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Clinical Scientific Liaison - 615587

5+ years
$130K
10 Nov. 27, 2024
Job Description
Job Type: Full Time Education: M.Sc/PhD/MD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Opportunity: Clinical Development & Medical Affairs Professional
Location: Flexible (depending on client needs)


Job Summary:

We are seeking a Clinical Development professional with experience in Medical Affairs to join a biopharmaceutical company. In this role, you will be responsible for understanding and discussing clinical trial design, working with physicians on clinical trial parameters (e.g., inclusion/exclusion criteria, regulatory aspects), and managing various aspects of the clinical development process. Your responsibilities will also include working with Key Opinion Leaders (KOLs), supporting investigator boards, preparing slide decks for meetings, and occasional site visits when needed. Please note, this is not a sales role.


Key Responsibilities:

  • Clinical Trial Design: Collaborate with cross-functional teams to design clinical trials, with a focus on trial protocols, patient selection (inclusion/exclusion criteria), and regulatory aspects.
  • Medical Affairs Collaboration: Work closely with the Chief Medical Officer (CMO) and other stakeholders to manage clinical development activities, including the creation and review of investigator brochures, study documents, and other clinical materials.
  • Engagement with KOLs: Interact with KOLs and external experts, facilitating productive discussions and keeping them informed about the clinical program.
  • Regulatory Support: Provide guidance on regulatory requirements and ensure compliance with clinical trial regulations and guidelines.
  • Slide Deck Creation: Prepare and manage slide decks for internal and external presentations, ensuring scientific and clinical accuracy.
  • Investigator Board Management: Support and manage investigator boards, helping to organize meetings, discussions, and information sharing.
  • Occasional Site Visits: Conduct site visits as required to ensure smooth study operations, address site issues, and provide clinical trial support.

Requirements:

  • Education: MSc, PhD, or MD in a relevant field.
  • Experience:
    • 5+ years of experience in clinical development or a related role within the pharmaceutical or biopharmaceutical industry.
    • Strong understanding of clinical trial design, regulatory requirements, and clinical development processes.
    • Oncology experience is essential; radiopharmaceutical experience is a plus but not required.
  • Skills:
    • Strong knowledge of clinical trial regulations and Good Clinical Practice (GCP).
    • Experience working with KOLs and managing clinical development activities.
    • Ability to prepare and present slide decks for clinical and regulatory meetings.
    • Strong communication and interpersonal skills, with the ability to collaborate effectively with internal and external teams.

Why Apply?

  • Impactful Role: Play a crucial role in advancing clinical development within a leading biopharmaceutical company.
  • Scientific and Professional Growth: Work closely with KOLs, physicians, and industry experts while gaining exposure to innovative oncology and radiopharmaceutical developments.
  • Collaborative Environment: Work with a dynamic team that values collaboration and scientific excellence.

This position offers a chance to grow within the clinical development field while contributing to cutting-edge research in oncology and beyond.

For more information or to apply, please reach out to the recruitment team.