Exelixis

Associate Regulatory Operations Director

Exelixis$157K — $222K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a related discipline with 11+ years of experience, or Master's degree with 9+ years, or PhD with 5+ years, or equivalent combination.
  • Extensive knowledge of global regulatory submission requirements.
  • Proficient in developing and managing project plans with established timelines.
  • Strong verbal and written communication skills, presenting clearly to diverse audiences.
  • Ability to build collaborative relationships across cross-functional teams.

Responsibilities

  • Oversee and plan all regulatory submissions in electronic format.
  • Ensure clarity and efficiency in submission processes and timelines.
  • Collaborate with Regulatory Affairs to maintain global submission project plans.
  • Lead cross-functional teams to explore and optimize submission processes.
  • Develop best practices for submission planning and implement major timelines.
  • Identify IT solutions to enhance regulatory operations systems.
  • Mentor team members on submission planning best practices.

Benefits

  • Comprehensive medical, dental, and vision coverage.
  • 401k plan with generous company contributions.
  • Discretionary annual bonus program and stock purchase opportunity.
  • 15 accrued vacation days in the first year and 17 paid holidays.
  • Modern office environment that supports collaboration and creativity.
Full Job Description
SUMMARY/JOB PURPOSE:

The Associate Regulatory Operations Director is responsible for overseeing submission activity for the company's submission portfolio, with first line accountability for managing the submission forecast and ensuring proper staffing for upcoming submissions. She/he utilizes in-depth knowledge of global regulatory submission requirements and works collaboratively within Regulatory Affairs and other cross-functional departments in providing guidance towards achieving department application filing objectives , identifying areas of concern that are impacting submission timelines, drive process efficiencies and overall operational effectiveness for timely and high-quality regulatory submissions. This role also provides oversight and guidance on the Veeva RIM suite and identify best practices for effective implementation.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
  • Oversees the planning of all regulatory submissions (INDs, NDAs, BLAs, supplemental applications, etc.) in electronic format.
  • Accountable for the oversight of regulatory submission processes and best practices, bringing clarity to submission timelines and deliverables.
  • Works collaboratively with Regulatory Affairs and contributing cross-functional team members in order to create and maintain global regulatory submission project plans, manages deliverable timelines and activities, ensures alignment on roles and responsibilities, and that any issues, risks, or impact due to changes in strategy and/or timelines are assessed quickly throughout the submission process ensuring transparency of submission status to key stakeholders and management.
  • Leads a cross-functional team within Exelixis to explore submission process optimization.
  • Develops submission planning best practices and implementation of major submission timelines.
  • Partners with Vice President, Regulatory Operations in the development and implementation of Department best practices and ways of working.
  • Provides key insight to identify IT solutions to enhance Regulatory Operations systems (i.e., Project planning tools, Veeva RIM)
  • Participates in the writing of regulatory processes (SOPs, work instructions, and/or internal guidelines) and other departmental initiatives to improve standards and systems internally.
  • Mentors/instructs members of the Regulatory Operations team on Best Practices for submission planning.
  • Reviews and interprets regulatory guidelines.


SUPERVISORY RESPONSIBILITIES:
  • None.


EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS:

Education/Experience:
  • Bachelor's degree in related discipline and a minimum of eleven years of related experience; or,
  • Master's degree in related discipline and a minimum of nine years of related experience; or,
  • PhD degree in related discipline and a minimum of five years of related experience; or,
  • Equivalent combination of education and experience.


Experience/The Ideal for Successful Entry into Job:

Knowledge/Skills:
  • Develops and manages plans within established timelines and balances commitments to complete multiple activities and achieve results. Takes pride in delivering high quality work.
  • Applies wide knowledge of the regulatory framework and industry practices to develop innovative approaches and complete complex work.
  • Demonstrates clear and effective verbal and written communication. Provides timely and appropriate information updates. Speaks clearly and confidently in one-to-one situations and effectively presents information to groups of departmental colleagues.
  • Strong interpersonal skills and ability to accommodate differing views to actively support the development of an agreed upon resolution.
  • Manages effectively performing teams to achieve common objectives. Engages internal stakeholders to establish productive collaborative relationships.
  • Applies knowledge of organizational goals and objectives and demonstrates skill and insight in gathering, analyzing and applying key information to solve problems.
  • Leads self and others; acts with integrity and builds trust with colleagues to contribute to accomplishing team objectives.


JOB COMPLEXITY:
  • Capable of managing the execution of multiple tasks.
  • Ensures appropriate prioritization and execution for area of responsibility.
  • Proactively anticipates, prioritizes and resolves task-related challenges.
  • Designs and implements solutions to address task-related challenges, taking into consideration the broader impact.


WORKING CONDITIONS:
  • Travel approximately 20%


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 $157,500 - $222,500 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.

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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