About the Role

Culmen International, LLC is hiring a Clinical Protocol Developer to assist the Naval Medical Center in Portsmouth, VA. 

 

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 protocol in accordance with written policies and procedures as set forth in Title 21 of the Code of Federal Regulations, NMCP and Bureau of Medicine & Surgery (BUMED) instructions

 

This position is onsite in Portsmouth, VA. 

 

What You’ll Do in Your New Role

• Assist physicians/scientists in developing, writing, and producing human and animal research protocols in support of the military medicine research programs 

• Assist with the preparation of investigator-initiated trials to include coordination of the protocol submission, submission of amendments and regulatory compliance reports, and the development of presentations and/or publications 

• Assist with preparing informed consent statements and other study-related research documents 

• Conduct literature reviews and draft scientific and technical documents 

• Contribute to the preparation and modification of internal study budgets 

• Assist with ensuring PI-initiated protocols contain quality research design, and meet DOD standards for ethics and compliance 

• Assist the PI with addressing Scientific Review Committee (SRC), Institutional Review Board (IRB), and other committee queries 

• Attend and assist with the planning of committee meetings for disease-specific working groups to facilitate research development 

• Assist with administering the study development tracking system and updating protocol details and development events in eIRB system 

• 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 questions 

• Assist the clinical research coordinators in the development of specimen submission.  

• Assist the research and statistical data coordinators, database developers, and database administrators in study database development and data monitoring planning 

• Assist with collecting information on reported problems regarding consistency and/or clarity in open protocols. 

• Assist with initial and follow-on updates of study registration on clinicaltrials.gov, including facilitation of Quality Assurance (QA)  

• Participate in the collection of data, supporting both human and animal protocols. 

• Provide education and training to researchers and staff on protocol development  

Required Qualifications

• Bachelor's Degree
• 5 Years of Clinical Research Experience
• Ability to obtain a Secret Clearance

 

• Exceptional Medical/Dental/Vision Insurance, premiums for employees are 100% paid by Culmen, and dependent coverage is available at a nominal rate (including same or opposite sex domestic partners) 

• 401k – Vested immediately and 4% match
• Life insurance and disability paid by the company
• Supplemental Insurance Available
• Opportunities for Training and Continuing Education
• 12 Paid Holidays

  

To learn more about Culmen International, please visit www.culmen.com