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Regulatory and Medical Affairs - Medical Policy Advisor; Medical Research

Job in Elizabeth, Union County, New Jersey, 07215, USA
Listing for: TechDigital Group
Full Time position
Listed on 2026-09-17
Job specializations:
  • Business
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 90000 - 120000 USD Yearly USD 90000.00 120000.00 YEAR
Job Description & How to Apply Below
Position: Regulatory and Medical Affairs - Medical Policy Advisor (Medical Research)

Position Summary

The Medical Policy Advisor is a trusted and agile matrix partner who provides guidance on medical activities anchored on quality and compliance, ethics and integrity for the benefit of our patients. The Medical Policy Advisor is a member of the Medical Policy team within the Global Medical Excellence organization. This team plays a critical role to advance best practices in global medical activities through policy and governance, guidance and risk assessment, and monitoring.

Key Responsibilities
  • Provides subject matter expertise regarding medical research including scientific collaborations and partnerships aligned to related external guidelines and requirements.
  • Evaluates processes and/or procedural documents for improvement and implementation of practical solutions.
  • Interprets procedural documents, processes, and documentation requirements as well as external regulations and standards to provide consultation and advice to stakeholders while ensuring matrix alignment and consistency.
  • Partners in the development and implementation of appropriate processes, process improvements, and procedural documents in alignment with Client policies and external guidelines.
  • Writes and/or contributes to the review and revisions of policies and procedures.
Qualifications & Experience
  • College degree with a minimum of 3 years‑experience in the pharmaceutical or related industry (e.g., healthcare, research).
  • Demonstrated experience in post‑marketing medical affairs GxP activities (e.g., research, medical education) and related regulations, standards, and business requirements.
  • Familiarity with healthcare compliance and financial reporting (e.g., Sunshine Act).
  • Experience in writing procedural documents and leading process improvements.
  • Excellent organizational, written and oral communication, facilitation, interpersonal and leadership skills.
  • Ability to facilitate discussions and decision‑making with cross‑functional and cross‑cultural team members; ability to influence without authority and negotiate appropriate solutions and proven ability to establish strong internal and external stakeholder relationships.
  • Ability to clearly communicate policies and rationale to diverse audience and to present training to cross‑functional global colleagues.
  • Track record of success in leading complex projects and problem solving. Demonstrated strong project management, analytical, and critical thinking skills.
  • Change management and process improvement experience highly desired.
  • Experience working with third‑party vendors.

Physical presence at the Client worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well‑being and engagement, and it enhances the Company culture.

Top Skills
  • Demonstrated experience in post‑marketing medical affairs GxP activities (e.g., research, medical education) and related regulations, standards, and business requirements.
  • Familiarity with healthcare compliance and financial reporting (e.g., Sunshine Act).
  • Experience writing procedural documents and leading process improvements.
  • Ability to clearly communicate policies and rationale to diverse audience and to present training to cross‑functional global colleagues.
  • Track record of success in leading complex projects and problem solving. Demonstrated strong project management, analytical, and critical thinking skills.
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