[Innovative Medicine] Site Contract Manager

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 jnj.com .

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

R&D Operations

Job Sub Function:

Clinical Trial Project Management

Job Category:

Professional

All Job Posting Locations:

Seoul, Korea, Republic of

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 https://www.jnj.com/innovative-medicine

We are searching for the best talent for Site Contract Manager.

Position Summary:

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.

Principal Responsibilities:

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.

rovide 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.

Principal Relationships:

This position reports to Manager, Site Contracting

Internal :

Internal Business Partners (CCS, TA, MAF, MAO, GD, HCC, Risk Management, Legal, etc.) outside parties

External :

Clinical Investigator Sites, Commercial Suppliers, Clinical Research Organizations (when applicable).

Education and Experience Requirements:

Bachelor’s degree in appropriate scientific or business disciplines

3 experience and/or equivalent competencies in pharmaceutical industry/clinical research

Demonstrated AI literacy and an AI enabled mindset, including the ability to apply AI tools responsibly in daily work to improve productivity, decision making and quality of outcomes.

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.

Other:

Fluency in English required.

Travel Percentage: 10%

#LI-Hybrid

 

Legal Entity

Innovative Medicine

 

Job Type

Regular

Application Documents

Free-form resume AND cover letter is required (in English).

Application Deadline

Open until the position is filled.

Notes

Preference will be given to individuals subject to national veterans’ benefits and persons with disabilities upon submission of relevant documents as per applicable laws.

Only candidates who pass the resume screening will be notified individually. However, notifications may be delayed due to company circumstances.

If any false information is found in the application documents, the hiring may be canceled even after the offer is confirmed, and future applications may be restricted.

Submitted documents will not be returned and will be deleted upon request.

Required Skills:

Preferred Skills:

Analytical Reasoning, Analytics Dashboards, Business Behavior, Clinical Data Management, Clinical Research and Regulations, Clinical Trial Designs, Clinical Trials, Execution Focus, Laboratory Operations, Medical Knowledge, Process Oriented, Professional Ethics, Project Integration Management, Project Management, Research and Development, Research Ethics, Training Administration