Medical Director or Scientific Director, Medical Affairs - Multiple Myeloma

Hispanic Alliance for Career Enhancement; San Francisco (CA); Remote; USD 200,000 - 300,000; Full time

Job summary

A leading company in the pharmaceutical industry is seeking a Medical Director or Scientific Director for their Medical Affairs team. This role involves providing strategic medical input, overseeing clinical studies, and collaborating with cross-functional teams. Candidates with a strong background in multiple myeloma and clinical trials are preferred. The position offers competitive compensation and comprehensive benefits, including health insurance and paid time off.

Benefits

Health Insurance

401(k)

Paid Time Off

Qualifications

• At least 2 years clinical trial or medical affairs experience; 3+ years preferred.
• Knowledge of clinical trial methodology, data analysis, and regulatory requirements.

Responsibilities

• Initiate medical affairs activities and data dissemination supporting scientific strategy.
• Design, analyze, interpret, and report scientific data for protocols and regulatory submissions.
• Manage budgets, timelines, and compliance for scientific activities.

Skills

Communication

Leadership

Education

M.D.

PhD

Job description

Medical Director or Scientific Director, Medical Affairs - Multiple Myeloma

Employer: AbbVie
Location: San Francisco, California, US
Salary: Competitive
Closing date: May 12, 2025

Sector: Academic / Research
Field: Conservation science
Discipline: Statistics
Job Level: Senior level
Salary Type: Salary
Employment Type: Fellowship

Company Description
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 aim to have a remarkable impact on people's lives across key therapeutic areas including immunology, oncology, neuroscience, and eye care, along with our products in the Allergan Aesthetics portfolio. For more information, visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn, and TikTok.

Job Description
*Preferred locations include Lake County, IL; Florham Park, NJ; or San Francisco, CA. Remote candidates will also be considered.
*Position title will be based on qualifications listed below.

Purpose:

The Director provides strategic and operational medical and scientific input into core medical affairs activities such as healthcare professional interactions, data generation, educational initiatives, and patient safety. Works closely with sales, marketing, and commercial teams to support medical and brand strategies, promotional activities, and market access.

Responsibilities:

• Initiate medical affairs activities and data dissemination supporting scientific strategy.
• Design, analyze, interpret, and report scientific data for protocols, Investigator Brochures, Clinical Study Reports, and regulatory submissions.
• Oversee clinical studies, monitor study integrity, and communicate safety and efficacy data. Responsible for study timelines and enrollment.
• Provide clinical expertise on multiple myeloma, coordinate scientific activities, and participate in business development as needed.
• Act as a scientific interface, supporting cross-functional collaboration and integrating perspectives into clinical development plans.
• Lead development of medical and evidence plans, and train internal teams globally.
• Support the creation of marketing materials, medical education, and scientific communications.
• Coordinate scientific activities with internal stakeholders and serve as a scientific team interface for regulatory discussions.
• Educate investigators and team members on therapeutic areas, staying current with literature and conferences.
• Manage budgets, timelines, and compliance for scientific activities.

Qualifications:

Medical Director:

• M.D. or equivalent (D.O., non-US M.D.) with preferred multiple myeloma experience.
• At least 2 years clinical trial or medical affairs experience; 3+ years preferred.
• Knowledge of clinical trial methodology, data analysis, and regulatory requirements.
• Ability to independently run clinical studies and lead cross-functional teams.
• Excellent communication skills in English.

Scientific Director:

• PhD or PharmD with additional postdoctoral experience preferred.
• 10-15 years in the pharmaceutical industry, with substantial therapeutic area expertise.
• 7-10 years in Medical Affairs, with global experience preferred.
• 4+ years managing clinical trials.
• Strong leadership and communication skills.

Additional Information:

The compensation range is indicative and may vary based on location and other factors. Benefits include paid time off, health insurance, 401(k), and participation in incentive programs. Pay is contingent upon actual earnings, vesting, and company discretion. AbbVie is an equal opportunity employer committed to diversity and inclusion. For more details, visit here and here.