Medical Director, Study Responsible Physician
Not Disclosed•Full-TimeOn-site
location_onSpring House Tavern, 1032, North Bethlehem Pike, Spring House, Lower Gwynedd Township, Montgomery County, Pennsylvania, 19477, United States
About Johnson & Johnson
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.
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. We respect the diversity and dignity of our employees and recognize their merit.
Work location
Work model: On-site
Spring House Tavern, 1032, North Bethlehem Pike, Spring House, Lower Gwynedd Township, Montgomery County, Pennsylvania, 19477, United States
Lower Gwynedd Township, Pennsylvania
Key Responsibilities
- check_circleLead project scientists and provide mentoring, training, and supervision for clinical study teams
- check_circleCo-lead authorship of informed consent forms, study manuals, clinical study reports, and regulatory documents
- check_circleReview external clinical research proposals and manuscripts prepared for publication
- check_circleAct as liaison between the company and clinical investigators while building relationships with opinion leaders
- check_circleParticipate in strategic study start-up planning, feasibility assessments, and site activation
- check_circleSupport development and compilation of NDA/MAA submissions and responses to Health Agency questions
- check_circleOversee CRO and vendor performance regarding study start-up and conduct
- check_circleLead medical review of critical data, serious adverse events, and data query resolution
- check_circleAssist in protocol writing and ensure high-quality development of study protocols and standards
- check_circleCollaborate with functional partners to ensure integrated execution and oversight of late-stage oncology studies
Requirements
- verifiedMinimum Advanced Degree in Medicine (M.D. or equivalent)
- verifiedBoard certified or Board eligible Uro-Oncologist/Oncologist
- verifiedApplicable post-doctoral fellowship training
- verifiedMinimum 3+ years experience in relevant urology/oncology clinical research
- verifiedStrong oral, written communication and presentation skills
- verifiedExperience working in a matrix team environment with cross-functional teams
- verifiedAbility to use influencing skills
Nice to Have
Business Savvy, Clinical Research and Regulations, Clinical Trials, Collaborating, Consulting, Data Management and Informatics, Design Mindset, Drug Discovery Development, Industry Analysis, Innovation, Market Research, Regulatory Affairs Management, Research Ethics, Scientific Evaluation, Scientific Research, Stakeholder Management, Strategic Analysis
Benefits & Perks
check_circleConsolidated retirement plan (pension) and 401(k) savings plancheck_circleLong-term incentive program eligibilitycheck_circle120 hours of vacation per calendar yearcheck_circle40 hours of sick time per calendar year (varies by state)check_circle13 days of holiday pay including floating holidayscheck_circleUp to 40 hours of work, personal, and family time per calendar yearcheck_circle480 hours of parental leave within one year of birth, adoption, or foster carecheck_circle240 hours of bereavement leave for immediate family memberscheck_circle80 hours of caregiver leave in a 52-week rolling periodcheck_circle32 hours of volunteer leave per calendar year
Similar Job Opportunities
Skills, education and keywords
Skills: Clinical Research, Clinical Trials, Data Management, Drug Discovery Development, Regulatory Affairs Management, Research Ethics, Scientific Evaluation, Scientific Research.
Education: Minimum Advanced Degree in Medicine (M.D.) required.
Frequently asked questions about Medical Director, Study Responsible Physician at Johnson & Johnson
What does a Medical Director, Study Responsible Physician at Johnson & Johnson do?expand_more
A Medical Director, Study Responsible Physician at Johnson & Johnson is responsible for the following: Lead project scientists and provide mentoring, training, and supervision for clinical study teams; Co-lead authorship of informed consent forms, study manuals, clinical study reports, and regulatory documents; Review external clinical research proposals and manuscripts prepared for publication; and Act as liaison between the company and clinical investigators while building relationships with opinion leaders.
What are the requirements for this Medical Director, Study Responsible Physician role?expand_more
To qualify for the Medical Director, Study Responsible Physician at Johnson & Johnson position, applicants should have: Minimum Advanced Degree in Medicine (M.D. or equivalent); Board certified or Board eligible Uro-Oncologist/Oncologist; Applicable post-doctoral fellowship training; Minimum 3+ years experience in relevant urology/oncology clinical research; Strong oral, written communication and presentation skills; and Experience working in a matrix team environment with cross-functional teams.
Where is the Medical Director, Study Responsible Physician role at Johnson & Johnson located?expand_more
Medical Director, Study Responsible Physician at Johnson & Johnson is based in Spring House Tavern, 1032, North Bethlehem Pike, Spring House, Lower Gwynedd Township, Montgomery County, Pennsylvania, 19477, United States. This is a on-site role.
Is this Medical Director, Study Responsible Physician job remote, hybrid, or on-site?expand_more
Johnson & Johnson has listed this Medical Director, Study Responsible Physician role as on-site.
How much experience is required for this Medical Director, Study Responsible Physician role?expand_more
Medical Director, Study Responsible Physician at Johnson & Johnson typically requires 3+ years of relevant experience at the lead level.
What skills do you need for the Medical Director, Study Responsible Physician role at Johnson & Johnson?expand_more
Key skills for Medical Director, Study Responsible Physician at Johnson & Johnson include Clinical Research; Clinical Trials; Data Management; Drug Discovery Development; Regulatory Affairs Management; Research Ethics; Scientific Evaluation; and Scientific Research.
What education is required for Medical Director, Study Responsible Physician at Johnson & Johnson?expand_more
Educational requirements for this role: Minimum Advanced Degree in Medicine (M.D.) required.
What category does the Medical Director, Study Responsible Physician role belong to?expand_more
Medical Director, Study Responsible Physician at Johnson & Johnson is part of the scientific & qa job category on Recrutus.