Clinical Site Contract Specialist - Saha Sözleşme Uzmanı

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:
R&D Operations

Job Sub Function:
Clinical Trial Support

Job Category:
Professional

All Job Posting Locations:
Istanbul, Turkey

Job Description:

Johnson & Johnson Innovative Medicine is recruiting for a Clinical Site Contract Specialist to be based in İstanbul / TURKIYE.

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.

Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

You will be responsible for:


* Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and/or investigator-initiated studies through direct negotiation with clinical trial sites or via oversite of a Clinical Research Organization responsible for contract negotiations.


* Provide support for negotiations in confidentiality agreements, informed consent forms and other ancillary contract documents as required.


* Participate in discussions related to the development of site/investigator budgets aligned with fair market value.


* Manage the contract amendment lifecycle.


* Assume responsibility for all aspects of legal document and metrics tracking.


* Provide support to review, authorize and/or understand aspects of site payments.

Assist clinical operations or clinical team in ensuring that investigator grants comply with overall study costs and compliance guidelines.


* Comply with requests from QA and auditors.


* Work proactively to provide recommendations to improve processes and establish refinements that reduce cycle time, create savings, and improve efficiency in the initiation of clinical trial sites.


* Work with the global CCS team as necessary to review and analyze contractual terms to reach resolution.

Assess risks of budget and legal provisions in conjunction with members of the CCS team and support functions.

Escalate issues as appropriate.


* Exemplary customer focus with vision to drive solutions.


* This is not an exhaustive, comprehensive listing of job functions.

Other duties may be performed as assigned.

Qualifications / Requirements:


* Bachelor’s degree in appropriate scient...