Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Director, Compliance

$180k - $210k

Tonix Pharmaceuticals

Tonix Pharmaceuticals* is a fully integrated, commercial-stage biotechnology company focused on central nervous system (CNS) and immunology treatments in areas of high unmet medical need. TONMYA® (cyclobenzaprine HCl sublingual tablets 2.8 mg) is the first new treatment for fibromyalgia in adults in more than 15 years. Tonix’s CNS commercial infrastructure supports its marketed products, including its acute migraine products, Zembrace® Symtouch® (sumatriptan injection 3 mg) and Tosymra® (sumatriptan nasal spray 10 mg). Tonix is investigating TONMYA® in Phase 2 clinical trials to evaluate its potential in major depressive disorder and acute stress disorder/acute stress reaction. Tonix is also advancing a pipeline of immunology programs, including TNX-4800, a Phase 2 ready long-acting human anti-BorreliaOspA monoclonal antibody (mAb) for the prevention of Lyme disease in the U.S., and TNX-1500, a Phase 2 ready third-generation CD40 ligand inhibitor for the prevention of kidney transplant rejection. In addition, the Company is progressing TNX-2900 (intranasal potentiated oxytocin), which is Phase 2 ready for the treatment of Prader-Willi syndrome, a rare disease. To learn more, visit and follow the Company on LinkedIn and X.

*Tonix’s product development candidates are investigational new drugs or biologics; their efficacy and safety have not been established and have not been approved for any indication.*

Zembrace SymTouch and Tosymra are registered trademarks of Tonix Medicines. TONMYA is a registered trademark of Tonix Pharma Limited. All other marks are property of their respective owners.

Position Overview

The Director, Compliance reports to the VP, Legal & Compliance and supports the function in developing, implementing, and maintaining an effective Compliance Program that (1) supports and promotes a companywide culture of ethics and compliance, and (2) meets or exceeds applicable regulatory standards for effective compliance programs, including the Office of Inspector General (OIG) Guidance

Key Responsibilities
  • Provide strategic direction across all OIG seven elements of an effective compliance program leveraging knowledge of industry best practices
  • Assume primary responsibility for all healthcare compliance policies and educating business stakeholders in their application
  • Working collaboratively, draft, implement, administer and maintain relevant compliance policies, procedures, and work instructions
  • Management and oversight of 1) engagements with healthcare professionals and patients including FMV and 2) external funding (including sponsorships and grants) in collaboration with relevant stakeholders
  • Assist with designing and overseeing a comprehensive compliance monitoring program to assess adherence to internal policies, regulatory requirements, and industry standards. Lead risk-based monitoring activities across key business functions, including Commercial, Medical Affairs, and Market Access, to proactively identify and mitigate compliance risks. Develop actionable insights from monitoring outcomes, drive continuous improvement, and ensure timely reporting and remediation in collaboration with cross-functional stakeholders
  • Develop training plans and deliver effective compliance training programs to employees, enhancing awareness and understanding of ethical standards and legal obligations.
  • Lead the ongoing oversight of federal and state transparency reporting programs, including Open Payments (Sunshine Act) and state-specific disclosure requirements. Collaborate cross-functionally with Legal, Finance, Medical Affairs, and Commercial teams to build scalable processes that support transparency, mitigate risk, and promote ethical business practices.
  • Maintain a current working knowledge of various laws, regulations, and industry guidance that affect the compliance program, including antikickback and fraud and abuse laws, bribery and corruption, transparency laws, price reporting, OIG and DOJ guidelines, and industry standards, such as the PhRMA Code
Qualifications
  • MS, JD, MBA or other relevant advanced degree strongly preferred
  • 10+ years (with a B.S. degree), or 8+ years (with a graduate degree) of recent, relevant in-house experience in a compliance or related department of a healthcare organization or directly applicable law firm experience
  • Direct compliance experience in the pharmaceutical or medical device industry
  • Direct experience building programs and selecting and managing vendors
  • Direct experience leading significant programs and projects
  • Experience managing compliance programs, including drafting policies, developing and implementing training standards, leading monitoring initiatives, and conducting investigations on sensitive matters
  • Ability to apply a risk-based analysis to legal and compliance issues and develop creative and practical solutions that satisfy both business requirements and legal obligations
  • Ability to manage and drive the implementation of technical solutions (e.g., dashboards, portals) to manage processes including the HCP and patient engagement processes; monitoring; investigations workflows
  • Communicates complex compliance concepts effectively to the organization in a way that is connected to business objectives
  • Strong oral, written and presentation communication skills with superior attention to detail
  • Demonstrates initiative and excellent judgment; proactive; ability to work independently and collaboratively within a team setting; able to build relationships, both internally and externally
  • Demonstrated commitment to compliance, ethics, integrity, accountability and innovation

