Growing and well-respected biomedical (clinical, basic and applied) research firm has openings at Ft. Detrick. If you are passionate about research, and are looking for a firm that shares your passion, and provides competitive salaries with a strong benefits package, join the ClinicalRM team.
We are currently seeking a Scientist III for the Frederick, MD area.
The offeror shall provide scientific oversight and technical knowledge in the areas of bioengineering, biology, chemistry, and vaccine development. The offeror shall support and analyze the development of medical technologies, including, but not limited to, the following:
Developing, overseeing, and reviewing proposals, protocols, and study designs to support nonclinical (i.e., immunogenicity, toxicity, and efficacy) and clinical testing, assay development, and manufacturing efforts
Assessing technology readiness levels
Ensuring test protocols conform with FDA requirements
The offeror shall author and edit documents, reports, and briefings; interpret technical data, specifications, and requirements; and assist in development of risk management efforts. Additionally, the offeror shall work closely with the product team to solve problems and ensure application of appropriate scientific principles to meet technical requirements.
Maintain a safe workplace ensuring that he/she is aware of and observes appropriate safety and occupational health rules and regulations. Employee is required to attend safety training relative to his/her position and report any infractions of safety procedures to the facility Safety Officer.
Performs light duties and other related duties as required and assigned.
Education: Successful completion of a full course of study in an accredited college or university leading to a Master’s Degree, preferably with a major in Engineering, Systems Management, Business Management, or a related discipline, is required. DAU Level III certification in PM, SPRDE, or the civilian equivalent, is preferred. A combination of a Bachelor’s Degree, DAU Level III certification in PM or SPRDE, and eight (8) years of experience may be substituted for a Master’s Degree.
General Experience: Eight (8) years of general experience, four (4) years of experience in a program office or similar organization, and one (1) year of experience in a program management position
Specialized Knowledge and Skills: May lead technical working groups to support product development and monitor Industry to identify innovative technologies applicable to program goals. Experience with product development, production, and storage; development of vaccines through FDA licensure; animal model development; and CBD bio-surveillance is required.
Must be able to work independently following a brief period of specific technical training.
Qualified candidates will receive consideration for employment without regard to race, color, religion, sex, or national origin. Candidates for positions under ClinicalRM’s contracts with the Department of Defense (DoD) will be required to pass one or more background/security investigations conducted by the DoD, U.S. Army, or other Federal Government agency. Such investigations may include criminal records and credit history checks.
ClinicalRM is an Affirmative Action-Equal Opportunity Employer
“NorthCoast 99” Best Places to Work recipient
ClinicalRM is a Contract Research Organization supporting government and commercial clinical research for biologics, drugs, and devices.