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Exelixis

Remote Job Openings at Exelixis (5)

Sr Regulatory Operations Manager

United States $165K - $208K per year 5-10 yrs exp Legal

Manage and execute regulatory submission planning, publishing, and lifecycle management for clinical and commercial programs. Collaborate on process improvements and automation to ensure high-quality, compliant submissions that meet Health Authority requirements.

Patient Recruitment & Retention Strategy & ICF Governance Director (Biotech / Oncology)

United States $185K - $234K per year 10+ yrs exp Recruitment

The director leads the implementation of global patient recruitment and retention strategies while managing cross-functional informed consent governance. They collaborate with internal teams and external partners to ensure clinical trials meet enrollment goals while maintaining strict adherence to regulatory guidelines.

GU Field Based Marketing Director - Key Customer Team (Remote North East - NY, MA & CT)

United States $204K - $290K per year 10+ yrs exp Marketing

The role focuses on building relationships with Key Opinion Leaders to drive brand strategy and execute marketing tactics within the oncology segment. The director acts as a primary liaison between field-based customers and home office cross-functional teams to ensure effective product positioning.

Senior Oncology Account Manager - (Birmingham, AL | Remote)

United States $198K - $253K per year 5-10 yrs exp Sales

The Senior Oncology Account Manager will drive strategic growth and commercial impact within a complex territory by leveraging market insights and building relationships with healthcare providers. The role involves mentoring peers, executing account plans, and representing field perspectives in brand planning and cross-functional initiatives.

Clinical Development Medical Director (Biotechnology / Oncology)

United States $254K - $361K per year 5-10 yrs exp Healthcare

Lead and execute early and late-stage clinical trials for oncology products, including the design and planning of study protocols. Act as a medical monitor and collaborate with internal safety groups to analyze and report clinical trial data to regulatory agencies.