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Senior Director, Regulatory Affairs

Contineum TherapeuticsSan Diego, CA

$240,000 - $265,000 / year

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Overview

Schedule
Full-time
Career level
Executive
Remote
Remote
Compensation
$240,000-$265,000/year
Benefits
Health Insurance
Dental Insurance
Vision Insurance

Job Description

Company Overview: Contineum Therapeutics (Nasdaq: CTNM) is a clinical-stage biopharmaceutical company pioneering novel, oral small molecule therapies for NI&I indications with significant unmet need.  Contineum is advancing a pipeline of internally-developed programs with multiple drug candidates now in clinical trials.  PIPE-791 is an LPA1 receptor antagonist in clinical development for idiopathic pulmonary fibrosis and chronic pain.  PIPE-307 is a selective inhibitor of the M1 receptor in clinical development for relapsing-remitting multiple sclerosis and major depressive disorder.  For more information, please visit www.contineum-tx.com.

The Senior Director of Regulatory Affairs leads global regulatory activities and manages personnel for IND/CTA preparations, meetings, and maintenance to support new and ongoing development programs. This role reports to the Senior Vice President, Regulatory Affairs.

This role can be hybrid out of the San Diego office or fully remote for a candidate based on the West Coast of the United States with some travel to the San Diego office.

Job Summary

Key Responsibilities:

  • Represent regulatory on study and program teams throughout study conduct and product development
  • Prepare and/or review regulatory documents required for global product development (e.g. New IND/CTAs, DSURs, IND Amendments, health authority meetings and briefing documents, iPSP/PIP, NDA/MAA)
  • Provide oversight of regulatory submissions vendor to assure technical accuracy, compliance, completeness, and timely regulatory agency submissions
  • Lead development of global regulatory submissions, including requests from regulatory authorities relating to clinical trials, and responses to health authority requests for information, as required
  • Manage and mentor direct reports to achieve department and corporate goals
  • Provide regulatory support for company compliance initiatives, including SOP development, and documentation initiatives, etc.
  • Review relevant clinical documents (protocol, informed consent form, investigator’s brochure, and site documentation, and required regulatory forms) for regulatory compliance
  • Keep current on US and OUS regulations that apply to company products and processes

Requirements

  • Bachelor’s degree required; advanced degree preferred
  • 12+ years of experience in pharmaceutical/biotech, with minimum of 10 years of experience in regulatory affairs including clinical regulatory affairs
  • Experience managing and mentoring direct reports
  • Experience with regulatory activities including creation of systems and processes to support efficient and high-quality submission of documents to regulatory bodies
  • Ability to translate regulatory requirements into practical achievable plans
  • Ability to build strong relationships with co-workers of various backgrounds and expertise
  • Demonstrated ability to achieve high performance goals and meet deadlines in a fast-paced environment
  • Strong organizational and multitasking skills
  • Excellent communication and interpersonal skills

Additional Information: This position requires interaction with various regulatory authorities and adherence to relevant procedures and regulations.

Benefits

We offer a competitive total compensation package and work in a supportive team environment. The anticipated salary range for candidates who will work in San Diego, CA, is $240,000 - $265,000 annually. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Contineum offers competitive compensation and benefits, including:

  • 90% employer-covered benefits
  • Flexible PTO
  • A very generous holiday schedule that includes a week off in August and time off around the winter holidays
  • A well-stocked kitchen with snacks and beverages
  • Additional benefits include the opportunity for annual bonuses, stock options, an Employee Stock Purchase Program, and a 401(k) with an employer match
  • The comprehensive wellness program includes medical, dental, vision, and LTD coverage

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FAQs About Senior Director, Regulatory Affairs Jobs at Contineum Therapeutics

What is the work location for this position at Contineum Therapeutics?
This job at Contineum Therapeutics is located in San Diego, CA, according to the details provided by the employer. Some roles may also include multiple work locations depending on the requirement.
What pay range can candidates expect for this role at Contineum Therapeutics?
Candidates can expect a pay range of $240,000 and $265,000 per year.
What employment applies to this position at Contineum Therapeutics?
Contineum Therapeutics lists this role as a Full-time position.
What experience level is required for this role at Contineum Therapeutics?
Contineum Therapeutics is looking for a candidate with "Executive" experience level.
Does Contineum Therapeutics allow remote work for this role?
Yes, this position at Contineum Therapeutics supports remote work, giving candidates the flexibility to work outside the primary office location.
What benefits are offered by Contineum Therapeutics for this role?
Contineum Therapeutics offers following benefits: Health Insurance, Dental Insurance, Vision Insurance, Disability Insurance, Paid Holidays, Flexible/Unlimited PTO, 401k Matching/Retirement Savings, and Health & Wellness Programs for this position. Actual benefits may vary depending on the employer's policies and employment terms.
What is the process to apply for this position at Contineum Therapeutics?
You can apply for this role at Contineum Therapeutics either through Sonara's automated application system, which helps you submit applications 10X faster with minimal effort, or by applying manually using the direct link on the job page.