Join to apply for the Site Contract Manager role at Johnson & Johnson Innovative Medicine
Join to apply for the Site Contract Manager role at Johnson & Johnson Innovative Medicine
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 Function
R&D Operations
Job Sub Function
Clinical Trial Project Management
Job Category
Professional
All Job Posting Locations :
Job Description
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 & Johnson is currently seeking a Site Contract Manager to be located in Italy.
Site Contract Manager is responsible for preparing, negotiating, and finalizing agreements and budgets related to clinical trials and / or overseeing a Clinical Research Organization responsible for contract negotiations. Provide support to the clinical team in the pricing, planning, execution and control of site / investigator budgets and contracts.
* 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
Education And Experience Requirements
* Bachelor’s degree in appropriate scientific or business disciplines
* 3 experience and / or equivalent competencies in pharmaceutical industry / clinical research
* Familiarity with healthcare compliance and other relevant guidance (HIPAA, FCPA, Safe Harbor, etc.) a plus
* Must have a working knowledge of the clinical development process with two (2) years of negotiation and contract experience
* Familiarity with clinical research processes
* Ability to work effectively in cross function teams
* Strong and proven negotiation and problem resolution skills
* Working knowledge of PCs (MS Office suite at a minimum) and database management
* Must demonstrate innovative spirit, have strong interpersonal skills, and ability to manage a high volume of work
* Previous experience working in virtual teams preferred.
Decision-making And Problem-solving
* Adhere to SOPs, ethics and departmental compliance as determined by GD management as well as operating companies, corporate, HCC and QA guidelines. Ensure familiarity with departmental and corporate processes including but not limited to the relevant processes associated with CCS, GD and operating companies. Comply with requests from QA and auditors.
* Comply with requests from QA and auditors.
* Able to work independently as well as in a collaborative team environment.
Seniority level
Seniority level
Not Applicable
Employment type
Employment type
Full-time
Job function
Job function
Management and Manufacturing
Pharmaceutical Manufacturing
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