About the Role
Culmen International, LLC is hiring a Clinical Protocol Developerย to assist the Naval Medical Center in Portsmouth, VA.ย
This position will support the Department Head of CID and is accountable for research related matters to the PIs of each research protocol. Provide support to the Department Head of CID and the PI of each protocolย in accordance withย written policies and procedures asย set forth inย Title 21 of the Code of Federal Regulations, NMCP and Bureau of Medicine & Surgery (BUMED) instructions
This position is onsite in Portsmouth, VA.ย
What You'll Do in Your New Role
- Assistย physicians/scientists in developing, writing, and producing human and animal research protocols in support of theย military medicine research programsย
- Assistย with the preparation of investigator-initiated trialsย to includeย coordination of theย protocolย submission, submission of amendments and regulatory compliance reports, and the development of presentationsย and/or publicationsย
- Assistย with preparing informed consent statements and other study-related research documentsย
- Conduct literature reviews and draft scientific and technical documentsย
- Contribute to the preparation and modification of internal study budgetsย
- Assistย with ensuring PI-initiated protocolsย containย quality research design, and meet DOD standards for ethics and complianceย
- Assist the PI with addressing Scientific Review Committee (SRC), Institutional Review Board (IRB), and other committee queriesย
- Attend andย assistย with the planning of committee meetings for disease-specific working groups toย facilitateย research developmentย
- Assistย with administering the study development tracking system and updating protocol details and development events inย eIRBย systemย
- Work with the data management team, clinical operations team, and other research collaborators in transitioning projects from the development team to the operations team that incorporates the clinical details needed to treat patients and the research elements to answer study questionsย
- Assistย the clinical research coordinatorsย in the development of specimen submission.ย ย
- Assistย the research and statistical data coordinators, database developers, and database administrators in study database development and data monitoring planningย
- Assistย with collecting information on reported problemsย regardingย consistency and/or clarity in open protocols.ย
- Assistย withย initialย and follow-on updates of study registration on clinicaltrials.gov, including facilitation of Quality Assurance (QA)ย ย
- Participate in the collection of data, supporting both human and animal protocols.ย
- Provide education and training to researchers and staff on protocol developmentย ย
Required Qualifications
- Bachelor's Degree
- 5 Years of Clinical Research Experience
- Ability to obtain a Secret Clearance
About the Company
Culmen International is committed to enhancing international safety and security, strengthening homeland defense, advancing humanitarian missions, and optimizing government operations. With experience in over 150 countries, Culmen supports our clients to accomplish critical missions in challenging environments.
To learn more about Culmen International, please visit www.culmen.com
At Culmen International, we are committed to creating and sustaining a workplace that upholds the principles of Equal Employment Opportunity (EEO). We believe in the importance of fair treatment and equal access to opportunities for all employees and applicants.ย Our commitment to these principles is unwavering across all our operations worldwide.
The determination of compensation at Culmen International, LLC is based on various factors such as location, the individual's unique combination of education, knowledge, skills, competencies, clearance level, experience, internal equity, contract-specific affordability, and organizational requirements.ย
Employment Type: FULL_TIME