic institutionsResearch sites, hospitals, pharmaceutical companies

Clinical Trials Part Time roles focus on supporting specific trial activities with flexible hours, while Clinical Research Coordinators oversee entire study processes, often working full-time. Both roles require similar credentials and are integral to clinical research, but differ mainly in scope and schedule.

What are the most commonly searched types of Clinical Trials jobs in Indiana?

The most popular types of Clinical Trials jobs in Indiana are:

Clinical Trials Part Time jobs near you
Infographic showing various Clinical Trials Part Time job openings in Indiana as of August 2026, with employment types broken down into 100% Part Time. Highlights an 67% In-person, and 33% Remote job distribution.

Internist - Clinical Research Investigator

Merrillville, IN

ECN Operating LLC
See more jobs at ECN Operating LLCexternal

Part-time, Per diem

Posted 2 days ago

New

Job description

Position Overview

Elite Clinical Network (ECN) is seeking a dedicated and research-oriented Internist - Clinical Research Investigator to join our expanding team of clinical professionals. The ideal candidate will play a critical role in the conduct of clinical trials by serving as a Principal Investigator (PI) or Sub-Investigator, while continuing to provide high-quality medical care to adult patients within a clinical research setting. This is a part time/per diem position with a unique opportunity to contribute to the advancement of medicine through clinical studies.

Key Responsibilities

  • Serve as Principal Investigator or Sub-Investigator on multiple Phase I–IV clinical trials.
  • Perform comprehensive physical exams and clinical assessments for protocol screening and enrollment.
  • Evaluate patient eligibility based on inclusion/exclusion criteria of clinical protocols.
  • Provide medical oversight for clinical trial participants, including safety assessments, adverse event evaluations, and ongoing care.
  • Collaborate closely with Clinical Research Coordinators, Sponsors, and Monitors to ensure protocol compliance and data integrity.
  • Review and sign off on source documents, case report forms (CRFs), and regulatory documentation.
  • Maintain detailed and accurate clinical trial documentation in compliance with ICH-GCP, FDA, and sponsor requirements.
  • Participate in Site Initiation Visits (SIVs), Monitoring Visits, and Audits as needed.
  • Manage chronic and acute conditions among study participants in alignment with standard care and protocol guidelines.
  • Educate and counsel patients on study procedures, informed consent, and potential side effects.
  • Support recruitment efforts and promote patient retention in trials.

Qualifications

  • MD or DO degree from an accredited medical school.
  • Valid, unrestricted medical license in the state of employment.
  • Board Certified or Board Eligible (BC/BE) in Internal Medicine.
  • BC/BE in Family Medicine or Geriatric Medicine will also be considered.
  • Current Good Clinical Practice (GCP) certification or willingness to obtain prior to start.
  • Minimum of 1 year of experience in clinical practice; prior clinical research experience preferred but not required.

Preferred Skills

  • Familiarity with FDA, ICH-GCP, and clinical trial protocols.
  • Experience managing or participating in industry-sponsored clinical trials.
  • Strong attention to detail and ability to document accurately.
  • Excellent interpersonal and communication skills for patient interaction and sponsor collaboration.
  • Ability to work collaboratively with a cross-functional team in a fast-paced research environment.
  • Comfortable using electronic medical records (EMRs) and clinical trial management systems (CTMS).
  • DEA license (preferred).