Top 4504 Medical director Jobs in Matawan, Nj

Medical Director
Genmab —Princeton, NJ
- $261,120 - $391,680 a year
- Online Application
- Medicine
- 3 years
- Continuous improvement
- Commuter assistance
- Paid parental leave
Food Service Director in Assisted Living
Benchmark Senior Living —Scotch Plains, NJ
- $80,000 - $88,000 a year
- Mid-level
- Ability to lift 50 pounds
- Team management
- Disability insurance
- Health insurance
4d
Director of Social Services
Shore Pointe Care Center —Eatontown, NJ
- Full-time
- Senior level
Quick Apply
Associate Director, R&D Strategic Initiatives
Genmab —Princeton, NJ
- $160,880 - $241,320 a year
- Online Application
- 8 years
- Bachelor's degree
- Continuous improvement
- Commuter assistance
- Paid parental leave
Nurse Practitioner/Physician Assistant
AXA Medical —Woodbridge, NJ
- $60 - $75 an hour
- Full-time
- BLS Certification
- HIPAA
- Mid-level
- Health insurance
- Paid time off
Quick Apply
4d
Program Director
Rutgers University —Piscataway, NJ
- $122,434 a year
- Full-time
- Doctoral degree
- Ability to walk for extended periods
- Licensed Clinical Social Worker
- Paid holidays
- Dental insurance
13d
Director, Counseling Center
Rutgers University —Newark, NJ
- $124,967 a year
- Full-time
- Microsoft Excel
- 5 years
- Computer literacy
- Paid holidays
- Dental insurance
Executive Director of University Medical Group (UMG)
University HealthCare Alliance —Newark, NJ
- $99.70 - $132.11 an hour
- Full-time
- Hybrid work
- Hospital
- 5 years
- Bachelor of Science
Director of Employment and Day Habilitation Services
EasterSeals of New Jersey —New Brunswick, NJ
- Full-time
- Data analysis skills
- Master's degree
- Analysis skills
- Paid training
- Wellness program
Quick Apply
Director of Anesthesia Operations I - New Jersey
Envision Healthcare —Jersey City, NJ
- $149,000 - $190,000 a year
- Full-time
- Hybrid work
- Master's degree
- Bachelor's degree
- Operating room
- Paid holidays
- Disability insurance
Clinical Research Specialist - Skin Health/Personal Care
Colgate-Palmolive —Piscataway, NJ
- $96,800 - $137,000 a year
- Hybrid work
- Mid-level
- Master's degree
- Bachelor's degree
- Profit sharing
- Paid parental leave
13d
Director, Access Programs
Insmed Incorporated —Bridgewater, NJ
- $177,000 - $242,000 a year
- Full-time
- Remote
- Bachelor's degree
- Travel
- Senior level
- Employee stock purchase plan
- Disability insurance
10d
Clinical Research Specialist - Skin Health/Personal Care (175269)
Colgate-Palmolive —Piscataway, NJ
- $96,800 - $137,000 a year
- Hybrid work
- Mid-level
- Master's degree
- Bachelor's degree
- Profit sharing
- Paid parental leave
13d
Director of Clinical Admissions
Charlie Health —New York, NY
- $106,000 - $135,000 a year
- Weekends as needed
- Remote
- Google Workspace
- 5 years
- HIPAA
- Health insurance
- Dental insurance
Quick Apply
Executive Director of Information Technology
Rutgers University —New Brunswick, NJ
- $180,910 a year
- Full-time
- 5 years
- Writing skills
- Office
- Paid holidays
- Dental insurance
4d
Crisis Clinician - Part Time - 22.5 Hours - Evenings, 4PM-12AM - Atlantic Health Overlook Medical Center, NJ
Atlantic Health System —Summit, NJ
- Part-time
- Psychiatry
- Licensed Clinical Social Worker
- LPC
7d
Director, Environmental Services
Hudson Regional Hospital —Bayonne, NJ
- $90,000 - $100,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Hospital
- Paid holidays
- Health insurance
Quick Apply
Medical Director, Doctronic
Doctronic —New York, NY
- $250,000 - $300,000 a year
- Full-time
- Remote
- Medicine
- Supervising experience
- Patient care
Associate Medical Review Director
Novo Nordisk —Plainsboro, NJ
- $165,000 - $220,000 a year
- Medicine
- Computer literacy
- English
- Disability insurance
- Health insurance
Director, Medical Information
Compass Pathways —New York, NY
- $210,000 - $255,000 a year
- Remote
- Medicine
- Doctor of Philosophy
- Travel
Quick Apply
7d

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Medical Director

Genmab -
Princeton, NJ

Apply Now

Job Details

Full-time
$261,120 - $391,680 a year

Benefits

Commuter assistance
Paid parental leave
Health savings account
Paid holidays
Health insurance
Dental insurance
Tuition reimbursement
Parental leave
Vision insurance
401(k) matching

Qualifications

Doctor of Medicine
Team leadership
Team development
Team training
Managing clinical research teams
Leading team collaboration initiatives
Oncology
Clinical trial support in drug product development
Pharmaceutical research experience
Team building

Full Job Description

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees.

Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so.

Does this inspire you and feel like a fit? Then we would love to have you join us!

The Role:

We are looking for an experienced and dedicated Medical Director to be a part of our Global Clinical Development Team.

The Medical Director will be accountable for the medical oversight of one or more clinical trials, medical review and communication of data, and medical input into regulatory documents and presentations.

Responsibilities:

Lead the development of the program strategy for assigned trials/compounds and participate in the development of the clinical development plan (CDP).
Lead creation and review of clinical components of key documents, clinical and regulatory documents, annual safety updates, and registration dossiers (ie, protocol, ICF, IB, annual safety updates, study reports, regulatory submissions [Briefing documents, IND, Clinical dossiers] supporting registration, market access, and commercialization of the compound(s).
Oversee early-stage programs and develop clinical programs including component studies.
Oversee safety of the drug, including the safety aspects of patients in clinical studies and signal detection with support of the Safety physician
Create, integrate, and execute overall medical strategies of assigned clinical development programs; provide strategic medical advice on potential new projects (internal & external).
Contribute to publication and clinical communication strategy in coordination with Scientific Communications; provide inputs to key external presentations
Provide strategic input and development support for clinical plans and individual trial protocols.
Interact with key opinion leaders to ensure implementation of the latest clinical and medical thinking and guidelines into clinical development plans, as well as consideration of novel medical methods development and new potential targets.
Contribute to medical department best practices, standardization and to cross-functional process improvements.
Support the development of case report forms, perform medical monitoring, liaise with investigators and site personnel, perform preliminary and exploratory data analyses on clinical trials, author clinical study reports, provide input on publication materials, and participate in advisory boards.
Support the development of other relevant documents that are necessary for the advancement of the product pipeline.
Serve as medical and technical resource for clinical issues raised by internal and external collaborators, investigators, consultants and contractors.
Create medical deliverables: clinical development plans, concept sheets, briefing books, and label and marketing application dossier.
Contribute to medical input to preclinical development of candidate therapeutic antibodies.
Drive and monitor quality of all clinical documents (e.g., Investigators’ Brochures, protocols, study reports, clinical components of regulatory submissions, safety documents) produced by CDT.
Participate in multi-function teams necessary for the advancement of the product pipeline.
Attend relevant congresses or other relevant fora to maintain up-to-date scientific/medical knowledge.

Requirements:

MD degree.
Minimum of 3+ years of directly related industry experience in oncology clinical development, including experience leading or supporting Phase 3 clinical studies.
Clinical experience in oncology required; experience in solid tumors preferred.
Proven ability to build and lead teams and inspire trust among colleagues.
Experience representing team and organization in a variety of internal/external settings.
Experience training and managing team members.
Proven performance in earlier role/comparable role.

For US based candidates, the proposed salary band for this position is as follows:

$261,120.00-$391,680.00

The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location. Also, certain positions are eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives.

When you join Genmab, you’re joining a culture that supports your physical, financial, social, and emotional wellness. Within the first year, regular full-time U.S. employees are eligible for:

401(k) Plan: 100% match on the first 6% of contributions
Health Benefits: Two medical plan options (including HDHP with HSA), dental, and vision insurance
Voluntary Plans: Critical illness, accident, and hospital indemnity insurance
Time Off: Paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave
Support Resources: Access to child and adult backup care, family support programs, financial wellness tools, and emotional well-being support
Additional Perks: Commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses

Further details on eligibility for compensation and benefits based on role will be provided during the recruitment process

About Genmab

Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab’s vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO®) antibody medicines.

Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com and follow us on LinkedIn and X.

Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice (genmab.com).

Please note that if you are applying for a position in the Netherlands, Genmab’s policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.

Apply Now

Refine Your Search

medical director jobs in matawan, nj

Medical Director

Food Service Director in Assisted Living

Director of Social Services

Associate Director, R&D Strategic Initiatives

Nurse Practitioner/Physician Assistant

Program Director

Director, Counseling Center

Executive Director of University Medical Group (UMG)

Director of Employment and Day Habilitation Services

Director of Anesthesia Operations I - New Jersey

Clinical Research Specialist - Skin Health/Personal Care

Director, Access Programs

Clinical Research Specialist - Skin Health/Personal Care (175269)

Director of Clinical Admissions

Executive Director of Information Technology

Crisis Clinician - Part Time - 22.5 Hours - Evenings, 4PM-12AM - Atlantic Health Overlook Medical Center, NJ

Director, Environmental Services

Medical Director, Doctronic

Associate Medical Review Director

Director, Medical Information

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