Associate Director*

The Fountain Group; Elkhorn (CA); Hybrid; USD 124,000 - 141,000; Full time

Benefits offered by this job

Hybrid schedule

Job summary

The Fountain Group is seeking an Associate Director for a prominent client. The role is based in multiple locations including Raleigh, Foster City, Santa Monica, or Parsippany on a hybrid schedule.

The assignment is 6 months with potential extension or conversion based on performance and budget. You will respond to complex medical inquiries, develop Medical Information content, and support launch readiness for multiple myeloma programs while collaborating with Medical Affairs, Clinical

Qualifications

• Advanced scientific or medical degree (MD/PhD/PharmD).
• Minimum of 5 years Medical Information experience.

Responsibilities

• Respond to complex medical and scientific inquiries using literature and data.
• Develop, review, and maintain Medical Information content.
• Support product launch readiness for multiple myeloma by developing resources.
• Collaborate cross-functionally with Medical Affairs, Clinical Development, Regulatory, Quality, and Patient Safety teams.
• Monitor literature, data, and regulatory updates to ensure accuracy and compliance.
• Analyze inquiry trends, oversee vendor deliverables, provide scientific training, and maintain documentation.

Skills

Medical information experience

Scientific writing

Cross-functional collaboration

Project management

Education

MD/PhD/PharmD

Job description

The Fountain Group is currently seeking an Associate Director for a prominent client of ours. This position is located in Raleigh, NC, Foster City, CA, Santa Monica, CA or Parsippany, NJ. Details for the position are as follows:

• Pay: $90-102.49/hr.
• Hybrid schedule
• 6‑month assignment with possibility for extension or conversion based on performance and budget.

Responsibilities

• Respond to complex medical and scientific inquiries using clinical literature, approved response documents, and evidence-based data.
• Develop, review, and maintain Medical Information content, including standard response letters, FAQs, and scientific Q&A documents.
• Support product launch readiness for multiple myeloma by developing scientific resources and preparing internal and external support teams.
• Collaborate cross-functionally with Medical Affairs, Clinical Development, Regulatory, Quality, and Patient Safety teams.
• Monitor scientific literature, clinical data, and regulatory updates to ensure content accuracy and compliance.
• Analyze inquiry trends, oversee vendor deliverables, provide scientific training, and maintain accurate documentation.

Qualifications

• Advanced scientific or medical degree, such as an MD, PhD, or PharmD.
• Minimum of 5 years of Medical Information experience within the pharmaceutical or biopharmaceutical industry preferred.
• Experience managing complex medical inquiries and developing scientific response materials.
• Strong knowledge of clinical literature, pharmaceutical regulations, safety requirements, and Medical Information compliance standards.
• Excellent scientific writing, communication, critical thinking, project management, and cross‑functional collaboration skills.
• Hematology/oncology, multiple myeloma, cell therapy, or product launch experience preferred.

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