Syneos Health

Senior Site Contracts Lead in France

Expiring today

Location
France (FR)
Salary
Competitive
Posted
23 Dec 2020
Closes
22 Jan 2021
Ref
AN/20009205
Hours
Full Time
Contract Type
Permanent
Experience Level
Management

JOB SUMMARY Manages negotiation of clinical study agreements (CTAs) on a study level and drives CTA document finalization and execution, including contractual language & terms, financial attachments, and investigator grant budgets in collaboration with a global team of site contract negotiators for Site Contracts Service Center for awarded projects. Ensures global CTA negotiation comply with sponsor and Company requirements. Identifies project and/or Company level investigator budget related problems, and works with internal and external team members to provide and implement solutions. Establishes strong working relationships with customers and internal project teams. Supports global operational initiatives at the project, Sponsor or relationship level.  May serve as strategic point of contact for internal and external customers to meet site contracting/budgeting goals. 

 

JOB RESPONSIBILITIES

 

  • Oversees negotiations of clinical study agreements (CTA´s) on a study level and drives CTA document finalization and execution, including contractual language & terms, financial attachments, and investigator grant budgets in collaboration with a global team of site contract & budget negotiators.

 

  • Provides oversight of contact & budget negotiations status and manages escalation of out-of-parameter queries on budgetary and contractual requests to sponsor decision-makers in all regions of study conduct.  Provides consultation during escalation of out-of-parameter queries as needed.

 

  • Acts as first-line subject matter expert for all such CTA elements on assigned studies for internal and sponsor stakeholders alike.  Advises stakeholders on issue resolution within the context of assigned studies.  May seek additional support from internal support structures as needed.

 

  • Plans contract execution strategy for assigned studies—including forecast of site-specific contractual execution timelines with as much accuracy as possible—and coordinates with internal study team stakeholders to ensure that CTA strategy is aligned with overall study start-up plans and expectations overall.  Manages expectations of internal and sponsor study team regarding global CTA negotiations for assigned studies.

 

  • Coordinates communications between study team stakeholders and global team of site-facing site contract & budget negotiators including roll-up of all status updates to regular team forum.  Participates in regular study calls to facilitate communication as needed.

 

  • Works closely with internal stakeholders and with Sponsor to prepare site contractual templates, including payment terms, and study-level negotiation parameters and processes within Company standards in order to drive successful negotiation of contracts and budgets.

 

  • Establishes strong working relationships and collaboration with Sponsor to ensure site contractual templates fit into the global strategy set for the program.

 

  • Creates and maintains document status reports, and updates department tools/systems and team members on a regular basis; ensures appropriate documentation is maintained.

 

  • Collaborates with internal and external legal, finance and clinical operations departments, including communicating and explaining legal and budgetary issues.

 

  • Manages site and study level discussions with internal and sponsor team stakeholders around fair market value of investigator budgets and payment terms within corporate and industry standards during negotiation with sites.

 

  • May support BU and organization through help desk and other defined pathways to resolve and deescalate issues.

 

  • Performs other work-related duties as assigned.  Minimal travel may be required (up to 25%). 

 

QUALIFICATION REQUIREMENTS

 

  • BS degree in life sciences, a health related field, or equivalent combination of education and experience.
  • Preferred experience in a CRO/pharmaceutical industry and related clinical trial expertise (Study Coordinator, CRA, Pharmacy, Nursing, Healthcare Administration) or site start-up experience.
  • Thorough knowledge of applicable regulations, drug development and clinical project management procedures.
  • Good presentation, documentation and interpersonal skills. Proficient in MS Office (Word, Excel and PowerPoint), MS Project, outlook and Internet.
  • Ability to handle multiple tasks to meet deadlines, delivering high quality work in a dynamic environment.

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