Medical Advisor – DoD Clinical Trials Specialist

International Executive Service Corps; Frederick (MD); On-site; USD 95,000 - 130,000; Full time

Job summary

Bering-Alaka`ina Holdings, LLC is seeking a Medical Advisor Support Specialist to provide expert support for a government customer at Fort Detrick, MD. The role focuses on medical devices, diagnostics, drugs, and biologics, with responsibilities spanning clinical trial design, regulatory strategy, and site management.

The candidate will lead regulatory planning, contribute to trial protocols, and coordinate with DoD and DHA stakeholders to ensure compliance and successful trial execution.

Qualifications

• Must hold a medical degree, doctorate, or related advanced degree in medical, scientific, or technical field.
• Minimum of four (4) years’ relevant experience in medical product development or clinical trials.
• Experience with medical devices, diagnostics, drugs, biologics, or countermeasures.
• Knowledge of clinical trial strategy, site selection, and regulatory considerations.

Responsibilities

• Provide expertise in medical devices, diagnostics, drugs, biologics, and countermeasures.
• Offer clinical management support for DoD- and non-DoD-sponsored trials.
• Develop contract management plans and design clinical protocols.
• Assist in writing and preparing clinical protocols and trial documents.
• Advise on site selection, training, recruitment, and retention.
• Coordinate regulatory strategy per DoD and DHA regulations.
• Review safety data, trial documents, and regulatory submissions.
• Participate in IPT meetings and site visits.

Skills

Medical devices

Diagnostics

Drugs & biologics

PTSD & TBI

Clinical trial planning

Site recruitment

CMC knowledge

Regulatory affairs

DoD acquisition

Education

Medical degree or related advanced degree

Job description

Bering-Alaka`ina Holdings, LLC is seeking a Medical Advisor Support Specialist to provide expert support for a government customer at Fort Detrick, MD. The role focuses on medical devices, diagnostics, drugs, and biologics, with responsibilities spanning clinical trial design, regulatory strategy, and site management.

The candidate will lead regulatory planning, contribute to trial protocols, and coordinate with DoD and DHA stakeholders to ensure compliance and successful trial execution.