ZipRecruiter

Log In

1

Clinical Trials Manager Jobs in Silver Spring, MD

Vivo HealthStaff

Clinical Trial Physician

Washington, DC · On-site

$110 - $140/hr

Vivo HealthStaff is recruiting for a Clinical Trials Physician for a Vaccine Trial in the USA. We are seeking an experienced and licensed Pain Management Physician to provide locum tenens coverage at ...

PharmaOut

Clinical Project Manager

Gaithersburg, MD · On-site

Participates in the planning, implementation and management of pre-IND through Phase I-II clinical trials, in collaboration with Contract Research Organization (CRO) partners, if applicable. Manage ...

Guidehouse

Clinical Program Manager

Bethesda, MD · On-site

$85K - $141K/yr

Coordinate operational and startup activities for clinical trials, including feasibility ... Develop and implement risk management strategies, including mitigation plans and resolution of ...

Guidehouse

Clinical Program Manager

Bethesda, MD · On-site

$85K - $141K/yr

Coordinate operational and startup activities for clinical trials, including feasibility ... Develop and implement risk management strategies, including mitigation plans and resolution of ...

previous pagenext page

Showing results 21-40

All JobsClinical Trials JobsClinical Trials Manager JobsClinical Trials Manager Jobs in Silver Spring, MD

Clinical Trials Manager information

See Silver Spring, MD salary details

$29

$64

$99

How much do clinical trials manager jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for clinical trials manager in Silver Spring, MD is $64.63, according to ZipRecruiter salary data. Most workers in this role earn between $52.45 and $72.79 per hour, depending on experience, location, and employer.

What does a clinical trials manager do?

A Clinical Trials Manager oversees the planning, coordination, and execution of clinical trials to ensure they are conducted safely, efficiently, and in compliance with regulatory requirements. They manage teams, budgets, timelines, and communication between stakeholders such as sponsors, investigators, and regulatory bodies. Their responsibilities also include monitoring trial progress, resolving issues, and ensuring data integrity throughout the study.

What are some common challenges faced by clinical trials managers and how can they be addressed?

Clinical Trials Managers often encounter challenges such as ensuring regulatory compliance, managing complex timelines, and coordinating communication among diverse stakeholders. Balancing the needs of sponsors, investigators, and regulatory bodies requires strong organizational skills and attention to detail. Proactively addressing these challenges involves implementing robust project management tools, maintaining clear documentation, and fostering open communication within the team. Building relationships with site staff and regularly updating all parties can help anticipate issues early and keep trials on track.

What are the key skills and qualifications needed to thrive as a clinical trials manager, and why are they important?

To thrive as a Clinical Trials Manager, you need expertise in clinical research processes, regulatory compliance, and project management, often supported by a degree in life sciences and experience in clinical trial coordination. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications such as ACRP or SOCRA are typically required. Strong leadership, attention to detail, and effective communication are vital soft skills for managing teams and ensuring protocol adherence. These skills and qualities are crucial for maintaining trial integrity, regulatory compliance, and successful project outcomes.

What is the difference between Clinical Trials Manager vs Clinical Research Coordinator?

AspectClinical Trials ManagerClinical Research Coordinator
ResponsibilitiesOversees entire clinical trial process, manages teams, ensures compliance, and handles budgets.Assists with patient recruitment, data collection, and site coordination under supervision.
Required CredentialsBachelor’s or higher in life sciences, often with project management experience.Typically holds a bachelor’s degree in health sciences or related field; certification may be preferred.
Work EnvironmentWorks in clinical trial sites, research organizations, or pharmaceutical companies.Primarily works at clinical sites, hospitals, or research facilities.

In summary, Clinical Trials Managers oversee the entire trial process and manage teams, while Clinical Research Coordinators support daily trial activities at the site level. Both roles require relevant education and work in clinical research settings, but differ in scope and responsibilities.

What are the most commonly searched types of Clinical Trials jobs in Silver Spring, MD?

The most popular types of Clinical Trials jobs in Silver Spring, MD are:

What are popular job titles related to Clinical Trials Manager jobs in Silver Spring, MD?

For Clinical Trials Manager jobs in Silver Spring, MD, the most frequently searched job titles are:

What job categories do people searching Clinical Trials Manager jobs in Silver Spring, MD look for?

The top searched job categories for Clinical Trials Manager jobs in Silver Spring, MD are:

What cities near Silver Spring, MD are hiring for Clinical Trials Manager jobs?

Cities near Silver Spring, MD with the most Clinical Trials Manager job openings:

Clinical Trials Manager jobs near you
Infographic showing various Clinical Trials Manager job openings in Silver Spring, MD as of August 2026, with employment types broken down into 90% Full Time, 9% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $134,426 per year, or $64.6 per hour.

Clinical Trial Recruitment Specialist

Pharmaron

Baltimore, MD • On-site

$20 - $22/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 7 days ago

Job description

Position: Clinical Trial Recruitment Specialist

Salary Range: $20.00/hr.- $22.00/hr.

Location: Baltimore, MD (On-site)

About Pharmaron

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.

We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit www.pharmaron.com.

Job Overview

The Clinical Trial Recruitment Specialist is responsible for ensuring volunteer participation for each clinical study.

Key Responsibilities

  • Recruitment Operations
    • Pre-screens potential participants to ensure they meet protocol-specific inclusion/exclusion criteria and understand the study details.
    • Manages and updates the Recruitment Database of study volunteers.
    • Creates and maintains the participant screening appointment schedule.
    • Sends informed consent (ICF) videos to participants prior to telehealth appointments.
  • Participant Screening & Protocol Compliance
    • Conduct telehealth procedures including informed consent, demographic collection, medical history review, and assessment of protocol eligibility.
    • Maintains thorough knowledge of inclusion/exclusion criteria for all active protocols.
    • Ensures strict adherence to protocol guidelines and Good Clinical Practices (GCPs).
  • Collaboration & Outreach
    • Collaborates with internal staff to ensure seamless participant service.
    • Partners with community organizations and participate in events to educate and recruit potential clinical trial participants.
  • Quality Assurance
    • Reviews participant data to confirm alignment with protocol requirements

  What We're Looking For:

  • Associates degree OR equivalent combination of education and experience.
  • One year of relevant work experience may be substituted for one year of required education.
  • At least 1 year of call center experience

Why Pharmaron?

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.

Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:

  • Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
  • 401(k) Retirement Plan with generous employer matching
  • Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
  • Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
  • Employee Assistance Program (EAP), mental health resources, and wellness programs
  • Family-friendly benefits, including fertility support and maternity resources
  • Professional development and career growth opportunities within a leading global CRO/CDMO

How to Apply:

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.

#LI-KS1

Apply