<img height="1" width="1" alt="" style="display:none" src="https://www.facebook.com/tr?id=785769564843890&ev=PixelInitialized" />
Screen shot 2015 06 26 at 3.54.23 pm.jpg
Search for Jobs by David Wright

Home-based Pharmaceutical Sr. Contracts Analyst, Clinical Site Agreements  (Science & Biotech)
Durham, NC 27703
Recruited by: David Wright | Recruiter | DOCS See all my Jobs

  • Hiring Company: DOCS
  • Industry: Science & Biotech
  • Compensation: Salary: 85K to 115K
  • Expires: Jan 02, 2020
Share this job:
Please ensure all fields are filled in and your resume is attached


Submit your information and resume instantly with Monster!

Job Description


Responsible for the development and analysis of contractual relationships which includes but is not limited to drafting, negotiating, and finalizing contracts and grants related to clinical trials. Assists in and/or directs the development of scope of work and analysis of terms and conditions. Provides specialized support to trial managers and clinical group in the pricing, planning, execution and control of grants and contracts

Principal Responsibilities:

• Responsible for drafting, negotiating, and finalizing clinical trial agreements with sites as they relate to various clinical projects.
• Draft master investigator grants globally according to the R&D grant pricing guidelines, and based on adequate scope of work, clinical trial protocol and other clinical trial information.
• May be asked to establish agreement templates with frequently used sites.
• Determine potential needs for contract amendments and manage amendment execution.
• Analyze clinical trial agreements and identify areas of concern and/or contention prior to obtaining formal legal counsel advice.
• Assure that contractual terms and provisions are in compliance with corporate process, systems, and strategies.
• Act as liaison to legal counsel to resolve contractual/legal issues with sites.
• Assume responsibility for all aspects of document and metrics tracking.
• Review, authorize and/or manage payments in an accurate and timely fashion.
• Assist clinical operations or clinical team in ensuring that investigator grants comply with overall study costs.
• Adhere to SOPs, ethics and departmental compliance as determined by management as well as R&D companies, corporate, HCC and QA guidelines.
• Contribute to improving processes and establish refinements that reduce cycle time, create savings and improve efficiency in the initiation of clinical trial sites.
• Collaborate with other members of the Contracts and Grants team and contract consultants to ensure proper dissemination and management of knowledge and to meet team goals and objectives.
• Comply with requests from QA and auditors.
• This is not an exhaustive, comprehensive listing of job functions. Other duties may be performed as assigned

Education: Bachelor’s degree in appropriate scientific or business disciplines.

Necessary Experience:

• Several years negotiating clinical trial agreements and clinical contracts
• Excellent written and oral communication skills.
• Knowledge of Microsoft Office applications especially Excel.
• Good interpersonal skills demonstrated as energetic, proactive, enthusiastic, and independent thinker.
• Ability to negotiate and obtain commitment and buy-in from customers, suppliers and team members.
• Ability to collaborate and build strong partnership/relationships with all functions involved in the trial
• Excellent organizational skills.

DOCS is the FSP division of ICON Clinical Research. We provide global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical development industry.

DOCS is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.