USA - Medical Reviewer - III - USD

Pfizer; Cambridge (MA); Hybrid; USD 137,760 - 155,668; Part time

Benefits offered by this job

Comprehensive Benefits Package

Short-Term Disability (STD)

Long-Term Disability (LTD)

Supplemental and Voluntary Life Insurance

Job summary

A leading pharmaceutical company in Cambridge, MA is seeking a Medical Reviewer to ensure promotional and non-promotional materials meet regulatory standards. The role requires a degree in a scientific or healthcare-related field and ideally AQP certification with 5-7 years of experience. You will collaborate with cross-functional teams, provide compliance guidance, and review materials in accordance with the ABPI Code of Practice, ensuring effective use of medicines and stakeholder engagement.

Qualifications

• Certification as an Appropriately Qualified Professional (AQP) preferred.
• Proven experience in reviewing promotional and non-promotional materials.
• Ability to interpret scientific data for content development.

Responsibilities

• Review and approve materials according to the ABPI Code of Practice.
• Provide scientific input during the content development process.
• Collaborate with teams to support content creation and regulatory submissions.
• Manage compliance strategies and intercompany communication.

Skills

Degree in a scientific or healthcare-related field

AQP Certification

5-7 years experience

Strong understanding of the ABPI Code of Practice

Effective communication

High attention to detail

Strong organizational skills

Education

Degree in a scientific or healthcare-related field

Job description

USA - Medical Reviewer - III - USD (Contract)

Cambridge, MA, United States (Hybrid)

Contract (1 year 1 day)

Published 1 day ago

AQP Certification

Promotional & Non - Promotional Material Review

Clinical Content

Medical Content

stakeholder communication

Advisory Support

Medical Legal Regulatory

ABPI Code of Practice

Regulatory Compliance

Summary

The main function of a Medical Reviewer is to ensure that promotional and non-promotional materials comply with regulatory standards and internal policies. This role provides scientific and Code of Practice expertise, supporting the development and approval of content that enables the appropriate use of medicines and effective stakeholder engagement.

Job Responsibilities

Review and approve materials in line with the ABPI Code of Practice, acting as the Appropriately Qualified Professional (AQP) where applicable.

Provide scientific input and compliance guidance during the development of promotional and non-promotional content.

Collaborate with cross-functional teams to support content creation, training materials, and regulatory submissions.

Contribute to the development of compliance strategies and manage complaints or intercompany dialogue when required

Skills

Degree in a scientific or healthcare-related field.

Certification as an Appropriately Qualified Professional (AQP) preferred. 5-7 years experience required.

Strong understanding of the ABPI Code of Practice and regulatory frameworks.

Ability to interpret scientific data and apply it to content development.

Effective communication and collaboration across cross-functional teams.

High attention to detail and strong organizational skills.

Additional Locations

Pearl River, NY and Collegeville, PA

Pay Rate Range

Min Pay Rate $100

Max Pay Rate $113

Currency USD

Unit hourly

Benefits Information

Comprehensive Benefits Package available based on eligibility

Short-Term Disability (STD)

Long-Term Disability (LTD)

Supplemental and Voluntary Life Insurance