Caidya
Job Description:
Job Overview:
The Contracts Manager (CM) 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. CM acts as Contract Lead (CL) in a project and 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. The CL provides Clinical Contracts strategy, and expertise to deliver timely negotiation of site contracts and budgets and to ensure accurate forecasts of contract execution timelines to support cross functional coordination and delivery of site activations. The strategy will reflect the CL’s prior site contract and budget experience and technical knowledge of contract negotiations, budget fair market value practices, applicable legal theories and regulations including GDPR, and administrative requirements of participating study sites and countries.
Job Duties and Responsibilities:
Supervisory Responsibilities:
No supervisory responsibilities.
Job Requirements:
+ BA/BS degree in related field, with an advance degree preferred
+ Legal education background preferred (Paralegal certification or Juris Doctor)
+ Clinical research, contracts, or related experience that includes working in a team-oriented environment preferred
+ Minimum of 3 years of contracts related experience is essential and experience in a CRO or pharma setting is strongly preferred
+ Excellent understanding of contracting principles and requirements
+ Familiar with budget development, benchmarking practices, and fair market value principles is required
+ 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
+ Windows; proficient in MS Word, Excel, Power point. 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 language is an advantage
+ Excellent personal interaction skills