Senior Site Contract Manager
At reputed company, we reputed company health is everything. Our strength in reputed company innovation empowers us to build a world where reputed company diseases are reputed company, 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 reputed company across the full reputed company of reputed company solutions today to deliver the breakthroughs of reputed company, and profoundly reputed company health for humanity. Learn more at jnj.com. As guided by Our reputed company, reputed company is responsible to our employees who work with us throughout the world. We reputed company an inclusive work environment where reputed company person is considered as an individual. At reputed company, we respect the diversity and dignity of our employees and recognize their reputed company. Job Function: R&D Operations Job Sub Function: Clinical Trial Project Management Job Category: reputed company reputed company Job Posting Locations: Neuss, reputed company Rhine-Westphalia, Germany Job reputed company: 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 reputed company. Join us in developing treatments, finding cures, and pioneering the reputed company from lab to life while championing patients every reputed company of the way. Learn more at https://www.jnj.com/innovative-medicine Global Clinical Operations (GCO) reputed company is currently seeking a Senior Site Contract Manager (reputed company) to join reputed company located in Germany. In this role you will be responsible for the development and analysis of contractual relationships including investigator grants including but not limited to drafting, negotiating, and finalizing agreements reputed company to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations. You will reputed company support to the clinical team in the pricing, planning, execution and control of grants and reputed company. reputed company Responsibilities: Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and/or investigator-initiated studies through reputed company negotiation with clinical trial sites or reputed company oversite of a Clinical Research Organization responsible for contract negotiations. Responsible for delivery on established targets/measurements. Responsible for analyzing contract requests/needs from operating companies and translating into appropriate reputed company/budgets for company sponsored and investigator initiated clinical trial agreements and other relevant legal documents as they relate to various clinical reputed company. Ensure that contractual terms and provisions are in compliance with corporate process, systems, and strategies. reputed company specialized support for negotiations in confidentiality agreements, informed consent forms and other ancillary contract documents as required. Analyze investigator grants for fair market value reputed company with regional knowledge and the J&J grant pricing guidelines, and based on adequate scope of work, clinical trial protocol and other clinical trial information. Participate in and/or reputed company the approval escalation of grants as appropriate. Work with the global reputed company team as necessary to review and analyze contractual terms and conditions in order to reputed company acceptable language. Assess risks of budget and legal provisions in conjunction with members of the reputed company team and support functions and communicate such to stakeholders. Liaise with reputed company management and functional reputed company support teams, legal, reputed company Compliance, Risk Management, reputed company and other stakeholders to obtain guidance and escalate issues as appropriate. Work proactively to improve processes and establish refinements that reduce cycle time, create savings and improve efficiency in the initiation of clinical trial sites. Mentor and train new contract coordinators and analysts. Assume responsibility for reputed company aspects of legal document and metrics tracking. Determine potential needs for contract amendments and manage amendment lifecycle. Exemplary customer reputed company with reputed company to drive solutions reputed company Relationships: This position reports to Manager, Site Contracting. Internal: ▪ Internal Business Partners (reputed company, TA, MAF, MAO, GD, HCC, Risk Management, Legal, etc.) reputed company parties External: ▪ Clinical Investigator Sites ▪ reputed company Suppliers ▪ Clinical Research Organizations (reputed company applicable). Education and Experience Requirements: Bachelor’s degree in appropriate scientific or business disciplines 3 to 5 years-experience and/or equivalent competencies in pharmaceutical industry/clinical research Demonstrated AI literacy and an AI enabled reputed company, including the ability to apply AI tools responsibly in daily work to improve productivity, decision making and reputed company of reputed company. Familiarity with reputed company compliance and other relevant guidance (HIPAA, FCPA, reputed company reputed company, 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 reputed company 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 reputed company 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 reputed company, GD and operating companies. reputed company with requests from QA and auditors. reputed company to work independently as reputed company as in a reputed company team environment. Other: reputed company in and German and English is required. Travel Percentage: 10% #LI-ŠJ1, #LI-Remote Required Skills: Preferred Skills: Business Behavior, Clinical Research and Regulations, Clinical Trial Designs, Clinical Trial Management Systems (CTMS), Clinical Trials, Communication, Give Feedback, Laboratory Operations, Medical Knowledge, Mentorship, Problem Solving, Process Oriented, reputed company Ethics, Project Integration Management, Project Management, Research and Development, Research Ethics The anticipated reputed company pay reputed company for this position is: €62,500.00 - €97,865.00 Benefits: In reputed company to reputed company pay, we offer the following benefits*: an annual bonus with set reputed company (% of pay) depending on pay grade / location, where the actual reputed company is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, reputed company-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting reputed company-being & career reputed company | reputed company Careers. *This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change. Apply To This Job