Clinical Trial Manager Jobs in Maryland
A Clinical Trial Manager in the biotechnology industry oversees the planning, implementation, and completion of clinical trials. They are crucial in ensuring that trials are conducted in a way that ensures patient safety, data integrity, and regulatory compliance. They manage budgets, timelines, resources, vendors, and staff involved in the clinical trial, and also handle data management and reporting. They are also responsible for protocol development, site management, and monitoring the study's progress by coordinating with the clinical research associates.
Key skills for a Clinical Trial Manager include strong leadership, project management, and communication abilities. They should also be proficient in medical terminology and have a strong understanding of Good Clinical Practices (GCP), as well as FDA and ICH regulations. A degree in life sciences, nursing or related field, certification like Certified Clinical Research Professional (CCRP) or Certified Clinical Data Manager (CCDM) are often required. Prior roles before becoming a Clinical Trial Manager might include Clinical Research Associate, Clinical Data Coordinator, or Clinical Project Coordinator.
Clinical Trial Manager I US - Remote Clinical Operations Yes Regular Part-Time 2458 Overview Job Posting Title US Remote/Rockville/Frederick Emmes Group: Building a better future for us all....
Remote WorkCommunicates with the Institutional Review Board (IRB) and other departmental review committees. b. Acts as a consultant to members of the health care team. c....
Onsite Senior Project Manager- EPCM Capital Delivery Program - Life Sciences
- Rockville, MD
- 8 days ago
- Rockville, MD
- 8 days ago
Remarkable people, trusted by clients to design and advance the world. Wood is recruiting for a Senior Project Manager - EPCM Capital Delivery Program to join its Life Sciences business. This...
and implementation of FDA regulations/ICH/GCP guidelines, is required Global study execution and experience with various health and ethics agencies....
trial Assist in investigator selection, which includes documenting the qualifications and experience of the investigator with, at a minimum, the curriculum vitae, current Good Clinical Practices and...
Project Manager - Life Sciences Bioqual Inc. Rockville Post Date : Feb 21, 2025 0 6 : Job Detail Offered Salary 0 Commitment Full Time Compensation Paid Required education level Bachelor's degree...
Responsible for preparing study-related documentation such as protocol worksheets, adverse event reports, institutional review board documents, and annual continuing review reports....
Required to enter study and/or research participant data into the Clinical Trial Management System (CTMS) as applicable....
Piper Health & Sciences is looking to identify a Project Manager/Senior with expected travel between Rockville, Frederick, and Gaithersburg, MD. This role manages project delivery and portfolio...
Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens Experience with CRIO (Clinical Trial Management System...
Responsible for preparing study-related documentation such as protocol worksheets, adverse event reports, institutional review board documents, and annual continuing review reports....
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Salary for Clinical Trial Manager Jobs in Maryland
Required or preferred licenses and certifications for Clinical Trial Manager positions.
Highest Education Level
Clinical Trial Managers in Maryland offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Trial Manager position
- Budgets
- ICH GCP
- Institutional Review Board
- Clinical Trial Management System
- Study Management
- Clinical Monitoring
- Biomarkers
- Clinical Data Management
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Cancer Research
- Medical Affairs
- Scientific Research
- Drug Development
- Site Management
- Biology
- Immunology
- Clinical Trials
- Neuroscience
- Biotechnology
- Clinical Operations
- Clinical Research
- Oncology
- FDA Regulations
- Medical Device Sales
- Public Health
- Data Collection
- Patient Care
- Standard Operating Procedures
- Data Management
- Phlebotomy
- Health Care
- Medical Terminology
- Affirmative Action
- Collections
- Military Background
- Investigation
- Auditing
- Presentation
- Written Communication
- Documentation
- Collaboration
- Data Entry
- Bachelor's Degree
- Reporting
- Education Experience
- Regulations
- Policy Development
- Project Management
- Research Skills
- Microsoft Office
- Microsoft Excel
- Problem Solving
- Time Management
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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