Medical Affairs and Translational Research (MATR) Partnership Lead

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.comAs 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: Medical Affairs GroupJob Sub Function: Medical AffairsJob Category:Scientific/TechnologyAll Job Posting Locations:Raritan, New Jersey, United States of AmericaJob Description:Medical Affairs and Translational Research (MATR) Partnership Lead for J&J OncologyThe MATR Partnership Lead is a key point of contact for medical affairs (regional and global) and translational research for preclinical investigator-initiated study (IIS) proposals, collaborative studies or MAF-funded company-sponsored studies involving key biomarker objectives. The individual will link internal strategic and tactical workstream(s) supporting research proposal reviews and final decisions for key studies. MATR partnerships will also include line-of-sight to data read-outs or draft publication timelines for contracted studies to support knowledge exchange between translational research, external research community, clinical and medical affairs.Tasks for this position include the following:Provides subject matter expertise, execution, and process leadership for medical affairs and translational science, preclinical or biomarker research projectsWorks closely with disease area leads on triaging biomarker or preclinical IIS proposals from external researchers or non-clinical collaborative study requests from concept-to-execution.Supports key internal and external stakeholder communications, preclinical review agendas and review decisions. Leads efforts to capture process metrics & analytics to recommend and implement iterative process improvementsPartners with oncology translational research lead(s) in preparing biomarker and preclinical “one-pager” strategy for inclusion in worldwide medical affairs evidence generation plans and IIS strategic frameworksLiaises with medical affairs Global Review Committee administrator(s), GMAL and translational science lead with respect to new IIS reviews and coordinationAdvances global medical affairs company-sponsored study concepts with key biomarker objectives through internal governance reviews where applicable with Global Head, Evidence Generation and Oncology Translational Research Review Forum (OTRRF)Ensures research discussions, submission and internal reviews of preclinical/biomarker IISs or collaborative research proposals follow J&J’s Cross-Pharma Policies and SOPs.Engages with oncology translational research (OTR)’s preclinical IIS coordinator on ReCAP reviews, contracts, material transfer agreement administration to understand study statuses or interim/final data read-outs and publications. Supports global medical affairs lead(s) and global strategy & execution leads with internal knowledge exchange as required Identify and develop strategic relationships with external partners to identify opportunities for collaborationQualificationsA minimum of a master’s level degree in a life or health sciences discipline is required; Advanced scientific degree is preferred.Laboratory experience in translational research or genomics medicine is preferredBroad knowledge of disease, predictive, and diagnostic biomarkers, related scientific methodologies, and analytic techniques is requiredStrong skills in collaboration and building relationships, without formal authority, are needed to meet MATR objectives,Critical thinking and strong communication skills are requiredProject management skills and strong organizational skills are requiredComfort with ambiguity and rapidly changing scientific environment(s) is neededExperience with principal investigators and/or as research staff involving biomarker analyses is beneficialExperience as an industry medical liaison including oncology translational research responsibilities is desirableFour or more years of relevant work experience in biopharmaceutical industry is preferredApproximately 10% domestic or international travel is requiredThis position is based in Raritan NJ and follows a hybrid work schedule with in-houseThe anticipated base pay range for this position is $122,000 - $212,000.The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/performance year. Bonuses are awarded at the Company’s discretion on an individual basis.Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.Employees may be eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).This position is eligible to participate in the Company’s long-term incentive program.Employees are eligible for the following time off benefits:Vacation – up to 120 hours per calendar yearSick time - up to 40 hours per calendar year; for employees who reside in the State of Washington – up to 56 hours per calendar yearHoliday pay, including Floating Holidays – up to 13 days per calendar year of Work, Personal and Family Time - up to 40 hours per calendar yearAdditional information can be found via the following link: The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market. 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 status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please contact us via or contact AskGS to be directed to your accommodation resource.Required Skills:Preferred Skills:Analytical Reasoning, Analytics Dashboards, Clinical Research and Regulations, Clinical Trials Operations, Communication, Content Evaluation, Data Analysis, Digital Culture, Digital Literacy, Healthcare Trends, Medical Affairs, Medical Communications, Medical Compliance, Mentorship, Product Strategies, Relationship Building, Report Writing, Strategic Thinking, Tactical Planning, Technical CredibilityThe anticipated base pay range for this position is :$137,000.00 - $235,750.00Additional Description for Pay Transparency:SummaryLocation: Raritan, New Jersey, United States of AmericaType: Full time