Exelixis

Executive Director, Scientific Publications (Oncology)

Exelixis$273K — $388K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • Doctorate degree (PharmD, MD, PhD) with 15+ years experience, or
  • Master's degree in related discipline with 16+ years experience, or
  • Bachelor's degree in related discipline with 18+ years experience, or
  • Equivalent combination of education and experience.
  • Oncology experience highly preferred.

Responsibilities

  • Lead the Publications team, including hiring and development.
  • Oversee publication planning for development molecules and alignment with cross-functional teams.
  • Manage execution of publication projects, including writing and editing as needed.
  • Partner with stakeholders to ensure timely delivery of abstracts, posters, and manuscripts.
  • Select and manage publication vendors, including contracts and budgeting.
  • Maintain electronic support functions for Publications, including portals and archives.
  • Collaborate with Medical Affairs to support functional area deliverables.

Benefits

  • Comprehensive medical, dental, and vision coverage.
  • 401k plan with generous company contributions.
  • Discretionary annual bonus program.
  • 15 vacation days in the first year and 17 paid holidays.
  • Comfortable modern workspace with necessary equipment.
Full Job Description
SUMMARY/JOB PURPOSE:

The Executive Director, Scientific Publications leads the publication planning and execution functions at Exelixis. Responsibilities include management of the Publications team, oversight of publication planning for each Exelixis development compound, coordination of publication planning and tactical execution with cross-functional collaborators, contribution to publication project execution as needed, management of publication vendors and responsibility for compliance aspects of the publication function. This role provides an outstanding opportunity to lead in a cross-functional environment. Strong communication, leadership, and project and people management skills are essential to success.

Essential Duties And Responsibilities:
  • Lead the Publications function as part of Scientific Publications, including group organization, hiring, and employee development
  • Oversee the publication planning process for each ongoing development molecule, including development of scientific platforms (as needed) and publication plans, regular cross-functional meetings to gain input and alignment, coordination with alliance partner publication functions as needed
  • Oversee tactical execution of publication projects as per publication plans, including contribution to concept development, data analysis, writing, and editing as needed
  • Partner with internal and external stakeholders; ensure execution of abstracts, posters, oral presentations, and manuscripts in accordance with timelines as set in publication plans.
  • Oversee publication vendors including vendor selection, contract development and budgeting
  • Oversee electronic support functions for Publications, including the publication portal and archives
  • Manage the Publications SOP and oversight of internal publications review and approval process
  • Operate in accordance with all Exelixis SOPs, including the Publications SOP, and promote the adoption of working standards consistent with Good Publication Practice.
  • Collaborate with other members of the Medical Affairs organization in support of their functional area deliverables.
  • Develop product and disease state expertise, keep abreast of the changing drug development environment.


Supervisory Responsibilities:
  • Supervises staff, including hiring, scheduling, and assigning work, reviewing performance, and recommends salary increases, promotions, transfers, demotions, or terminations.
  • Provide direction to other individuals.


EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS:

Education/Experience:
  • Doctorate level degree (PharmD, MD, PhD) with a minimum of 15 years of related experience; or,
  • Master's level degree in related discipline and a minimum of 16 years of related experience; or,
  • Bachelor's level degree in related discipline and a minimum of 18 years of related experience; or,
  • Equivalent combination of education and experience.


Experience/The Ideal for Successful Entry into Job:
  • Oncology experience highly preferred.
  • Experience in pharmaceutical/biotech business.
  • Significant experience with publication development, writing, and management is required.


Knowledge/Skills:
  • Understanding of the pharmaceutical/biotech business and related regulations, guidelines, standards, and practices.
  • Familiarity with the principles of health care compliance.
  • Demonstrated ability to lead initiatives, manage projects and work cross-functionally.
  • Skilled medical/technical writer.
  • Self-motivated, organized, problem-solving, solution-oriented, collaborative team player.
  • Able to act independently and assume responsibility for multiple initiatives in a fast-faced environment yet remain flexible in response to changing needs and competing demands.
  • Strong skills with regard to written and verbal communication of complex medical and scientific data to a variety of audiences.


JOB COMPLEXITY:
  • Works in a fast-paced, small-team environment that is growing and evolving. This position requires regular reprioritization of projects while adhering to timelines and achievement of deliverables.


Working Conditions:
  • Periodic travel required (approximately 20%) to support medical affairs activities at scientific congresses and company meetings, and to provide oversight to external contracted organizations.


DISCLAIMER

The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.

#LI-MB1

Our compensation reflects the cost of labor across several U.S. geographic markets, and we pay differently based on those defined markets. The base pay range for this position is $273,000 - $388,000 annually. The base pay range may take into account the candidate's geographic region, which will adjust the pay depending on the specific work location. The base pay offered will take into account the candidate's geographic region, job-related knowledge, skills, experience and internal equity, among other factors.

In addition to the base salary, as part of our Total Rewards program, Exelixis offers comprehensive employee benefits package, including a 401k plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. Employees are also eligible for a discretionary annual bonus program, or if field sales staff, a sales-based incentive plan. Exelixis also offers employees the opportunity to purchase company stock, and receive long-term incentives, 15 accrued vacation days in their first year, 17 paid holidays including a company-wide winter shutdown in December, and up to 10 sick days throughout the calendar year.

If you have a disability and need an accommodation in relation to the application and/or recruitment process, please email us at:

WORKING CONDITIONS:

Our office is a modern space that fosters collaboration and creativity. Teams work closely together, sharing ideas and solutions in a supportive atmosphere. We provide all necessary equipment, including dual monitors and ergonomic chairs, to ensure a comfortable workspace.

DISCLAIMER:
The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.

About Exelixis

Exelixis is a biotechnology company that develops and commercializes innovative medicines for the treatment of cancer. The company's flagship product, CABOMETYX® (cabozantinib), is an inhibitor of multiple tyrosine kinases, including MET, AXL, and VEGFR, which are involved in the growth and spread of cancer cells. CABOMETYX is approved in the United States for the treatment of advanced renal cell carcinoma (RCC) and hepatocellular carcinoma (HCC), and is also approved in the European Union and other countries for the treatment of advanced RCC. Exelixis is headquartered in Alameda, California, and has additional offices in South San Francisco, California, and Basel, Switzerland. Learn more at www.exelixis.com.
Learn more about Exelixis
Size
954 employees
Market Cap
$5 billion
Industry
Net Income
$111.7 million
5 Year Trend
+49.6%
Revenue
$987.5 million
NASDAQ

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