Salary Range

$180,000 - $210,000 USD

* Please note that Tonix does not offer sponsorship for this role.

Tonix provides a comprehensive compensation and benefits package which includes:

  • Medical, Dental & Vision Insurance, Basic and Voluntary Life and AD&D Insurance, Short- and Long-Term Disability Insurance, Flexible Spending Accounts, Health Savings Account, and Employee Assistance Programs
  • Pet Insurance
  • Retirement Savings 401k with company match and annual discretionary stock options
  • Generous Paid Time Off, Sick Time, & Paid Holidays
  • Career Development and Training

Tonix provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, genetics, or any other characteristic protected by law. In addition to federal law requirements, Tonix complies with applicable state and local laws governing nondiscrimination in employment. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfers, leaves of absence, compensation, and training. Tonix expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic, information, disability, veteran status, or any other characteristic protected by law.

#J-18808-Ljbffr
Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Director, Compliance in Berkeley Heights, NJ vacancy
  • $145k - $165k

     ...quality regulatory filings throughout the product lifecycle while ensuring compliance with U.S. FDA regulations and current guidance documents. Working in close collaboration with the Director of Regulatory Affairs, the Regulatory Affairs Manager serves as the... 
    Suggested
    Full time
    Flexible hours

    Breckenridge Pharmaceutical

    Berkeley Heights, NJ
    3 days ago
  •  ...Director, Healthcare Compliance The Director, Healthcare Compliance is responsible for leading and operating the Company's healthcare compliance program and promoting a culture of ethics, integrity, and compliance across the organization. Reporting to the Chief Legal... 
    Suggested
    Local area

    Aquestive Therapeutics

    Warren, NJ
    2 days ago
  • $90k - $125k

     ...commercial product lifecycle management, and providing backup to the Director of Regulatory Affairs. The role plays an essential part in...  ...(CBE/PAS), annual reports, and labeling supplements in compliance with FDA requirements. Author relevant eCTD sections using... 
    Suggested
    Full time
    Flexible hours

    Breckenridge Pharmaceutical

    Berkeley Heights, NJ
    2 days ago
  •  ...An innovative commercial-stage biotechnology company is seeking a Senior Regulatory Affairs Specialist to support regulatory compliance and submission activities across both marketed products and development-stage programs. This individual will contribute to regulatory... 
    Suggested

    EPM Scientific

    Summit, NJ
    4 hours ago
  •  ...Compliance Specialist, Equipment Commissioning & QualificationThe Compliance Specialist, Equipment Commissioning & Qualification, supports the successful operation of facility, laboratory, and business functions at multi-use sites through interaction with internal team... 
    Suggested
    Work at office
    Local area

    Omni Inclusive

    Summit, NJ
    2 days ago
  • $70k - $150k

     ...Associate Manager, Financial InvestigationsKroll's North American Investigations, Diligence and Compliance - Specialist practice is seeking an Associate Manager based in the U.S. This is a wide-ranging role in the Financial Investigations team. The Associate Manager will... 
    Temporary work
    Interim role
    Flexible hours

    Kroll

    Morristown, NJ
    1 day ago
  • $166.72k - $250.08k

     ...Associate Director, Regulatory Affairs Advertising and Promotion Job Requisition ID: 1826 Posting Start Date: 7/16...  ...recommendations for branded and unbranded promotional materials to ensure compliance with FDA advertising and promotion requirements, approved... 
    Work at office

    Daiichi Sankyo, Inc.

