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Medical Lead

Location: High Wycombe, Buckinghamshire Salary: £100 - £120 per hour
Sector: Pharmaceuticals Specialism:
Type: Contract Contact: Matt Henocq

Medical Lead

  • Directs the operational function in medical affairs to achieve organizational objectives.
  • Responsible for the design, development and implementation of programs related to educational, promotional and reporting materials for products related to Phase IIIb, Phase IV trials, solicited and non-solicited studies, publications, and so on.
  • At this level, the position has a greater degree of impact on the business results and typically, responsibility for managing a group of professionals
  • Manages the design and implementation plans of medical affairs program, including identification of critical paths, budget development and tracking of all projects.
  • Manages and delegates work of direct reports.
  • Establishes accountability for assignments.
  • Manages creation of educational, promotional and reporting materials for use by internal stakeholders.
  • Manages publication planning, preparation and review.
  • Supports technical training needs of partners.
  • Manages review of promotional material. Implements plans for clinical trials, including protocol, staffing and budgeting as it relates to business initiatives.
  • Ensures that trials/registries are conducted according to all applicable guidelines, regulations, company procedures and high ethical/quality standards.
  • Implements policies and procedures for development and provision of medical and technical information pertaining to the company's products for internal use by customer and by government.
  • Manages budget, contract negotiation and oversight of vendor activities.
  • Executes the company's drug surveillance/product safety program which includes following up on adverse reaction reports.
  • Provides solutions surrounding legal liability and compliance with government.
  • Maintains collaborative working relationship between medical affairs and internal stakeholders to deliver timely and expert support to product development.
  • Must be a final signatory as per ABPI Code of Practice

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