Clinical Contracts Strategist

hace 1 semana

Madrid, Madrid, España Caidya A tiempo completo
Job Overview:

The Clinical Contracts Strategist will oversee the cross-functional execution of Clinical Contracts to ensure consistency and quality while identifying and solving any issues that potentially would delay the negotiation and execution of site contracts. The Lead directly supports the study Project Manager by collaboration with Clinical Trial Regulatory Manager (CTRM), Study Startup Lead (SSUL), and assigned personnel from the start-up functional areas: Site Contracts, Site Budgets, Feasibility, and Country Specialists.

Key Responsibilities:
  • Act as the Clinical Contracts Lead for the assigned countries and regions participating directly at kick-off meetings, sponsor calls providing the client with procedural and legal guidance, and study updates and advice as how to expedite and facilitate site contract execution.
  • Prepare the forecast of all Clinical Contract intermediate steps and oversees the execution in order to achieve contractual milestones.
  • Manage the Contracts Specialists appointed to the project and ensure they are included and granted access to all applicable study-specific systems including appropriate Egnyte folder, D365, eTMF, and study startup system accesses.
  • Accountable for creation of all study-specific contract templates within assigned countries of oversight, through either direct drafting of templates or collaboration with assigned Contract Specialists.
  • Work directly with Project Manager and Sponsor to develop cohesive contract negotiation guidelines and parameters, escalation pathways, and establishment of Sponsor-specific signature requirements as applicable.
  • Work directly with Project Manager, Grants Administration, Sponsor, and local Country Experts (including Contracts Specialists as applicable) to develop country-specific site budget templates, negotiation benchmarks, and escalation and fair market value assessment procedures and pathways.
  • Responsible for accurate forecasting of site contract execution dates and communicating timelines to key stakeholders to ensure timely activation of study sites, including oversight of site contracts and budget status entries into study startup tracking systems and external trackers.
  • Collaborate with Contracts Specialists to resolve negotiation impasses with site contracts and budgets, including direct contract and budget negotiation with study sites when appropriate.
  • Conduct fair market value assessments of budget items that fall outside of negotiation benchmarks and as applicable to facilitate Sponsor approval or provide direct approval when authorized.
  • Serve as internal point of escalation to facilitate resolution of legal language negotiations, including approval of contract terms when authorized.
  • Responsible for maintaining and updating country-specific contract templates in assigned countries of oversight within the Clinical Contracts CTA template repository.
  • Supports the development and creation of contracts related departmental intelligence tools.
  • Serves as mentor to fellow Clinical Contracts team members to assist in departmental outstanding of complex contracts issues.
  • Serves as contracts-related subject matter expert within the department and in a cross-departmental capacity.
  • May be called upon to conduct trainings.
Requirements:
  • Education: BA/BS degree in a related field, an advanced degree is preferred. Legal education background preferred (Paralegal certification or Juris Doctor).
  • Experience: Clinical research, contracts, or related experience that includes working in a team-oriented environment preferred. Minimum of three years of contracts related experience is essential and experience in a CRO or pharma setting is strongly preferred.
  • Skills/Competencies: Proficient in general and regionally-specific contract fundamentals; successfully applies this knowledge to contract drafting, review, negotiation, and amendment processes. Ability to handle multiple tasks to meet deadlines in a dynamic environment. Good understanding of clinical trial process across Phases II-IV and ICH GCP. Ability to interact effectively and appropriately with investigative site personnel. Excellent organizational skills and attention to detail, with proven ability to handle multiple tasks effectively. Analytical: be able to identify and understand site contract and budget issues in an early phase for the clinical trial and concisely convey the issue to the internal and client project team as well as draft a response to resolve the issue understanding the urgency. Ability to problem solve and work independently using own initiative. Sound judgment: displays willingness to make decisions, exhibits sound and accurate judgment, and makes timely decisions. Planning/Organizing – Prioritizes and plans work activities, uses time efficiently, and develops realistic action plans. Demonstrates flexibility and willingness to learn new skills that are relevant to the position.
  • Capabilities: Windows; proficient in MS Word, Excel, Powerpoint. Experience in industry benchmarking tools such as GrantPlan or GrantsManager is an advantage. Excellent organizational skills. Exceptional English written and oral communication skills, proficiency in other languages is an advantage. Excellent personal interaction skills.

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