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Clinical Trial Education and Literature Review Specialist

Remote:

Full Remote

Contract:

Fixed term

Experience:

Mid-level (2-5 years)

Work from:

Canada

Offer summary

Qualifications:

Bachelor’s degree in life sciences or related field, 2-4 years in clinical research or medical affairs, Experience with Promotional Review Committees, Strong understanding of regulatory requirements.

Key responsabilities:

Develop and submit clinical trial education materials for PRC approval
Conduct literature reviews on new medical indications and trends
Collaborate with cross-functional teams on educational material alignment
Monitor industry trends impacting clinical trial materials
Synthesize complex information into clear educational content

ICONMA Human Resources, Staffing & Recruiting Large https://www.iconma.com/

1001 - 5000 Employees

See more ICONMA offers

Job description

Clinical Trial Education and Literature Review Specialist

Location: Remote
Duration: 7- 8 Months

Description:
We are seeking a detail-oriented and analytical Clinical Trial Education and Literature Review Specialist to support the development and submission of clinical trial education materials to the Promotional Review Committee (PRC). This role is also responsible for conducting comprehensive literature reviews to assess the landscape of new and emerging medical indications. The ideal candidate will work closely with cross-functional teams, including medical affairs, regulatory, and marketing, to ensure that all materials are accurate, compliant, and aligned with the latest medical research.

Key Responsibilities:
Develop, organize, and submit clinical trial education materials to the Promotional Review Committee (PRC) for review and approval, ensuring compliance with regulatory and company guidelines.
Provide ongoing support during the PRC review process, addressing feedback, revising materials, and ensuring timely approval.
Conduct thorough literature reviews to gather and analyze data on new medical indications, treatment trends, and advancements in the field.
Collaborate with cross-functional teams (Clinical Development, Medical Affairs, Regulatory, Marketing, etc.) to ensure educational materials align with clinical trial objectives and reflect the latest medical information.
Monitor and stay current on industry trends, new therapies, and scientific advancements that may impact clinical trial materials or strategic positioning.
Synthesize complex medical and scientific information into clear, concise educational content for internal and external audiences.
Assist in the development of communication strategies that effectively educate healthcare professionals about clinical trials, investigational products, and new medical indications.
Ensure all educational materials are updated and consistent with the latest clinical trial data and regulatory requirements.
Maintain a comprehensive database of clinical trial education materials and literature review findings for easy access and future reference.

Qualifications:
Bachelor’s degree in life sciences, clinical research, healthcare, or a related field (Advanced degree preferred).
2-4 years of experience in clinical research, medical affairs, regulatory affairs, or medical communications.
Experience preparing materials for Promotional Review Committees or similar review bodies.
Strong understanding of clinical trial processes, regulatory requirements, and promotional guidelines (e.g., FDA, EMA).
Demonstrated experience conducting literature reviews, including the ability to analyze,

As an equal opportunity employer, ICONMA provides an employment environment that supports and encourages the abilities of all persons without regard to race, color, religion, gender, sexual orientation, gender identity or express, ethnicity, national origin, age, disability status, political affiliation, genetics, marital status, protected veteran status, or any other characteristic protected by federal, state, or local laws.