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Full Time Clinical Research Associate Jobs in Silver Spring, MD

Guidehouse

Clinical Research Coordinator

Bethesda, MD ยท On-site

$65K - $108K/yr

We are seeking a Clinical Research Coordinator to provide comprehensive clinical research ... This is a full-time, on-site role in Bethesda, MD. * Provide guidance and operational training to ...

Guidehouse

Clinical Research Coordinator

Bethesda, MD

$65K - $108K/yr

We are seeking a Clinical Research Coordinator to provide comprehensive clinical research ... This is a full-time, on-site role in Bethesda, MD. * Provide guidance and operational training to ...

ObjectiveHealth

Clinical Research Coordinator I

Laurel, MD ยท On-site

$24 - $32/hr

Clinical Research Coordinator I Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate will possess ...

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All JobsClinical Research Associate JobsFull Time Clinical Research Associate JobsFull Time Clinical Research Associate Jobs in Silver Spring, MD

Full Time Clinical Research Associate information

See Silver Spring, MD salary details

$37.2K

$97.5K

$148.3K

How much do full time clinical research associate jobs pay per year?

As of Aug 8, 2026, the average yearly pay for full time clinical research associate in Silver Spring, MD is $97,500.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,600.00 and $132,300.00 per year, depending on experience, location, and employer.

What are some common challenges faced by full time clinical research associates when managing multiple clinical trials simultaneously?

Full Time Clinical Research Associates (CRAs) often juggle several studies at once, which can make prioritizing tasks and managing time effectively a challenge. Staying compliant with regulatory requirements while ensuring data accuracy and maintaining clear communication with site staff requires strong organizational skills. Additionally, frequent travel and adapting to different site environments can be demanding. CRAs who develop robust planning strategies and effective communication habits tend to navigate these challenges successfully, ensuring studies run smoothly and efficiently.

What is a full time clinical research associate?

A Full Time Clinical Research Associate (CRA) is a professional responsible for monitoring clinical trials and ensuring that research studies comply with regulatory requirements and study protocols. CRAs play a critical role in the development of new drugs and medical devices by overseeing the progress of clinical trials, verifying data accuracy, and ensuring patient safety. They often travel to various clinical sites to conduct site visits, train staff, and review study documentation. Working full time, a CRA may handle multiple studies simultaneously and collaborate closely with investigators, sponsors, and regulatory agencies.

What are the key skills and qualifications needed to thrive as a full time clinical research associate?

To thrive as a Full Time Clinical Research Associate, you need a solid background in life sciences or a related field, familiarity with Good Clinical Practice (GCP) guidelines, and a bachelor's degree (often required). Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and understanding of regulatory requirements is crucial, and certifications like ACRP or SOCRA are often valued. Strong attention to detail, communication, and organizational skills help you effectively monitor trials and collaborate with study sites. These competencies ensure that clinical trials are conducted ethically, efficiently, and in compliance with regulatory standards, which is vital for patient safety and reliable research outcomes.

What is the difference between Full Time Clinical Research Associate vs Clinical Research Coordinator?

AspectFull Time Clinical Research AssociateClinical Research Coordinator
CredentialsBachelor's degree, often with clinical or life sciences background; certifications like CCRP or ACRP are commonBachelor's degree in health sciences or related field; certifications like CCRP or ACRP are also common
Work EnvironmentMonitor clinical trials at multiple sites, often traveling; work closely with sponsors and CROsManage daily trial activities at a single site; coordinate with investigators and staff
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites, academic institutions

While both roles require similar educational backgrounds and certifications, a Full Time Clinical Research Associate primarily monitors multiple trial sites and ensures compliance, often traveling. In contrast, a Clinical Research Coordinator manages trial activities at a single site, focusing on patient recruitment and data collection. Both roles are essential in clinical research but differ in scope and daily responsibilities.

What are popular job titles related to Full Time Clinical Research Associate jobs in Silver Spring, MD? For Full Time Clinical Research Associate jobs in Silver Spring, MD, the most frequently searched job titles are:
What job categories do people searching Full Time Clinical Research Associate jobs in Silver Spring, MD look for? The top searched job categories for Full Time Clinical Research Associate jobs in Silver Spring, MD are:
Full Time Clinical Research Associate jobs near you

