Search Jobs

Senior Contracts Manager

Edison-New Brunswick Metro Area, NJ

Posted: 07/26/2019 Job Type: Scientific Job Number: JN -072019-25277
PRIMARY JOB RESPONSIBILITIES:
1. Clinical Trial Agreement (CTA) Management.
  • Develop CTA per patient budgets using Grant Manager.
  • Draft study specific CTA templates.
  • Finalize CTA templates and per patient budgets with study teams.
  • Negotiate and establish pre-approval and approval workflows; review roles, task timelines and responsibilities; and negotiation parameters with study teams.
  • Draft, negotiate, and execute site specific CTAs within established study timelines and study budgets.
  • Develop, draft, and negotiate CTA amendments within established study budgets.
  • Assist with managing the Data Driven Payment process for assigned studies.
  • Lead and coordinate CTA management for large studies.
  • Lead and coordinate CTA management for all studies within a project.
2. Draft, negotiate, and execute contracts and contract amendments for company and Pharmacology studies.
3. Ensure contracts are executed within fair market standards as appropriate.
4. Answer questions and resolve problems concerning all assigned studies and individual contracts.
5. Track workflow and contract cost for all assigned studies and individual contracts.

ADDITIONAL JOB RESPONSIBILITIES:
1. Engage in process improvement initiatives both inside and outside the Contracts Management Group (CMG).
2. Provide some mentoring to junior associates within the CMG.
3. Assist with developing and maintaining CMG procedures for contract management as needed.
4. Support developing processes, standard templates, and quality definitions and metrics as appropriate.

POSITION QUALIFICATIONS:
Education:
  • BA/BS Degree
  • Experience:
  • 3-5 years of experience creating, negotiating and executing contracts in a pharmaceutical or biotech company or Contract Research Organization (CRO).
Licensure/Credentials:
  • None
Knowledge, Skills, and Abilities:
  • Knowledge of the pre-clinical, clinical, and periapproval drug development process required.
  • Advanced skills in Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft Access
  • Experience using Adobe Acrobat Professional and Microsoft Office SharePoint.
  • Proficiency with specialized industry databases such as GrantPlan/Grants Manager a plus.
Must possess excellent skill/ability in the following:
  • Project Management
  • Time Management
  • Conflict Resolution
  • Dealing with Difficult People
  • Written Communication
  • Organizing
  • Initiative
  • Decision Making
  • Problem Solving
  • Oral Communication
  • Team Building
  • Influencing Others
  • People Relationships
  • Accountability
  • Judgment


Apply Online

Send an email reminder to:

Share This Job:

Related Jobs:

Login to save this search and get notified of similar positions.