Clinical Research Associate Jobs in Maryland, United States

Senior Clinical Research Associate with 2+ years on‑site monitoring experience. Conduct site monitoring, recruitment tracking, protocol training, and regulatory submissions.

AstraZeneca seeks a Clinical Research & Development Associate Director in Gaithersburg, Maryland, to drive the development of novel therapies for inflammatory myopathies and related diseases. The role integrates clinical, scientific, and commercial expertise to oversee study design, execution, and lifecycle management while mentoring staff.

<p style="text-align:left"><b>Job Description</b></p><p style="text-align:inherit"></p><p><b><u>CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS</u>: ALABAMA, GEORGIA, COLORADO, MASSACHUSETTS, MICHIGAN, MARYLAND, PENNSYLVANIA</b></p><p></p><p>The role is accountable for performance and compliance for assigned protocols and sites in a country.</p><p></p><p>Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company

AstraZeneca seeks an Associate Principal Scientist in Gaithersburg, Maryland, to lead clinical R&D for inflammatory myopathies and autoimmune diseases. The role involves guiding full lifecycle drug development, managing cross-functional teams, and ensuring regulatory compliance.

Clinical Research team at Merck conducts oncology trials across the US. The Clinical Research Associate manages site relationships, ensures protocol compliance, performs remote and on‑site monitoring, and collaborates with cross‑functional groups to drive study performance. Remote work, candidates must reside in listed states, travel 65‑75% of time, 2‑3 days/week on site.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate manages site activities for rare CNS studies, conducts initiation visits, ensures regulatory compliance, and supports contract and budget negotiations.

Fortrea's FSP team is hiring experienced Clinical Research Associates (CRAs) specializing in Ophthalmology monitoring across major US hub locations. The role involves full-cycle study site monitoring, CRF review, SAE reporting, and ensuring participant safety and data integrity in a fast-paced, technology-driven clinical research environment.

AstraZeneca seeks a Clinical Research & Development Associate Director for Myositis/Immunology in Gaithersburg, Maryland. This role drives the development of novel therapeutics for inflammatory myopathies and autoimmune diseases by integrating scientific, commercial, and operational strategies.

Evinova, a health-tech business within the AstraZeneca Group, accelerates better health outcomes by embedding digital health at scale across R&D, with Oncology as a key therapeutic area. The Associate Director in the Quantitative COA Science team provides quantitative measurement support for patient-centered measurement strategy, including selection of data collection strategies, development of patient-centric endpoints, evidence strategy, and design and interpretation of data analyses for disse

Join a global clinical research organization that has supported the top 50 pharmaceutical companies and 750+ biotechs across 2,700 trials in 100+ countries. As an Assistant Clinical Research Associate, you will perform remote activities on assigned projects in liaison with the CRA and study Clinical Lead, providing support with site preparedness, logistical support to the monitoring process, and assisting with site management and remote monitoring tasks per SOPs and regulatory guidelines.

Parexel’s Clinical Research Physician (Early Phase Clinical Unit) role in Baltimore, Maryland, invites a team‑oriented physician to lead investigator responsibilities across early phase studies. The position is full‑time, onsite Monday‑Friday with daytime hours and weekend on‑call rotations every 3‑4 weekends.

National Institute of Neurological Disorders and Stroke (NINDS) team at NIH coordinates patient recruitment, scheduling, travel, and inpatient/outpatient admissions for clinical studies. The coordinator manages protocol documentation, regulatory binders, and data collection while acting as a liaison between patients, families, and research staff.

Clinical Research team at U.S. Dermatology Partners conducts outpatient clinical trials for dermatology treatments. The Coordinator I schedules and conducts patient visits, collects vitals, phlebotomy, EKG, and investigational drug administration, enters source data into EDC, and maintains regulatory documents while coordinating with IRBs, sponsors, and labs.

The Geneva Foundation’s Clinical Research Manager leads on‑site operations for the RION Phase 1b study, overseeing trial conduct, recruitment, and regulatory compliance. The role manages staff, coordinates site initiation and safety reviews, and ensures adherence to FDA and GCP standards.

The American Red Cross seeks an Analyst I, Clinical Research to support its humanitarian mission by managing clinical study data and sample documentation. In this on-site role in Rockville, MD, you will independently perform daily enrollment activities, validate laboratory results, and generate research reports while collaborating with team members.

Alaka`ina Foundation Clinical Research team conducts phase 1-3 clinical trials in a military clinic setting. The Clinical Research Coordinator III manages study protocols, recruits volunteers, ensures FDA/ICH compliance, enters data, and mentors staff.

AstraZeneca seeks a Clinical Research & Development Director in Gaithersburg, Maryland, to drive integrated clinical research strategies for autoimmune diseases. The role involves leading cross-functional teams, managing budgets and risks, and overseeing regulatory submissions to ensure drug development success.

Professional Services team at Axle supports NIH research initiatives, focusing on clinical studies within the National Institute on Drug Abuse. The Clinical Research Coordinator manages participant recruitment, consent, data collection, and regulatory documentation, and assists with scheduling, travel arrangements, and sample handling.

CenExel Clinical Research coordinates multi-site clinical trials to advance CNS and early phase studies. The Coordinator assists with patient involvement, data collection, regulatory documentation, and safety assessments while ensuring compliance with ICH and GCP standards.

Professional Services team at Axle supports translational research and biomedical informatics for NIH and NCI. The Clinical Research Coordinator manages complex clinical study portfolios, overseeing protocol development, regulatory submissions, budgeting, and multi‑site coordination while reporting progress to leadership. Bethesda, MD, on-site, Full-time, relocation assistance offered.