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Part Time Merck Clinical Trials Jobs (NOW HIRING)

Access Community Clinical Trials

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Clinical Research Nurse

Abilene, TX · On-site

Abilene, Texas Employment Type: Part-Time Access Community Clinical Trials (ACCT) is a growing clinical research organization dedicated to expanding access to high-quality clinical trials within ...

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

As of Jun 10, 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.

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

Clinical Trials Recruiter

NY SCIENTIFIC CORP

Brooklyn, NY • On-site, Remote

$20 - $30/hr

Part-time

Posted 13 days ago

Job description

Job Title: Clinical Trials Recruiter
Location: Brooklyn, NY / [On-site and  Remote]
Compensation: based on experience
Job Type: [Part-time but potential to become full-time]. 
About Us
We are a dedicated clinical research site committed to advancing medical knowledge through high-quality clinical trials. Our mission is to connect patients with innovative treatment opportunities while upholding the highest ethical and professional standards.
Position Overview
We are seeking a motivated and detail-oriented Clinical Trials Recruiter to join our team. The recruiter will be responsible for identifying, engaging, and enrolling eligible participants into ongoing clinical studies. This role requires excellent communication skills, professionalism, and the ability to build trust with potential participants.
Key Responsibilities

  • Conduct outreach to potential participants through phone calls, emails, social media, and community events.
  • Screen participants for eligibility based on study protocols.
  • Maintain accurate records of recruitment activities and participant status.
  • Collaborate with study coordinators and investigators to ensure smooth enrollment.
  • Develop and implement creative strategies to meet recruitment targets.
  • Provide information to participants about clinical trials in a clear, ethical, and compassionate manner.
Qualifications

  • Previous experience in patient recruitment, sales, customer service, or healthcare preferred.
  • Strong communication and interpersonal skills.
  • Ability to work independently and meet recruitment goals.
  • Organized, detail-oriented, and comfortable using databases/CRM systems.
  • Knowledge of clinical research processes is a plus, but training will be provided