Medical Affairs and Translational Research (MATR) Partnership Lead
Raritan, NJ - USA
Job Summary
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at
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:
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 Oncology
The 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 projects
Works 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 improvements
Partners 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 frameworks
Liaises with medical affairs Global Review Committee administrator(s) GMAL and translational science lead with respect to new IIS reviews and coordination
Advances 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&Js 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 collaboration
Qualifications
A minimum of a masters 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 preferred
Broad knowledge of disease predictive and diagnostic biomarkers related scientific methodologies and analytic techniques is required
Strong skills in collaboration and building relationships without formal authority are needed to meet MATR objectives
Critical thinking and strong communication skills are required
Project management skills and strong organizational skills are required
Comfort with ambiguity and rapidly changing scientific environment(s) is needed
Experience with principal investigators and/or as research staff involving biomarker analyses is beneficial
Experience as an industry medical liaison including oncology translational research responsibilities is desirable
Four or more years of relevant work experience in biopharmaceutical industry is preferred
Approximately 10% domestic or international travel is required
This position is based in Raritan NJ and follows a hybrid work schedule with in-house
The anticipated base pay range for this position is $122000 - $212000.
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 corporations performance over a calendar/performance year. Bonuses are awarded at the Companys 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 Companys consolidated retirement plan (pension) and savings plan (401(k)).
This position is eligible to participate in the Companys long-term incentive program.
Employees are eligible for the following time off benefits:
Vacation up to 120 hours per calendar year
Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington up to 56 hours per calendar year
Holiday pay including Floating Holidays up to 13 days per calendar year of Work Personal and Family Time - up to 40 hours per calendar year
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 :
$137000.00 - $235750.00Additional Description for Pay Transparency:
About Company
About Johnson & Johnson A t Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress. That’s why for more than 130 years, we have aimed to keep people well at every age and every stage of life. Today, as the world’s larges ... View more