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Part Time Merck Clinical Trials Jobs (NOW HIRING)

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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 Jun 11, 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 are Part Time Merck Clinical Trials jobs?

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, and why are they important?

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.

Is it hard to get a job at Merck?

Securing a part-time clinical trials position at Merck can be competitive, often requiring relevant education, experience, or certifications in healthcare or research. Candidates should demonstrate strong attention to detail, compliance with regulatory standards, and familiarity with clinical trial protocols to improve their chances.

Does Merck offer flexible remote work options?

Part Time Merck Clinical Trials positions may offer flexible work arrangements, including remote options, depending on the specific role and department. Candidates should review the job description or contact Merck's HR for details on remote work policies and schedule flexibility.

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.

How much do Merck clinical trial managers make?

Clinical trial managers at Merck typically earn between $80,000 and $130,000 annually, depending on experience, location, and level of responsibility. They often require knowledge of clinical research processes, regulatory compliance, and project management tools.

Which clinical trial jobs pay the most?

In clinical trials, roles such as Clinical Research Directors, Principal Investigators, and Clinical Trial Managers tend to have the highest salaries due to their experience and responsibilities. Positions requiring advanced degrees, certifications, and leadership skills generally offer higher pay, especially in larger organizations or for trials with complex protocols.
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:
Clinical Research Gastroenterologist - Chicago, IL (Part Time)

Clinical Research Gastroenterologist - Chicago, IL (Part Time)

ProTouch Staffing

Chicago, IL

Part-time

Posted 9 days ago


Job description

Clinical Research Gastroenterologist - Chicago, IL 
Part-Time (0-8 hours/week)

Key Responsibilities
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials.
Provide clinical oversight and ensure adherence to study protocols, ICH-GCP, and regulatory standards.
Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.
Qualifications
M.D. or D.O. with an active, unrestricted Illinois medical license.
Board Certification in Gastroenterology.
Valid DEA license and BLS/ACLS certification.
Clinical research/clinical trials experience preferred (training available for motivated candidates).
Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS).
Benefits
Flexible, part-time schedule (0-8 hours per week).
Opportunity to expand expertise in multi-therapeutic clinical trials.
Direct involvement in advancing innovative treatments through research.

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