Site Contracts Specialist - Anywhere US

Company
Synteract
Location
United States
Salary
Competitive
Posted
22 Jan 2021
Closes
21 Feb 2021
Ref
28930
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
Site Contracts Specialist - Anywhere, US

Remote

Who We Are

Synteract ® , a Syneos Health ® company, is a leading full service Contract Research Organization (CRO) with a successful three-decade track record of supporting emerging biotech and pharmaceutical companies. With our mission of Bringing clinical trials to life TM , we provide customized Phase I through IV services globally, offering expertise across multiple therapeutic areas, including notable depth in oncology, dermatology, general medicine, infectious disease and vaccine, neuroscience, pediatrics, and rare and orphan diseases.

Position Overview

As a Site Contracts Specialist you are responsible for ensuring contract management skills are applied to all negotiated site contract types such that contractual, financial and legal goals are met. Identifies and ensures contractual risks are minimized. Provides support and input for resolving significant contractual issues and, if needed, ensures timely elevation to Executive Management and/or legal counsel.

Specific tasks would include:
  • Serves as a contracting resource for internal and external customers.
  • Supports Site Contracting activities: prepares and negotiates contractual agreements and budgets.
  • Provides support and input for elevating any potentially controversial or unfavorable language to the Sponsor or internally as appropriate for preliminary review.
  • Prepare and manage the negotiations of Site Contracts as assigned:
    • Primary contact for clinical sites and liaison between client and clinical sites for the negotiation of site contract documents.
    • Manages and facilitates the timely negotiation of site contractual documents in accordance with project specific timelines; anticipates and identifies potential issues and communicates to the Project Manager to prevent delay of project deliverables; targets and suggests alternative solutions and assists with the creation and implementation of a remedial action plan to facilitate the administration and timely completion of the site contractual documents.
    • Collects, verifies and provides accounting with the I.R.S. forms required for payment, e.g., W-9 and/or Foreign Vendor Certification.
    • Participate in internal and external project team meetings, if required.
    • Responsible for tracking the amount of time budgeted for and spent on site contract document negotiation; communicate all out-of-scope activities or over scope time to Project Management.
    • Tracks progress of contract document negotiation in tracking tool.
    • Provides instructions to accounting and project team to have clinical site set up in clinical trial and accounting systems.
  • Maintains correspondence, positive relations and interaction with internal and external customers.
  • Reviews relevant site contract policies and procedures and provides input to management.
  • Identifies issues associated with departmental processes, provide recommendations and assist with the implementation of corrective actions.
  • Executes special projects as needed to assist internal customers.
  • Takes leadership role for resolving significant contractual issues and, if needed, ensures timely elevation to Executive Management and/or legal counsel.

Qualifications
  • Bachelor's degree or equivalent in a life science, business, accounting or related field of study and a minimum of 5+ years related experience or equivalent combination of education and experience.
  • Minimum of 2 years of CRO or legal contracts experience is needed.

Specific Knowledge
  • Understanding of the clinical process (Phase I - IV) and the ramifications of change to one or more study assumptions, including timelines.
  • Advanced knowledge of the practices, procedures, and processes involved in contract administration.
  • Advanced knowledge of relevant laws, FDA regulations, corporate terms, conditions and policies governing assigned contracts.
  • Intermediate proficiency in Microsoft Word, MS Project, Excel, and PowerPoint, Outlook.
  • Effective verbal and writing skills; English + local language, if relevant.

This job excludes Colorado applicants.

If you're passionate about bringing clinical trials to life, we encourage you to apply today!

Synteract's policy is to provide equal employment opportunity and affirmative action in all of its employment practices without regard to race, color, religion, sex, national origin, ancestry, marital status, protected veteran status, age, individuals with disabilities, sexual orientation or gender identity or expression or any other legally protected category. Applicants for positions with Synteract must be legally authorized to work in the country which they are applying and verification of employment eligibility will be required as a condition of hire. The Company will not sponsor applicants [to this position] for work visas.

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