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Part Time Merck Clinical Trials information

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How much do part time merck clinical trials jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for part time merck clinical trials in the United States is $43.09, according to ZipRecruiter salary data. Most workers in this role earn between $36.54 and $43.03 per hour, depending on experience, location, and employer.

What is a part time Merck clinical trials job?

Part Time Merck Clinical Trials jobs typically involve supporting clinical research studies for Merck on a part-time basis. These roles may include assisting with data collection, patient recruitment, trial monitoring, and regulatory documentation. Employees in these positions usually work flexible hours and collaborate with research teams to ensure trials are conducted ethically and efficiently. Such jobs are suited for individuals with backgrounds in healthcare, science, or clinical research who are seeking flexible work opportunities.

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

To thrive in a Part Time Merck Clinical Trials role, you generally need a background in life sciences or healthcare, attention to detail, and knowledge of clinical trial protocols and regulations. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and reporting tools is typically required. Strong organizational skills, teamwork, and effective communication are vital soft skills for managing trial logistics and collaborating across teams. These abilities ensure the integrity, compliance, and efficiency of clinical research, ultimately supporting the development of safe and effective medical treatments.

What are some common challenges faced by part-time staff in Merck clinical trials, and how can they be addressed?

Part-time staff in Merck clinical trials often face the challenge of balancing flexible schedules with the need for consistent communication and integration within the research team. Since clinical trials require precise documentation and adherence to protocols, it's important for part-time employees to stay organized and maintain clear communication with full-time colleagues. Utilizing collaboration tools, attending regular team meetings, and proactively seeking updates can help address these challenges and ensure the part-time staff remain aligned with study goals and timelines.

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

AspectPart Time Merck Clinical TrialsPart Time Clinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldRequires a bachelor's degree, often in health sciences, nursing, or related fields
Work EnvironmentConducted within Merck's clinical trial sites or officesWorks at clinical sites, hospitals, or research facilities
Employer & IndustryPharmaceutical industry, specifically MerckHealthcare and research institutions, hospitals, or pharmaceutical companies
Job FocusAssists in trial setup, patient recruitment, and data collectionCoordinates study activities, manages patient visits, and ensures protocol adherence

While both roles support clinical research, Part Time Merck Clinical Trials focus on assisting with Merck's specific trials, whereas Part Time Clinical Research Coordinators handle broader study coordination across various organizations. Both require similar educational backgrounds and involve working in clinical settings.

What cities are hiring for Part Time Merck Clinical Trials jobs? Cities with the most Part Time Merck Clinical Trials job openings:
What are the most commonly searched types of Merck Clinical Trials jobs? The most popular types of Merck Clinical Trials jobs are:
What states have the most Part Time Merck Clinical Trials jobs? States with the most job openings for Part Time Merck Clinical Trials jobs include:
Part Time Merck Clinical Trials jobs near you

Physician - Clinical Trials - MD/DO

Headlands Research

Little Rock, AR • On-site

Full-time, Part-time

Re-posted 28 days ago

Job description

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.
Join Us in Improving Lives through Clinical Research
At Headlands Research, we're not just building a clinical trial network; we are working to bring clinical trials to underserved communities and new treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we've rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon.
Championing Diversity in Clinical Trials
Diversity isn't just a checkbox for us-it's central to our mission. We're committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.
The Role of a Lifetime
Are you ready to make a difference? We're seeking an experienced Principal Investigator or Sub-Investigator to help us grow a new clinical research site in the Little Rock area. Whether you're a seasoned Family Medicine physician or a specialist in Endocrinology, Neurology, or other area of medicine, your passion for improving patient outcomes is what matters most. If you have previous experience as an Investigator for clinical research trials, we want to talk with you. We're flexible-we're open to part-time or full-time commitments with flexible schedules.
Why Join Us?
  • Flexible Schedule: Work on your terms, with a schedule that fits your life.
  • Unlimited Potential: The sky's the limit. We're open to up to 40 hours per week, allowing you to maximize your impact.
  • Dynamic Team Environment: You'll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you'll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.

Responsibilities:
  • Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.
  • Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.
  • Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.
  • Obtain IRB approval for study initiation and any protocol modifications.
  • Oversee subject safety, trial conduct compliance, and the informed consent process.
  • Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.
  • Provide ongoing training and support to research staff.

Requirements:
  • Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.
  • Active and unencumbered license to practice as an MD or DO within the state of Arkansas required.
  • Must be board-certified or board-eligible.
  • Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.
  • Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.
  • Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.

Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind.
Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
Need Assistance?
Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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