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Entry Level Clinical Research Associate Jobs in Silver Spring, MD

Research Nurse

Baltimore, MD · On-site

$45 - $50/hr

Associate's degree in Nursing with current state nursing license. * Minimum of 2 years of nursing experience with CPR certification. * Experience in a clinical research environment. * Knowledge of ...

Research Nurse

Baltimore, MD · On-site

$45 - $50/hr

Associate's degree in Nursing with current state nursing license. * Minimum of 2 years of nursing experience with CPR certification. * Experience in a clinical research environment. * Knowledge of ...

Research Nurse

Baltimore, MD · On-site

$45 - $50/hr

Associate's degree in Nursing with current state nursing license Minimum of 2 years of nursing experience with CPR certification. Experience in a clinical research environment. Knowledge of clinical ...

Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities.

Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities.

This is an excellent opportunity for individuals looking to gain entry-level experience in clinical research while making a direct impact on studies that advance global health. You'll work closely ...

Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities.

This is an excellent opportunity for individuals looking to gain entry-level experience in clinical research while making a direct impact on studies that advance global health. You'll work closely ...

Job Overview The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities.

Study Start-Up Associate II

Rockville, MD · Remote

$34.25 - $46.75/hr

Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all ... Emmes Group is transforming the future of clinical research, bringing the promise of new medical ...

Showing results 41-60

Entry Level Clinical Research Associate information

What are the typical daily responsibilities of an entry level clinical research associate?

As an Entry Level Clinical Research Associate, your day-to-day work generally involves assisting with monitoring clinical trial sites, reviewing study documentation, and ensuring adherence to protocol and regulatory requirements. You may support more senior team members in conducting on-site or remote visits, tracking patient recruitment, and managing data collection. Additionally, you’ll communicate regularly with site staff and other stakeholders to resolve issues and ensure data quality. This hands-on experience is essential for building expertise in clinical research processes and advancing toward more senior CRA roles.

What is an entry level clinical research associate?

An Entry Level Clinical Research Associate (CRA) is responsible for monitoring clinical trials to ensure compliance with regulatory requirements, ethical guidelines, and study protocols. They assist in site selection, data collection, and verifying that study procedures are properly followed. Entry-level CRAs typically work under the supervision of senior CRAs and may travel to different clinical sites. Strong attention to detail, knowledge of Good Clinical Practice (GCP) guidelines, and organizational skills are essential. This role is a starting point for a career in clinical research, with opportunities for growth into senior CRA or project management positions.

What are the key skills and qualifications needed to thrive as an entry level clinical research associate?

To thrive as an Entry Level Clinical Research Associate, you typically need a bachelor's degree in life sciences or a related field, a solid understanding of clinical trial protocols, and attention to detail. Familiarity with Good Clinical Practice (GCP) guidelines, electronic data capture (EDC) systems, and regulatory documentation is often required. Strong communication, organization, and problem-solving abilities help you effectively collaborate with study sites and team members. These skills are critical to ensure the accuracy, compliance, and successful progression of clinical studies.

What are the most commonly searched types of Entry Level Clinical Research jobs in Silver Spring, MD? The most popular types of Entry Level Clinical Research jobs in Silver Spring, MD are:
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Infographic showing various Entry Level Clinical Research Associate job openings in Silver Spring, MD as of July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

$45 - $50/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago


Job description

Job Title
Research Nurse
Job Description
Concentric Methods is seeking a Research Nurse to join our team in Baltimore, MD in support of the NIH.
Responsibilities:

  • Recruits and screens patients for inclusion in protocols and clinical trials.
  • Assist research and medical staff interview, screen and evaluate the appropriateness of eligible subjects for participation in the research protocol
  • Recruit and follow up with patients for clinical and basic research studies and protocols and provide clinical support to patients participating in protocol
  • Provide instruction to potential clinical study subjects and those involved in care of subjects on aspects of subjects care, treatments, and side-effects
  • Performs assessments and physicals, and collects medical histories.
  • Participate in direct patient care, in coordination with interdisciplinary team and specific team members to create and communicate a plan of care that balances clinical care needs with research
  • Obtain and record complete health histories and conduct physical assessments; communicate data from these and other sources
  • Manage clinical and research support activities to ensure patient safety and address the clinical needs of the patients
  • Administers protocol consents and documentation and monitors compliance.
  • Ensure informed consent process and human subjects protection in clinical research and counsel patients regarding the potential risks
  • Collaborate with researchers and medical staff to obtain and maintain informed consent and assent and address ethical and legal implication of the research protocol
  • Performs data input and management.
  • Perform accurate data entry into research database, including the use of standardized scales and assessments
  • Examine and monitor patients during protocol studies; ensure the collection of a complete clinical database on each patient
  • Performs clinical data interpretation and evaluates and interprets protocol and clinical trial findings.
  • Participate in clinical practice and research support meetings and develop multidisciplinary performance improvement programs and projects to improve operating procedures, patient care and decrease costs
  • Participates in training and mentoring new staff
  • Provide mentorship developing skills and expertise in research protocols and all aspects of clinical research
  • Develops new research protocols
  • Work with staff on drafting of new protocol amendments and associated documents by providing editorial support and expert opinion
Travel Requirements
0 - 10%
Job Requirements
  • Associate's degree in Nursing with current state nursing license.
  • Minimum of 2 years of nursing experience with CPR certification.
  • Experience in a clinical research environment.
  • Knowledge of clinical research data collection and clinical data report preparation.
  • Working knowledge of ICH-GCPs.
  • Knowledge of the principles, theories, techniques and practices of general nursing.
  • Demonstrated expertise in data management.
  • Ability to coordinate various activities (research subject schedules, data and biospecimen collection and nursing care) to ensure proper and timely filing of standard clinical/regulatory documentation, serious adverse events, amendments, annual reports and other regulatory documents.
  • Ability to participate in efforts to ensure scientific quality and human subjects' protection.
  • Ability to oversee ongoing protocol operations to ensure study compliance; troubleshoot possible protocol violations.
  • Knowledge of Microsoft Office Suite (MS Word, Excel, Outlook) and other spreadsheet applications.
  • Strong communications skills, both oral and written.
  • Excellent analytical, organizational and time management skills.

The total hourly pay for this exempt position is $45.00/hr. to $50.00/hr. 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.
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 Corporation shareholders, descendants and other Native Americans pursuant to Public Law 100-241.
Category
Healthcare
Location
NIH - Baltimore, MD - Baltimore, MD 21224 US (Primary)
Education
Associate's Degree