Medical & Technical Advisor for Clinical Trials

Bering-Alaka'ina Holdings, LLC; Frederick (MD); On-site; USD 120,000 - 180,000; Full time

Benefits offered by this job

401K with company match

Medical, dental, disability and life保险

Tuition reimbursement

Paid time off

11 paid holidays

Job summary

Bering-Alaka`ina Holdings, LLC is seeking a Medical and Technical Advisor Support Specialist to support government activities in Frederick, MD at Fort Detrick. The role covers clinical trial planning, regulatory affairs, and medical device development across DoD projects.

The candidate will work with IPTs, develop trial protocols, and ensure FDA/DoD compliance while coordinating with stakeholders to align research strategies and product development plans.

Qualifications

• Must hold medical or scientific/technical degree.
• 6–8 years of relevant experience in medical product development or clinical trials.
• Expertise across medical devices, diagnostics, drugs/biologics, and other medical countermeasures.
• Experience with site selection, recruitment, and regulatory processes (FDA/DoD).

Responsibilities

• Provide expertise in medical devices, diagnostics, drugs/biologics, and other medical countermeasures.
• Clinical management expertise for DoD-sponsored and non-DoD research activities.
• Plan, design, coordinate, manage, and conduct clinical trial research protocols.
• Assist in writing clinical protocols and trial documents; serve as a key IPT member.
• Develop research strategy for clinical trials and site assessments.
• Coordinate regulatory strategy with DoD and FDA guidance documents.

Skills

Medical devices expertise

Diagnostics/medical countermeasures

Clinical trial planning

Regulatory affairs (FDA/DoD)

CMC knowledge

Site recruitment/retention

IPT participation

GMP compliance

Technical writing

Education

Medical degree or doctorate or related advanced degree

Job description

Bering-Alaka`ina Holdings, LLC is seeking a Medical and Technical Advisor Support Specialist to support government activities in Frederick, MD at Fort Detrick. The role covers clinical trial planning, regulatory affairs, and medical device development across DoD projects.

The candidate will work with IPTs, develop trial protocols, and ensure FDA/DoD compliance while coordinating with stakeholders to align research strategies and product development plans.