    Basking Ridge, NJ
    2 days ago
  • $173.2k - $272.6k

     ...Job Description Tech Solutions Product Compliance & Sustainability Global Lead- Role Purpose: - The Product Compliance position leads the global Product and Environmental Compliance function across our company AHTS's product portfolio, covering both electronic... 
    Full time
    For contractors
    Local area
    Relocation
    Visa sponsorship
    Flexible hours
    Shift work

    Merck & Co.

    Rahway, NJ
    6 days ago
  • $187.7k - $227.45k

     ...Bristol Myers Squibb seeks a Director of Quality Compliance for its Cell Therapy manufacturing facility in Summit, New Jersey. This leader will develop and oversee site compliance programs, manage regulatory inspections, conduct internal audits, and ensure adherence to... 

    Bristol Myers Squibb

    Summit, NJ
    8 days ago
  • $182k - $346k

     ...Director Regulatory Affairs Global Regulatory Lead (GRL II), Global Regulatory Strategy (Neuroscience) AbbVie's mission is to discover...  ...anticipates and mitigates regulatory risks. Ensures compliance with global regulatory requirements. Manages compounds through... 
    Work at office
    Immediate start
    Remote work
    Worldwide
    Monday to Friday

    AbbVie

    Florham Park, NJ
    3 days ago
  • $100k - $150k

     ...excellence The Company is an equal employment opportunity employer. #LI-AV1 #LI-HYBRID Responsibilities As our Regulatory Compliance Manager , you'll report to the operating unit General Counsel and be responsible for designing, executing and overseeing... 
    Full time
    Work at office
    Remote work

    Berkley

    Morristown, NJ
    5 days ago
  • $190k - $230k

     ...and QA manufacturing processes from CMC RA perspective, tracking of Heath Authority commitments, leading global submissions and compliance to global regulations. Responsible for drafting, authoring, reviewing, and submitting key regulatory documents including Investigational... 
    Contract work
    Work experience placement
    Work at office
    3 days per week

    DBV Technologies

    Warren, NJ
    20 hours ago
  • $120k - $145k

     ...world. About the Role This position reports to the Vice President, Quality Assurance and will manage or support: cGMP compliance assessment of contract manufacturers, the company SOP and Training systems, QA/QC Testing /Audit program, and Quality/Compliance... 
    Full time
    Contract work
    Flexible hours

    Breckenridge Pharmaceutical

    Berkeley Heights, NJ
    16 hours ago
  •  ...Associate Director role supporting a Microsoft Power Platform-based regulatory requirements management system within Global Regulatory...  ...and permission management Experience with software development lifecycle practices and regulatory or GxP compliance documentation... 

    Merck

    Rahway, NJ
    8 days ago
  • $129k - $203.1k

     ...with mutual respect and shared accountability. The Associate Director, Regulatory Affairs - Power Platform Solutions Specialist is...  ...or Enterprise IT as appropriate. Technical Documentation, Compliance & Engineering Quality Create and maintain accurate technical... 
    Full time
    For contractors
    Local area
    Relocation
    Visa sponsorship
    Flexible hours
    Shift work

    Merck & Co.

    Rahway, NJ
    13 days ago
  •  ...Associate Director leading regulatory strategy for oncology advertising and promotion at AbbVie. Oversees cross-functional teams, manages departmental operations, and develops complex regulatory initiatives with minimal direction. Based in one of four US headquarters... 

