Medical Advisor Support

Systems Plus, Inc.; Frederick (MD); Hybrid; USD 130,000 - 170,000; Full time

Benefits offered by this job

Benefits package

Growth opportunities

Job summary

Systems Plus, Inc. in Frederick, Maryland seeks a Medical Advisor Support to guide medical research, regulatory strategy, and product development for DoD programs.

You will work with government leaders, clinicians, and industry partners to move scientific innovations toward fielded capabilities. The role requires at least 10 years in medical product development or clinical trials, DoD acquisition familiarity, and a strong understanding of FDA regulations, CMC, INDs.

Qualifications

• Minimum 10 years of relevant experience in medical product development/clinical trial research.
• Experience applying DoD regulatory requirements and FDA CFR/IND processes.
• Bachelor's degree in a relevant area preferred.

Responsibilities

• Provide expert guidance on medical technologies and regulatory strategy for DoD programs.
• Collaborate with DoD stakeholders, researchers, and industry partners to shape development paths.
• Prepare regulatory submissions and ensure FDA/DoD compliance.
• Review clinical protocols, safety data, and CMC considerations for product development.

Skills

Clinical research

Regulatory strategy

Medical devices/biologics

DoD regulatory knowledge

Education

Bachelor's degree in a relevant area

Job description

Got the Government Contractor Blues? Looking for a company that cares and goes beyond just filling another contract billet? Well, look no further! Experience this family-oriented company that takes pride in you and will help you grow where your passions lie. Holding many Defense & Federal government contracts around the globe, with Systems Plus, you have the opportunity to take on new and evolving challenges, aim beyond what you think you are capable of, and work in collaborative, dynamic, and high-tempo environments.

Our employees are our most valued asset, and we invest in our people because we are in it for the long term. We are committed to your success and well-being and offer competitive benefits packages, salaries, bonus/award programs, and a high potential for professional growth and job opportunities worldwide.

Systems Plus is the company for you! Experience the difference, and let's talk about your future at Systems Plus today.

Position Title

Medical Advisor Support

Position Type

Full-Time, Hybrid

Position Location

Frederick, Maryland

Tracking Code

01229

Daily Responsibilities

Join a high-impact team advancing the Department of Defense’s medical research and product-development mission. In this role, you will provide expert guidance on cutting-edge medical technologies, clinical research, regulatory strategy, and product development efforts that support Warfighters and military healthcare outcomes. Working alongside Government leaders, researchers, clinicians, and industry partners, you will help shape the path from scientific innovation to fielded medical capabilities that make a real difference in national defense and public health.

• Provide expertise in the areas of medical devices, diagnostics, drugs and biologics, and/or other medical countermeasures; and/or blood and blood products/components and other medical solutions; and/or post-traumatic stress disorder and traumatic brain injury.
• Provide clinical management expertise for both DoD- and non-DoD clinical research activities.
• Attend and participate in site visits, IPT meetings and briefings, and sub-working group and investigator meetings.
• Orchestrate the requisite regulatory strategy as well as organization and compliance activities as contained in appropriate DOD and DHA regulations, policies, pamphlets, and SOP.
• Interact with stakeholders to assist in identifying, interpreting, prioritizing, and analyzing FDA, CFR, DoD, and DHA policies, regulations, and guidance documents as they relate to products in different stages of development.
• Coordinate and assist with Joint Trauma System (JTS) to develop Clinical Practice Guideline(s) in support of the full rate decision or off-label use of the materiel solution.
• Collaborate to identify regulatory affairs (RA) strategies will optimize product development.
• Review and analyze summaries, progress reports, clinical protocols, investigator brochures, and safety profiles and safety surveillance data.
• Facilitate an understanding of requirements for compliance with all applicable FDA regulations.
• Understand and plan for future clinical trials and other pre-clinical trial milestones.
• Coordinate and assist in the review of all pre-clinical trial documents.
• Keep current files of all information disseminated by FDA and other policy bodies that affect products and interpret, synthesize, and incorporate the new information into the organization.
• Assist in the development of a comprehensive Integrated Master Plan/IMS of FDA and non-FDA regulatory and clinical activities (e.g. tasks, documents, meetings,) to include estimated timelines required to support the product development of medical devices, drugs, biologics, blood and blood products and or other medical solutions.
• Provide professional medical review of Investigational Device Exemption, IND protocols, IND packages, and plans for management of IND products.
• Provide subject matter expertise in pharmaceutical quality/chemistry, manufacturing, and controls (CMC).
• Review technical documents (e.g., Master Production Records/Batch Production Records, testing protocols/reports, investigations, Corrective and Preventive Actions, etc.) and regulatory submissions (e.g., INDs, amendments, annual reports, protocols, IBs) as requested and provide feedback to the Product Manager.
• Assess CMC related risk of commercial partners. Perform audits and GMP compliance advice.
• Be a substantive participant in IPTs as a SME.
• Provide expert written reviews, briefings, and recommendations for developmental medical projects to include reviewing and interpreting results.
• At the end of data analysis, support scientific preparation of results for eventual publication in peer reviewed scientific journals or other media or publication.
• Provide a medical/expert review of documents to be submitted to the FDA, EPA or other Governmental or Military organizations. Provide manuscript reviews for documents/reports submitted to scientific journals.

Degree and Certifications:

• Bachelor’s degree in a relevant area preferred

Required Experience:

• Minimum 10 years of relevant experience in medical product development/clinical trial research.
• Have the capability of applying knowledge of the DoD’s acquisition process in conjunction with expertise in performance of all technical advisor support tasks.

Required Clearance:

• Background investigation

About Systems Plus

Systems Plus is headquartered in Rockville, MD with over 2 decades of experience providing Global Enterprise Management, Technology, Engineering and Professional services and solutions across Defense and Federal Civilian government sectors.

From Discovery to Delivery, Systems Plus brings a greater measure of confidence, commitment and value to our clients. With various Defense and Federal contracts across the United States, Europe and Pacific/Asia, we are driving innovation and excellence within the Special Operations Forces Components and Commands, Defense Health Agency, United States Air Force, United States Marine Corps, National Institute of Standards and Technology, House of Representatives and more.

Through our diverse portfolio of clients and capabilities we power vision and insight - discover what's possible with a Small Business that thinks BIG!