Site Contract Manager

Johnson & Johnson Co.; États-Unis; À distance; USD 90 000 - 130 000; Plein temps

Résumé du poste

Johnson & Johnson is seeking an Associate Site Contract Manager for a remote role across the United States. You will prepare, negotiate, and finalize clinical trial agreements and budgets, overseeing sites or CROs, while ensuring compliance and cost control.

Responsibilities include contract lifecycle management, confidentiality agreements, and collaboration with QA, auditors, and the global CCS team to mitigate risk and drive efficiency.

Qualifications

• Bachelor's degree with 3+ years experience in pharmaceutical industry/clinical research; must understand clinical development process
• 2+ years' experience with negotiation and contracts
• Demonstrated AI literacy and an AI-enabled mindset to improve productivity and outcomes
• Familiarity with healthcare compliance guidance (HIPAA, FCPA, Safe Harbor) a plus
• Familiarity with clinical research processes
• Ability to work effectively in cross-functional teams
• Strong negotiation and problem resolution skills
• Working knowledge of PCs (MS Office at a minimum) and database management

Responsabilités

• Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company-sponsored and/or investigator-initiated studies
• Provide support for negotiations in confidentiality agreements, informed consent forms and other documents
• Participate in budget development for site/investigator costs aligned with fair market value
• Manage the contract amendment lifecycle and related metrics tracking
• Review and authorize site payments ensuring compliance with study costs
• Assist QA/auditors and provide process improvement recommendations
• Collaborate with global CCS team to analyze terms and assess risks
• Support overall contract execution to drive efficiency and savings

Connaissances

Contract negotiation

Budget management

Cross-functional collaboration

AI literacy

Negotiation and problem resolution

Healthcare compliance knowledge

Teamwork in virtual environments

Formation

Bachelor's degree

Outils

MS Office

Contract management software

Databases

Description du poste

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

Titusville, New Jersey, United States of America

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

This is a remote role available in all states within the United States of America. While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application.

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

Purpose: The Associate 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. They will provide support to the clinical team in the pricing, planning, execution and control of site/investigator budgets and contracts.

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 with 3+ years experience and/or equivalent competencies in pharmaceutical industry/clinical research; must have a working knowledge of the clinical development process
• 2+ years' experience with negotiation and contracts
• 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
• 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.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran stat