Senior Product Management Support I

Job Description

Overview
Please note that this position is contingent upon the successful award of a contract currently under bid.

Goldbelt Apex, a part of the Healthcare Technology Transformation Group, is a data-focused company dedicated to process and quality in every aspect. As experts in healthcare IT experts, Apex is committed to building systems for healthcare organizations to seamlessly communicate and exchange data across different systems and devices.

Summary:
Goldbelt APEX is looking for a Senior Product Management Support I.

Responsibilities
Essential Job Functions:
Support product/project management of therapeutics, prophylactics, diagnostics, investigational products, and clinical protocols.
Develop/review regulatory documentation.
Coordinate FDA/IRB activities.
Participate in and lead IPTs/working groups.
Support IND product accountability, protocol management, technical reports, training, and stakeholder coordination.

Qualifications
Necessary Skills and Knowledge:
Medical product development.
FDA-regulated products and clinical programs.
IND protocols.
Regulatory documentation.
Clinical project/program management.
Cross-functional stakeholder coordination.
Minimum Qualifications:
Ability to understand and apply cGCP, cGLP, and cGMP.
Knowledge of FDA requirements and Title 21 CFR applicable to IND protocols.
Knowledge of DoD acquisition, Force Health Protection, and clinical/FDA-regulatory product development.
Travel: Up to 20%
Preferred Qualifications:
Current FHP incumbent.
DHA Office of Regulated Activities experience.
IND product/protocol management experience.
IRB interaction/approval experience.
Military medical countermeasure experience.
CONUS/OCONUS operational support experience.

Pay and Benefits
The annual salary for this position is $95,000 to $125,000.

At Goldbelt, we value and reward our team's dedication and hard work. We provide a competitive base salary commensurate with your qualifications and experience. As an employee, you'll enjoy a comprehensive benefits package, including medical, dental, and vision insurance, a 401(k) plan with company matching, tax-deferred savings options, supplementary benefits, paid time off, and professional development opportunities.

Essential Job Functions:
Support product/project management of therapeutics, prophylactics, diagnostics, investigational products, and clinical protocols.
Develop/review regulatory documentation.
Coordinate FDA/IRB activities.
Participate in and lead IPTs/working groups.
Support IND product accountability, protocol management, technical reports, training, and stakeholder coordination.

Requirements

Necessary Skills and Knowledge:
Medical product development.
FDA-regulated products and clinical programs.
IND protocols.
Regulatory documentation.
Clinical project/program management.
Cross-functional stakeholder coordination.
Minimum Qualifications:
Ability to understand and apply cGCP, cGLP, and cGMP.
Knowledge of FDA requirements and Title 21 CFR applicable to IND protocols.
Knowledge of DoD acquisition, Force Health Protection, and clinical/FDA-regulatory product development.
Travel: Up to 20%
Preferred Qualifications:
Current FHP incumbent.
DHA Office of Regulated Activities experience.
IND product/protocol management experience.
IRB interaction/approval experience.
Military medical countermeasure experience.
CONUS/OCONUS operational support experience.

Pay and Benefits
The annual salary for this position is $95,000 to $125,000.

At Goldbelt, we value and reward our team's dedication and hard work. We provide a competitive base salary commensurate with your qualifications and experience. As an employee, you'll enjoy a comprehensive benefits package, including medical, dental, and vision insurance, a 401(k) plan with company matching, tax-deferred savings options, supplementary benefits, paid time off, and professional development opportunities.