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Protocol Coordinator Jobs in Silver Spring, MD (NOW HIRING)

Cape Fox Corporation

Research Nurse

Bethesda, MD · On-site

$55/hr

Participate in the planning and execution of clinical research in the capacity of clinical support staff and Protocol Coordinator; support research assistants in the scheduling, follow-up, and ...

IQVIA

Research Coordinator

Fairfax, VA

Research Coordinators attend study teleconferences with sponsors and clinical research ... Protocol Compliance * Identifies primary and secondary study objectives and outcome measures

IQVIA

Research Coordinator

Fairfax, VA

Research Coordinators attend study teleconferences with sponsors and clinical research ... Protocol Compliance * Identifies primary and secondary study objectives and outcome measures

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Studio Coordinator

Arlington, VA · On-site

$15 - $19.50/hr

... protocol execution, front desk guidance, and team support - Must be flexible with schedule ... coordination of the Studio Experience Team (SET) including shift scheduling, stepping in for no ...

CorePower Yoga

Studio Coordinator

Arlington, VA · On-site

$15 - $19.50/hr

... protocol execution, front desk guidance, and team support - Must be flexible with schedule ... coordination of the Studio Experience Team (SET) including shift scheduling, stepping in for no ...

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Studio Coordinator

Arlington, VA · On-site

$15 - $19.50/hr

... protocol execution, front desk guidance, and team support - Must be flexible with schedule ... coordination of the Studio Experience Team (SET) including shift scheduling, stepping in for no ...

RWD Consulting

Simulation Event Coordinator

Bethesda, MD · On-site

$70K/yr

Maintains regulations, directives and pertinent information on visitor(s) protocol, to include ... Coordinates efforts with Contractor, Service Chiefs, and Department Chiefs, Staff Officers, the ...

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Protocol Coordinator information

See Silver Spring, MD salary details

$27.9K

$59.8K

$104.9K

How much do protocol coordinator jobs pay per year?

As of Aug 22, 2026, the average yearly pay for protocol coordinator in Silver Spring, MD is $59,823.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,900.00 and $71,800.00 per year, depending on experience, location, and employer.

What is a protocol coordinator?

Protocol coordinators are professionals responsible for managing and overseeing the implementation of clinical trial protocols or research studies. They ensure that all activities are conducted in compliance with regulatory requirements, ethical standards, and the specific guidelines of the study protocol. Their duties often include organizing study logistics, coordinating communications between investigators and sponsors, maintaining accurate documentation, and ensuring participant safety. Protocol coordinators play a crucial role in ensuring the smooth and efficient operation of clinical research projects.

What are the key skills and qualifications needed to thrive as a protocol coordinator, and why are they important?

To thrive as a Protocol Coordinator, you need strong organizational skills, attention to detail, and a background in clinical research or project management, often supported by a relevant bachelor's degree. Familiarity with regulatory compliance systems, clinical trial management software (CTMS), and protocols such as Good Clinical Practice (GCP) is typically required. Excellent communication, problem-solving, and multitasking abilities help you effectively coordinate between stakeholders and manage complex timelines. These skills ensure the smooth execution of protocols, regulatory compliance, and the successful progression of clinical studies or organizational processes.

What are some common challenges protocol coordinators face when managing complex meetings or events?

Protocol Coordinators often encounter challenges such as balancing the needs and expectations of diverse stakeholders, ensuring strict adherence to diplomatic protocols, and managing last-minute changes in schedules or guest lists. Successfully navigating cultural sensitivities and maintaining effective communication with both internal teams and external partners are key to overcoming these obstacles. Flexibility, attention to detail, and strong organizational skills are essential for addressing unexpected issues while maintaining a professional environment.

What is the difference between Protocol Coordinator vs Clinical Research Associate?

AspectProtocol CoordinatorClinical Research Associate
Required CredentialsTypically a bachelor's degree in health sciences, life sciences, or related field; certifications like CCRP are a plusUsually a bachelor's degree in life sciences or health sciences; certifications like CCRP or CRA are common
Work EnvironmentOffice-based, coordinating clinical trial protocols, communicating with sites and teamsMonitoring clinical sites, ensuring compliance, and data accuracy during trials
Employer & Industry UsagePharmaceutical companies, research institutions, CROsPharmaceutical companies, CROs, research organizations

While both roles support clinical trials, Protocol Coordinators focus on managing trial protocols and communication, whereas Clinical Research Associates primarily monitor trial sites and ensure compliance. Both roles require similar educational backgrounds and certifications, often working within the same industry environments.

How long does it take to become a protocol coordinator?

Becoming a protocol coordinator typically requires a bachelor's degree in a related field such as healthcare, life sciences, or research, which takes about four years. Gaining relevant experience in clinical research or project management can take an additional 1-3 years, depending on the individual's background and the complexity of the role.

What are popular job titles related to Protocol Coordinator jobs in Silver Spring, MD?

