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Mgr, Clinical Vendor and Site Contracts

Evolution Research Group
Posted 2 months ago, valid for 9 days
Salary

$85,000 - $95,000 per year

Contract type

Full Time

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Sonic Summary

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  • The Manager of Clinical Vendor and Site Contracts at a CRO is a remote position requiring a minimum of 5 years of clinical contracting and budgeting experience.
  • The role involves negotiating contracts, managing vendor relationships, and coordinating vendor management activities for clinical projects.
  • Candidates should have strong analytical, negotiation, and communication skills, along with proficiency in Microsoft Excel.
  • The position also requires experience in drafting and reviewing legal terms, budgets, and contracts, with a preference for clinical research experience.
  • Salary details are not provided in the job description.

Job Title: Manager of Clinical Vendor and Site Contracts, CRO

Location: Remote 

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following.  Other duties may be assigned.  Employee performs all, part, and/or any combination of the duties listed below.

  • Main point of contact and represent Company in vendor relationships.
  • Negotiate scope of work, product pricing, and contracts with vendors per various clinical projects
  • Liaise with Company Business Development team to obtain proposals from vendors in alignment with Sponsor’s RFP scope and timelines 
  • Develop and implement vendor selection programs, preferred partnerships, and volume discounts
  • Liaise with vendor, Company project team, and Sponsor
  • Coordinate vendor management activities and processes
  • Suggest vendor management processes, policies, and methods
  • Track, review, and approve vendor invoices
  • Reconcile vendor budget s
  • Amend, renew, and close out vendor contracts 
  • Maintain internal vendor archiving and documentation
  • Update contract terms of existing vendors
  • Liaise with Company Business Development team to estimate investigator grants for Sponsor RFPs based on adequate scope of work, clinical trial protocol and other clinical trial information
  • Draft, negotiate, and finalize site contracts and amendments for various awarded clinical projects
  • Draft, negotiate, and finalize site budgets and amendments for various awarded clinical projects
  • Track institutional costs and legal language for contracts across multiple sites per industry FMV
  • Track, review, and approve site invoices
  • Communicate and work effectively with clinical sites regarding pricing (including vendor pricing), patient stipends, advertising, enrollment, study start dates, etc.) and legal terms via email and phone.
  • Establish master service agreements, as necessary.
  • Develop and negotiate rate cards for MSAs, as necessary.

QUALIFICATIONS

  • Previous work experience with drafting, reviewing, and negotiating legal terms including MSAs, work order, POs, amendments, etc.
  • Previous work experience executing contracts and document signatures
  • Previous work experience drafting, reviewing, and negotiate unit costs and total budgets
  • Previous work experience with vendors /third parties 
  • Clinical Research experience preferred
  • Reading and understanding vendor scope from protocol/RFP
  • Previous work experience with creating budgets   and estimating costs without a pricing tool system.
  • Experience with subject procedures and site fees.

EDUCATION and/or EXPERIENCE

Bachelor’s degree or equivalent and 5+ years of clinical contracting and budgeting experience

SKILLS and/or ABILITIES

  • Strong analytical skills and ability to extrapolate budget calculations. 
  • Strong skills and working knowledge in Microsoft Excel
  • Strong negotiation skills
  • Excellent time management and organizational skills
  • Excellent communication and interpersonal skills
  • Detail oriented and ability to QC/find errors. 
  • Quick decision making and problem-solving skills.
  • Ability to set timelines and adhere to turnaround times.
  • Ability to offer improved customer service.





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