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Clinical Operations Manager III

Company CAMRIS International, LLC
Job Location Bethesda, MD
Salary Range $60–$80k
Time Type Full Time
Seniority Senior Level
Posted January 26, 2026
Application Deadline February 10, 2026

Overview:

We are seeking a Clinical Operations Manager III to support the National Institutes of Health’s (NIH), world renowned National Institute of Allergy and Infectious Diseases (NIAID) in Bethesda, MD. Our NIAID professional, technical, and scientific support personnel are part of a preeminent team focused on positively impacting millions of lives around the world with groundbreaking research. Candidates will work at a prominent and vibrant NIAID worksite to directly support exciting ongoing research activities as a contractor team member. Accelerate your career and apply below to help us make a difference.

CAMRIS International is a dynamic clinical research and international development firm that achieves innovative solutions to health and development challenges through high-quality, cost-effective programs and research management services. We combine our proven systems with today’s most effective, evidence-based best practices. Our core practice areas include: clinical research; vaccine research, microbiology and infectious disease research, development and production; biodefense; global health security; and HIV/AIDS programs.

Our employees enjoy a collegial environment where individual contributions matter at all levels. At CAMRIS, you will notably improve the lives of people at home and abroad.

Responsibilities:

  • Manage the oversight of sponsor essential documents/ records files for multi-center studies and electronic trial master files.
  • Advance the writing of documents as part of the quality management system (SOPs, policies, audit reports, etc.), by both actively leading the development of documents and facilitating working groups to collaborate and write documents.
  • Stay current with changes to current industry standards and applicable regulations for quality in clinical research.
  • Conduct quality assurance activities such as internal audits, reviews of regulatory documents, drafting summary reports for division leadership, and others as assigned.
  • Participate in preparations for regulatory inspections, which may include reviewing inspection readiness plans, mock inspections, and risk-based management of program inspection quality events.
  • Assist in resolving compliance issues at clinical sites, clinical vendors, and contracted research facilities; and provide assessment of the impact of any deficiencies.
  • Provide guidance to other groups in DMID that are funding, overseeing, and implementing clinical research to understand how clinical research is supported by DMID.
  • Based on understanding of Division operations, look for ways to standardize processes to improve quality and/or facilitate efficiency.
  • Performs other duties as assigned.

Qualifications:

  • Bachelor’s degree in a related discipline.
  • Minimum of three (3) years of experience in clinical research or a related field.
  • Thorough knowledge of clinical trial documentation including Essential Documents/Records according to ICH.
  • Must be detail-oriented with strong organizational skills.
  • Experience with US and international Good Clinical Practice (GCP), guidance documents, and industry best practice in all areas of a GxP environment.
  • Extensive experience with electronic trial master file systems and electronic data capture.
  • Experience in regulatory inspections from the US FDA or similar government regulatory authorities is preferred.
  • Experience conducting or overseeing audits is preferred.
  • Experience working at a clinical research site or overseeing multicenter clinical research is preferred.
  • Experience in the NIH or other government agency is preferred.
  • Excellent communication skills both verbally and written; and across functions internally and externally.
  • Ability to organize, prioritize and deliver tasks & projects according to pre-defined deliverables.
  • Ability to effectively build and maintain relationships with multiple departments and external entities (e.g., Investigator sites, clinical Vendors/CROs) in order to effectively solve problems.
  • Excellent multi-tasking, analytical, organizational and teamwork skills.
  • Ability to troubleshoot, identify root causes, and systematically resolve problems.
  • Ability to produce high-quality work on complex problems with cross-functional involvement.
  • Proficient in Window based software to include Excel, Word.

Physical Requirements:

The physical requirements described here are representative of those that must be met by a candidate to perform the essential functions of this job. Reasonable accommodations may be provided to enable individuals with disabilities to perform essential job functions.

  • Constantly will be required to perform sedentary work that primarily involves sitting/standing.
  • Occasionally will be required to perform light work that includes moving objects up to 20 pounds.
  • Occasionally will be required to push or pull less than 25 pounds, and use both hands.
  • Constantly will be required to have clear vision (near and/or far), depth perception, peripheral vision, and/or visual acuity.
  • Occasionally will be required to move about to accomplish tasks or move from one worksite to another.
  • Constantly will be required to communicate with others to exchange information.
  • Constantly will be required to assess the accuracy, neatness, and thoroughness of the work assigned.
  • Regularly works in an environment free from adverse environmental conditions.

Please submit your resume online at *www.CAMRIS.com*. CAMRIS is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran status, disability status, or any other characteristic protected by any applicable federal, state, or local law.

CAMRIS offers a comprehensive benefits package, including medical, dental, and vision insurance for individuals and families, FSAs, HSA, life and AD&D insurance, short- and long-term disability, legal services, voluntary hospital indemnity, critical illness and accident insurances, EAP, pet insurance, 401(k) with employer match and Roth option, tuition and professional reimbursement, public transportation support in the DMV area, a referral bonus program, vacation with tenure-based increases, PTO, 11 paid holidays, paid bonding leave, and paid supplemental short-term disability.

Employment is contingent upon successful completion of a Public Trust-level background check, a requirement for this position under an active federal contract. The background check process may include, but is not limited to the following: (1) contacting your professional references; (2) verification of previous employment, education and credentials; (3) a criminal background check; (4) use/abuse of federally-controlled substances; and (5) a department of motor vehicle check. Candidates must be prepared to fully-complete any required background check questionnaire during initial onboarding.