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Medical Information Contractor II

Advanced Clinical·Salary not specified

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Job description

About the Position

Medical Information Contractor II

Code: 36007

Posted: 2026-04-13

Type: Contract

Remote: Yes

Salary Range: $0 Per Hour

Category: Medical Affairs


We are seeking a detail-oriented and proactive Medical Information Contractor to support the delivery of accurate, compliant, and timely medical information. This role plays a critical part in ensuring regulatory adherence while serving as a trusted resource for healthcare professionals and internal stakeholders.


Responsibilities

  • Ensure all medical, ethical, and legal responsibilities related to product and device information are handled in accordance with regulatory and compliance standards
  • Identify and appropriately escalate product quality complaints, adverse events, and safety information in alignment with regulatory guidelines and internal procedures
  • Receive, document, and respond to written medical information inquiries from healthcare professionals and internal teams
  • Develop and maintain medical response materials, including standard response documents (SRDs), FAQs, and communication templates
  • Serve as a subject matter resource by providing product and process education to internal and external stakeholders
  • Conduct quality reviews of medical information cases and call documentation to ensure accuracy and compliance with safety and reporting standards
  • Provide feedback, corrections, and retraining support to team members when needed to maintain service quality
  • Collaborate cross-functionally on projects and contribute to the delivery of scientific and technical product information
  • Support onboarding, training, and ongoing development of medical information and contact center team members
  • Manage and resolve escalated cases requiring higher-level medical review

Requirements

  • Pharmacist (PharmD or RPh required)
  • Minimum of 1+ year of experience in pharmaceutical or biotechnology medical information
  • Strong understanding of regulatory requirements related to:
    • Medical information
    • Pharmacovigilance (PV) / adverse event (AE) reporting
    • Product quality complaints (PQC)
  • Excellent written, verbal, and interpersonal communication skills
  • Ability to work independently in a fast-paced, high-demand environment
  • Strong organizational skills with a proactive mindset and sense of urgency
  • Comfortable collaborating across cross-functional teams
  • Proficient in Microsoft Office (Word, Excel, PowerPoint), Outlook, and Microsoft Teams

We Offer

  • Competitive salary
  • Remote work options
  • Health coverage, life insurance, disability insurance, and 401k benefits

About the Company

At Advanced Group, our commitment to diversity and inclusion in every part of our organization is crucial to fulfilling our mission and demonstrating our REAL values. Advanced Group is committed to providing employment opportunities without regard to sex, race, color, age, national origin, religion, gender identity or expression, sexual orientation or sexual preference, pregnancy or maternity, genetic information, marital status, disability, veteran status, or any other basis protected by applicable federal, state or local law.

Advanced Group complies with federal and state disability laws and makes reasonable accommodations for applicants and candidates with disabilities. If a reasonable accommodation is needed to participate in the job application or interview process, please contact [email protected].

© Advanced Clinical. This job description was sourced from the employer's public career page. TheJob is not the employer — we index the posting and route candidates to the source. All content rights and hiring decisions belong to the employer.

Advanced Clinical is a global clinical development organization that provides CRO, FSP, Quality & Validation, and Strategic Resourcing services for biopharmaceutical and medical device organizations. Our mission is to deliver a better clinical experience for our clients. With global experience in over 50 countries, we are committed to improving all lives touched by clinical research. We understand the complex nature of the clinical research industry and approach each opportunity with compassion. Together, we answer the hopes of patients and healthcare professionals with industry-leading services in global life-sciences.

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