For Protocol Coordinator jobs in Silver Spring, MD, the most frequently searched job titles are:

What job categories do people searching Protocol Coordinator jobs in Silver Spring, MD look for?

The top searched job categories for Protocol Coordinator jobs in Silver Spring, MD are:

What cities near Silver Spring, MD are hiring for Protocol Coordinator jobs?

Cities near Silver Spring, MD with the most Protocol Coordinator job openings:

Protocol Coordinator jobs near you
Infographic showing various Protocol Coordinator job openings in Silver Spring, MD as of August 2026, with employment types broken down into 83% Full Time, and 17% Part Time. Highlights an 100% In-person job distribution, with an average salary of $59,823 per year, or $28.8 per hour.

Research Nurse

Cape Fox Corporation

Bethesda, MD • On-site

$55/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 14 days ago

Job description

Job Title
Research Nurse
Job Description
Concentric Methods is seeking an experienced Research Nurse to independently provide support services to satisfy the overall operational objectives of the National Institute of Mental Health. The primary objective is to provide services and deliverables through performance of support services.
The total hourly pay for this exempt position is $55.00 for up to 40 hours per week. This rate represents the company's good faith and reasonable estimate of possible compensation at the time of posting. In addition, for eligible positions we offer a variety of benefits including specified holidays, paid leave, health insurance, dental insurance, vision insurance, life and disability insurance, tuition reimbursement, as well as 401K with company match. This job will be posted until filled or withdrawn.
Duties include:
  • Facilitate screening patients for the projects that focus on adolescents with major depressive disorder.
  • Screen for studies on Major Depression:
  • Respond to parents and teens who contact NIMH expressing interest in research participation; explain the nature of the research studies; provide guidance on how to complete preliminary screening using secure, on-line methods or hardcopy responses to screening questions; provide log-in passwords and review files to ascertain that questionnaires have been completed.
  • Identify safety risks during assessment such as imminent suicidal ideation or behavior, ongoing substance abuse, psychosis, self-injury in response to interpersonal conflict, child abuse, recent physical or sexual trauma.
  • Conduct accurate preliminary evaluation of potential probands through telephone interviewing of parent, review of medical records, consultation with treating professionals, and consultation with NIMH medical staff, leading to acceptance for onsite evaluation or rejection with referral if indicated.
  • Conduct structured and semi-structured interviews with probands, and parents and siblings of probands; perform semi-structured interviews of parents to determine family medical and psychiatric history.
  • Conduct screening/baseline evaluations in collaboration with staff.
  • Administer and score a wide range of structured and semi-structured interviews (such as the SCID, the K-SADS and many others) to the child and adolescent probands and the parents of the probands.
  • Support for Research with participants in Screening, Longitudinal, and Treatment Studies:
  • Provide family support and crisis management services as needed.
  • Provide clinical support to patients and families throughout the time that they are participating in research protocols.
  • Provide referral to appropriate NIH resources and community services, when indicated.
  • Participate in the planning and execution of clinical research in the capacity of clinical support staff and Protocol Coordinator; support research assistants in the scheduling, follow-up, and tracking of participants in research.
  • Make recommendations for appropriate referrals, including Child Protective Services, psychotherapy, community services involvement, special education, or activity programs.
  • Document clinical contacts and findings; enter clinically relevant research information.
  • Participate in research group meetings and in the decision-making process regarding patient inclusion in the studies, patient and parent diagnosis, and patient and family management throughout participation in the research protocol.
  • Locate, evaluate and maintain contact with community organizations and facilities such as day treatment centers, clinics. Support MRI and MEG research procedures; evaluate the appropriateness of a subject for participation in brain imaging research; conduct a clinical assessment concerning the
  • degree to which a child, adolescent, or adult meets safety criteria for entering a magnetic resonance imaging (MRI) or magnetoencephalography (MEG) environment.
  • Assist children, adolescents, and adults receiving a MEG or MRI examinations; assist staff as they prepare patients for a brain imaging studies; alert the staff to safety concerns during this process; attach physiology monitoring equipment to a patient in an MRI environment.

Travel Requirements
0 - 10%
Job Requirements
  • Masters degree in Nursing with current state licensure
  • Minimum of six (6) years of related experience
  • CPR Certification
  • Experience in clinical research setting with protocols and clinical trials - Experience providing clinical services in a medical setting
  • Experience with Microsoft Office Suite
  • Strong communications skills, both oral and written
  • Excellent analytical, organizational and time management skills

Cape Fox Corporation, its subsidiaries and affiliates provide equal employment opportunities to all persons and prohibit employment decisions on the basis of race, religion, color, creed, national origin, sex, age, disability, political affiliation, protected veteran status, or sexual orientation. Cape Fox Corporation, its subsidiaries and affiliates offer preference to Cape Fox
Category
Healthcare
Location
NIH - Bethesda, MD - Rockville, MD 20892 US (Primary)
Education
Master's Degree

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