Clinical Research Coordinator III

Alaka'ina Foundation Family of Companies

Silver Spring, MD โ€ข On-site

$25 - $33.25/hr

Full-time

Medical, Dental, Life, Retirement, PTO

Re-posted 11 days ago

Job description

Bering-Alaka`ina Holdings, LLC is looking for a Clinical Research Coordinator to support our government customer in Silver Spring, Maryland.
DESCRIPTION OF RESPONSIBILITIES:
  • Organize and prioritize all activities associated with conducting phase 1, 2, and 3 clinical and operational research studies within a military clinic setting.
  • Review and understand research protocols, ensuring applicable regulations, and guidelines are followed.
  • Coordinate space and supplies with appropriate personnel.
  • Recruit volunteers for the studies, to include determining volunteer population availability, advertising venues, and discussions with potential volunteers via telephone or e-mail.
  • Serve as a Volunteer advocate and associated duties.
  • Maintain study/test article accountability and administration.
  • Gather, prepare, and maintain appropriate information and documentation per applicable FDA regulations and ICH guidelines (e.g., source and case report forms, participant rosters, SOPs, etc.)
  • Enter required data on CRFs and audit records for accuracy, resolve discrepancies, and correct as necessary.
  • Coordinate with external and internal monitors.
  • Assist in training research staff on protocol-related study methods.
  • Monitor study data collection procedures to ensure uniformly high levels of compliance with GCP, GLP, FDA and other government- or locally-required guidances.
  • Able to design and create forms, reports, etc.
  • Maintain a safe workplace, observing appropriate safety and occupational health rules and regulations. Attend safety training relative to the position and report any infractions of safety procedures to the facility Safety Officer.
  • Other duties as assigned.

REQUIRED DEGREE/EDUCATION/CERTIFICATION:
  • Required to be a Registered Nurse licensed to practice in the state of Maryland, who are skilled and qualified in nursing procedures to include, but not limited to phlebotomy and the administration of experimental vaccines and other parenteral therapeutics as per specific protocol guidance in accordance with the 21 Code of Federal Regulation (CFR) 11, 50, 54, 56, 312, and 314.
  • Basic Life Support (BLS -CPR/AED) certification.
  • Maintain Certification in Clinical Research Coordination by Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA)

REQUIRED SKILLS AND EXPERIENCE:
  • Four (4) years clinical trials experience.
  • Five (5) years of experience in clinical research coordination, with expertise in FDA-regulated trials.
  • Experience facilitating clinical monitoring visits and resolving inquires.
  • Experience utilizing clinical trial management systems and databases (e.g., REDcap and Inform).
  • Must be able to work both independently and in a team setting.
  • Must have excellent communication, organization, and prioritization skills.
  • Intermittent physical activity including bending, reaching, and prolonged periods of sitting and or standing.
  • May be required to work at any facility and be responsible for own transportation.
  • Will be scheduled based on operational and business needs.
  • Required Knowledge, Skills and Abilities; knowledge of applicable highly complex scientific procedures and techniques relating to position.
  • Physical Capabilities: work may involve long periods of standing and handling of numerous chemicals and/or hazardous biological material.
  • Work Environment: Clinic/laboratory environment; may require working evenings and weekends.
  • Must be able to work independently and mentor other Clinic staff.
  • Must be able to work independently following a brief period of specific technical training.
  • Ability to establish and maintain effective working relationships with coworkers, managers and customers.

DESIRED SKILLS AND EXPERIENCE:
  • Advanced Cardiac Life Support (ACLS) certification encouraged.
  • Certification in clinical research (e.g., CCRP or CCRA) is preferred.
  • Commission for Case Manager Certification (CCMC) certification preferred.

REQUIRED CITIZENSHIP AND CLEARANCE:
A Tier I background investigation will be required.
Bering-Alaka`ina Holdings, LLC is a fast-growing government service provider. Employees enjoy competitive salaries. Eligible employees enjoy a 401K plan with company match; medical, dental, disability, and life insurance coverage; tuition reimbursement; paid time off; and 11 paid holidays.
We are an Equal Opportunity/Affirmative Action Employer of individuals with disabilities and veterans. We are proud to state that we do not illegally discriminate in employment decisions on the basis of any protected categories. If you are a person with a disability and you need an accommodation during the application process, please click here to request accommodation. We E-Verify all employees
"EOE, including Disability/Vets" OR "Equal Opportunity Employer, including Disability/Veterans"
Bering-Alaka`ina Holdings, LLC is comprised of industry-recognized government service firms designated as Alaska Native Corporation (ACN)-owned and 8(a) certified businesses and includes Ke`aki Technologies, LLC; Laulima Government Solutions, LLC; Kลซpono Government Services, LLC; Kapili Services, LLC; Po`okela Solutions, LLC; Kฤซkaha Solutions, LLC; and Pololei Solutions, LLC.
For additional information, please visit www.beringalakaina.com
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