Clinical Contracts Specialist

Job type:
on-site
Start:
ASAP
Duration:
12 months +
From:
Juice Resource Solutions Limited
Place:
Yorkshire
Date:
09/09/2017
Country:
flag_no United Kingdom
project ID:
1414269

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This project is archived and not active any more.
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Clinical/Pharmaceutical Contracts Specialist
Global Pharmaceutical Company
Location: Leeds
Rate: Up to GBP 37per hour or GBP 273 per day
ASAP Start

OVERVIEW:

Responsible for drafting and implementing clinical research contracts.
Responsible for monitoring and evaluating compliance with contractual requirements for all clinical investigations.
Act as the contract liaison between Johnson & Johnson Medical Devices and the investigation site or vendor, answering any questions related to the contract, resolving issues as appropriate, and working with the attorneys and internal clients as necessary.
Tracks and oversees clinical investigator contracts status, including payments, and drive effective contracting process. Audits and evaluates all clinical consulting and research agreements for compliance.
Insures compliance with all Health Care Compliance requirements as it relates to all clinical consulting and research agreements.
Communicates Healthcare Compliance requirements to clinical business consultants, Investigators and Institutions.
Support Clinical Trial Leaders within the clinical studies.

KEY JOB ACTIVITIES:

* Initiate, supervise and track status of entire contracting process for all clinical business consulting and clinical research agreements.
* Maintain agreement templates as appropriate
* Work with legal and HCC to draft and modify clinical consulting agreement and Clinical Trial Contracts.
* Develop and maintain an accurate accounting of contracts, studies, financial agreements, and contractual compliance.
* Maintain database of clinical study, business consulting and confidentiality contracts.
* Communicate with clinical consultants and Investigators regarding Healthcare Compliance requirements.
* Assist in providing internal communication of important contract status, changes in contract requirements/regulations and events.
* Ability to understand and discuss legal and financial issues for clinical research contracts.
* Coordinate with clinical project managers/leaders and site monitors for contract concerns/issues.
* Support the implementation of new clinical systems/processes.
* May be involved in other tasks to support Clinical Operations and Operating Company as needed.
* Perform all job duties in full accordance with the Worldwide Policies on Information Asset Protection, maintain password(s) as Confidential, and protect Critical Business Information.
* Incumbent knows, understands, incorporates and complies with all applicable laws and regulations relating to the company's business activities and Policies and Procedures of the Health Care Compliance Program and Code of Conduct.

SKILLS/EXPERIENCE REQUIRED:

* BS/BA in Biological Science and/or Law or MBA is preferred
* Typically requires Bachelor's degree with or without experience.
* Requires at least 2 years of previous experience in negotiating, drafting, revising and implementing contracts.
* Previous clinical research and legal experience: a plus.
* Requires experience and proficient knowledge working with computer systems (Microsoft office: Excel, Word and Powerpoint).

Due to the high volume of applications we receive we are not able to get back to everyone who applies. Therefore if you have not heard back from Juice Resource Solutions within 7 days please assume that your application has been unsuccessful however we will contact you if suitable roles come up that match your skill set.