    AbbVie

    Florham Park, NJ
    8 days ago
  • Responsibilities: US Agent for all products, responsible for communication between the FDA and manufacturing sites. Communicate and follow-up status with FDA for any Chemistry, Bioequivalence and Patents issues and correspondences on both pending and approved...
    Local area

    Katalyst Healthcares and Life Sciences

    Madison, NJ
    16 hours ago
  •  ...reports and renewals across assigned regions.Responsible for appropriate entering and quality of product specific attributes in compliance database.Ensures regulatory compliance for project and keeps records of all major HA interactions in the validated document management... 
    Immediate start
    Worldwide

    Artech

    East Hanover, NJ
    16 hours ago
  • Regulatory Affairs Specialist Job Type: Full time - Permanent Location: Madison, New Jersey (On-site) A commercial-stage transplant technology company, part of a global medtech group, is changing how donor organs are preserved and assessed before transplant. Their...
    Permanent employment
    Full time

    Skills Alliance

    Madison, NJ
    2 days ago
  • About the Role: VDA is seeking a highly organized and detail-oriented Corporate Compliance Coordinator to oversee the administration, maintenance, and renewal of the company's business licenses, registrations, permits, and related compliance filings across multiple jurisdictions... 
    Work at office
    Local area

    VDA

    East Hanover, NJ
    1 day ago
  •  ...Role: QA Director Location: Omaha, NE, Berkeley Heights, NJ (100% Onsite - local only no relocation) Full Time What You Will Do: Manage and coach 4 direct reports and 36 indirect reports. Drive Quality Practices and Standards across the Organization... 
    Full time
    Local area
    Relocation

    Veracity

    Berkeley Heights, NJ
    16 hours ago
  •  ...AbbVie seeks a Director of Global Regulatory Strategy for its neuroscience portfolio in Florham Park, NJ. This senior regulatory role...  ...pharmaceutical products through all development phases while ensuring compliance with worldwide regulatory requirements. Responsibilities... 
    Worldwide

    AbbVie

    Florham Park, NJ
    8 days ago
  • $180k - $195k

     ...Director Of Financial Planning & Analysis Green Street is seeking a high-caliber Director of Financial Planning & Analysis to join...  ...and maintain all debt and financing models including covenant compliance schedules, interest expense forecasts, SOFR / benchmark rate updates... 
    Full time
    Work experience placement
    Visa sponsorship
    Work visa

    Green Street Advisors

    Summit, NJ
    2 days ago
  • $193.04k - $289.56k

    At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in...

    Daiichi Sankyo, Inc.

    Basking Ridge, NJ
    1 day ago
  • Stable project pipeline Opportunity to grow with a well known General Contractor About Our Client Our client is a leading general contractor with a specialized focus on healthcare construction . With experience delivering on hospitals, surgical centers,...
    For contractors
    For subcontractor
    Work at office
    Local area

    Michael Page International Inc.

    Summit, NJ
    1 day ago
  •  ...partnership with a leading provider in the insurance industry is seeking a Sr. GRC Analyst that will establish governance, risk, compliance, vendor risk, and vulnerability management activities with increasing independence. This role is designed for a developing risk professional... 

    Optomi

    Short Hills, NJ
    2 days ago
  • $100k

     ...DoD SkillBridge Internship: Executive Director SkillBridge Industry Mentor Job Information Business Clients Name: Juniper Communities...  ...and local regulatory standards. Responsibilities Ensure compliance to Juniper Communities' philosophy and hallmarks as well as... 
    Internship
    Local area
    All shifts

    Vets2PM

    Chatham, NJ
    1 day ago
  • $157.6k - $205.43k

    About Axtria – Introduction Axtria is a global data analytics and commercial solutions company focused on life sciences. We work with leading pharmaceutical and healthcare organizations to help them use data, analytics, technology, and AI to make better business decisions...
    Hourly pay
    Full time
    Work at office
    Relocation
    Flexible hours

    Axtria - Ingenious Insights

    Berkeley Heights, NJ
    1 day ago
  •  ...related to raw materials, including flavors, fragrances, and cosmetic ingredients. This role involves interpreting and maintaining compliance with global regulations, managing documentation, and collaborating with internal and external partners to ensure regulatory... 

    ClinLab Solutions Group

    Middlesex, NJ
    5 days ago
  • QA Lead Location: Berkeley Heights, NJ (Onsite) Type: Contract (Automation, Selenium, Mobile, Web Testing) Analyze Business Requirements Documents to get better understanding of the system both on technical and business perspectives. Postman, Pipeline testing ...
    Contract work

    InterSources

    Berkeley Heights, NJ
    2 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Director, Compliance. Be the first to apply!