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Home Based Prostate Cancer Jobs (NOW HIRING)

Spearhead the development and expansion of a growing prostate cancer program within our urology ... Paid occurrence based malpractice * Residency/Training Stipend * Student Loan repayment and ...

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Home Based Prostate Cancer information

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$90.5K

$121.7K

$155.5K

How much do home based prostate cancer jobs pay per year?

As of Jul 22, 2026, the average yearly pay for home based prostate cancer in the United States is $121,666.00, according to ZipRecruiter salary data. Most workers in this role earn between $106,000.00 and $137,500.00 per year, depending on experience, location, and employer.

What is the difference between Home Based Prostate Cancer vs Home Based Breast Cancer Patient Support Specialist?

AspectHome Based Prostate CancerHome Based Breast Cancer Patient Support Specialist
CredentialsMedical knowledge, counseling certificationMedical knowledge, counseling certification
Work EnvironmentHome-based, patient interactionHome-based, patient interaction
Industry UsageHealthcare, patient supportHealthcare, patient support
Common Search/ComparisonYesYes

Both roles involve providing support and information to patients with cancer, often from a home setting. The main difference lies in the specific cancer type they focus on—prostate versus breast cancer—requiring specialized knowledge related to each condition. Both positions typically require similar credentials and serve similar functions within healthcare support services.

More about Home Based Prostate Cancer jobs
What cities are hiring for Home Based Prostate Cancer jobs? Cities with the most Home Based Prostate Cancer job openings:
What are the most commonly searched types of Prostate Cancer jobs? The most popular types of Prostate Cancer jobs are:
What states have the most Home Based Prostate Cancer jobs? States with the most job openings for Home Based Prostate Cancer jobs include:
Infographic showing various Home Based Prostate Cancer job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 78% Full Time, 14% Part Time, and 7% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $121,666 per year, or $58.5 per hour.
Scientific Director / Senior Medical Director, Medical Affairs - Global Oncology Pipeline (Prostate

Scientific Director / Senior Medical Director, Medical Affairs - Global Oncology Pipeline (Prostate

AbbVie

Florham Park, NJ • On-site

$182K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 21 days ago


Job description

Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
The Medical Affairs organization provides patients, healthcare providers, and payers everywhere with the practical and clinically relevant information and solutions they need to use AbbVie products safely and effectively, throughout the product lifecycle and the patient's journey.
The Scientific Director / Senior Medical Director, Medical Affairs - Global Oncology Pipeline provides medical and scientific input into core strategic and operational pipeline medical affairs activities for the prostate cancer portfolio such as: health-care professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, scientific communications, and value proposition) and safeguarding patient safety (risk minimization activities and safety surveillance activities). Works closely with sales, marketing, and commercial teams to provide strategic medical input into core brand (product) strategies, and to support medical affairs, marketing activities (promotional material generation and product launches) and market access.
This position can be based at our Mettawa, IL, Florham Park, NJ, or South San Francisco, CA locations and will follow a hybrid schedule of Tuesdays-Thursdays in office.
Responsibilities
  • Leads medical input into disease area strategy and asset strategies within the prostate cancer oncology pipeline portfolio.
  • Leads pipeline medical evidence generation strategy and execution including company sponsored studies, research collaborations and investigator initiated studies.
  • Provides in-house medical expertise for the disease area and assets, coordinating appropriate scientific activities with internal and external stakeholders as they relate to ongoing programs. May participate in due diligence or other business development activity as required by program needs, and contribute to translational strategy in partnership with discovery colleagues.
  • Acts as a medical interface and actively solicits insights and opinion through the development and execution of medical expert engagement strategies, partnering with clinical development, commercial, access, area and affiliate colleagues to ensure that broad perspectives both internally and externally are incorporated into strategies and plans as appropriate.
  • Leads creation of early scientific narratives, messaging, and communications activities including congress planning, medical education, publication strategies and plans.
  • May assist in the development of scientifically accurate marketing materials, medical education programs, advisories, and symposia. Assists with the scientific review, development, approval, execution, and communication of affiliate/area/global medical affairs sponsored or supported clinical research activities.
  • May interact with and coordinates appropriate scientific and medical activities with internal stakeholders (i.e., commercial, clinical operations, discovery, statistics, regulatory, etc...) as they relate to on-going medical affairs projects. Serves as the scientific team interface for key regulatory discussions.
  • Provide scientific/medical education to investigators, clinical monitors, and Global Project Team members related to therapeutic area or disease specific information. Keeps abreast of professional information and technology through conferences and/or medical literature and acts as a therapeutic area resource.
  • Ensures budgets, timelines, compliance requirements are factored into programs' scientific activities.

Qualifications
Position will be commensurate with experience.
Scientific Director Qualifications:
  • Advanced Degree PhD or PharmD. Additional post doctorate experience highly preferred.
  • Typically, 10-15 years of experience in the pharmaceutical industry or equivalent
  • 7-10 years of experience in Medical Affairs with Global Medical Affairs experience highly preferred.
  • Substantial knowledge of relevant therapeutic area required. Direct experience and knowledge in prostate cancer strongly preferred.
  • Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
  • Proven leadership skills in a cross-functional global team environment.
  • Must possess excellent oral and written English communication skills.

Senior Medical Director Qualifications:
  • Medical Doctorate (M.D.) degree or equivalent (D.O. or non-US equivalent of M.D). Relevant therapeutic specialty in an academic or hospital environment preferred. Completion of residency and/or fellowship is preferred.
  • Minimum of 2 years of clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent. 3+ years of experience is preferred.
  • Substantial knowledge of relevant therapeutic area required. Direct experience and knowledge in prostate cancer strongly preferred.
  • Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
  • Proven leadership skills in a cross-functional global team environment
  • Ability to interact externally and internally to support global business strategy.
  • Must possess excellent oral and written English communication skills.

Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html

AbbVie logo

About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013