30 Sep
Pricing and Contract Strategy Manager With Pharmaceutical/Clinical
Delaware, Wilmington , 19850 Wilmington USA

Vacancy expired!

PRICING AND CONTRACT STRATEGY MANAGER WITH PHARMACEUTICAL/CLINICAL WILMINGTON, DE Local to Wilmington: HYBRID (3 days Onsite/2 days Remote). Possibility for FTE Conversion Project Description:

  • Study Contract Manager (SCM) play an important role in driving the costings and contracts being responsible for negotiation and budgeting in clinical trials and for developing and managing contracts and annexes with investigators and institutions or external vendors ensuring ethical, fair, and compliant practices.
  • SCM has regular communication with investigators and institutions as well as other key external and internal stakeholders.
  • SCM might have different internal titles based on the experience level .
  • The experience level depends on the years of experience, performance record, level of independence in the role, ability to take on additional tasks or tutor more junior colleagues.
  • The Director, Country Head may assign this internal title after confirmation with Senior Director, Cluster Head or Executive Director, Regional Head).
  • Adapt global templates of agreements to local use in accordance with local requirements and SOPs.
  • Develop and negotiate clinical site budgets based on Fair Market Value.
  • Negotiate agreement language and budget with clinical study sites.
  • Act as point of contact and interface with Legal if necessary to ensure integrity of contracts.
  • For each agreement maintain the status of agreement, budgets, issues, payments, any amendments for the duration of the study, and communications with internal and external sources .
  • Ensure final contract documents are consistent with agreements reached at negotiations.
  • Ensure all agreements are executed in a timely manner contributing to efficient site start-up timelines.
  • Support internal and external audit activities.
  • Ensure compliance with company's Code of Conduct and company policies and procedures relating to people, finance, technology, and security.
  • Ensure that all contracts are included in the TMF .
  • Training and mentoring of new members of the local Study Team regarding financial/contractual issues and sharing experiences.
  • Support preparation and negotiation of a Local Master Service Agreement .
  • Contribute to process improvements, knowledge transfer and best practice sharing.
Required Skills:
  • Bachelor's degree in related discipline, preferably in life science, law, finance or equivalent qualification.
  • Excellent knowledge of international guidelines ICH-Google Cloud Platform, basic knowledge of GMP/GDP.
  • Good knowledge of relevant local regulations.
  • Basic understanding of the drug development process.
  • Good understanding of Clinical Study Management including monitoring, study drug handling and data management.
  • Excellent attention to details.
  • Good written and verbal communication skills.
  • Good collaboration and interpersonal skills.
  • Good negotiation skills.
  • Ability to work in an environment of remote collaborators.
  • Post-graduate training in contracts administration or work experience as a paralegal in pharmaceutical or health care industry.
  • Manages change with a positive approach for self, team, and the business.
  • Sees change as an opportunity to improve performance and add value to the business.
  • Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time.
  • Good analytical and problem-solving skills.
  • Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines.
  • Familiar with risk-based monitoring approach including remote monitoring.
  • Good cultural awareness.
  • Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an enabled environment.
  • Team oriented and flexible; ability respond quickly to stakeholders .
This 9+month position starts ASAP. Please E-MAIL your resume (attachment to email) with rate and availability to Bridget: ALPHA'S REQUIREMENT #22-02707 MUST BE ELIGIBLE TO WORK IN THE U.S. AS AN HOURLY W2 EMPLOYEE

Vacancy expired!


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