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Associate Director, Healthcare Compliance

CytokineticsSouth San Francisco, California, United StatesOnsite

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.
We are seeking an Associate Director of Compliance to join our Compliance group.  This position will have the opportunity to provide compliance advice and support across the company, although based on experience and prior job responsibilities, this role will also have primary responsibility for defined functional areas.  This position will report to the VP, Chief Compliance Officer. This is an in-office role only.

Responsibilities


  • Serve as a key subject matter expert in supporting the compliance advisory needs of the organization
  • Expert understanding of the laws, regulations, industry standards, and guidelines for interactions with healthcare professionals and other Ethical codes and regulations
  • Advise on appropriate compliance interactions and policy guidelines, including on topics such as fair market value, advisory board participation, speaker programs, grants and corporate contributions
  • Lead the Compliance Auditing and Monitoring function, including building, conducting, and executing compliance audits or projects, and conducting in-person live monitoring of applicable areas (e.g., field rides)
  • Oversee and manage the process and capture of timely, accurate and consistent data for incorporation into filings and reports related to required HCP payment disclosure, including U.S. Sunshine Act and state law reporting
  • Partner with all Company internal clients to clarify and help validate data and prepare reports and filings for transparency data for final attestation by the Chief Compliance Officer
  • Oversee, manage, and engage in continuous improvement, review, drafting, and project management for all Compliance-specific policies, SOPs, guidelines, and work instructions
  • Manage and complete required compliance screening and other antibribery-anticorruption activities
  • Serve as an accountability partner for managing, maintaining, documenting, and dispatch of all Compliance-training materials, policies, or content (including New Hire Compliance Trainings) and other Learning Management System (LMS) project management areas
  • Oversee and manage the process, data capture, analytics, and report generation for compliance monitoring activities (live monitoring and process/documentation monitoring) in conjunction with the Chief Compliance Officer
  • Serve as principal Compliance reviewer for the Corporate Affairs Grant Review Committee (GRC), Independent Medical Education (IME) Review Committee, and other committees as may be assigned
  • Partner and collaborate, as appropriate and applicable, with Legal colleagues
  • Keep apprised of applicable federal, state, and local laws, industry codes and regulations and apply them to areas of responsibility
  • Experience with compliance auditing, monitoring, and compliance data systems, and privacy (CCPA and GDPR) helpful

Qualifications


  • Demonstrated expertise in pharmaceutical / life science & health law compliance is required. JD degree helpful but not required. Minimum of 7-10 years of experience in biotechnology, pharmaceutical, or life science related matters.
  • Detailed-oriented with a high level of intellectual, professional and interpersonal agility and flexibility.
  • Solution-oriented and growth mindset in working with clients on matters of compliance and ethics in the many emerging and novel areas of pharmaceutical/life science.
  • Excellent communication skills, both oral and written.
  • Well-organized and hardworking, with the ability to manage numerous projects simultaneously under deadline pressure.
  • Excellent analytical skills, with a strong ability to draft and review documents, analyze and provide compliance guidance, and apply policy guidance to business needs.
  • Ability to form strong working relationships with all levels of management, employees, and partners while maintaining firm adherence to proper ethical and compliance standards.
  • Team-oriented, sound judgment, self-motivation and willingness to take initiative. 

Actual salary at the time of hire may vary and may be above or below the range based on various factors, including, but not limited to, the candidate’s relevant qualifications, skills, and experience, as well as the service line and location where this position may be filled.Salary Pay Range$209,000 - $231,000USDOur employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered.

If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you.

Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.  


Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves.

Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers


Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process.Here are some ways to check for authenticity:

  • We do not conduct job interviews through non-standard text messaging applications
  • We will never request personal information such as banking details until after an official offer has been accepted and verified
  • We will never request that you purchase equipment or other items when interviewing or hiring
  • If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com

Please visit our website at: www.cytokinetics.com


Cytokinetics is an Equal Opportunity Employer



Life at Cytokinetics

We are a leading biopharmaceutical company focused on the discovery, development and commercialization of novel small molecule drugs that specifically target the cytoskeleton. The cytoskeleton is a complex biological infrastructure that plays a fundamental role within every human cell. A number of commonly used drugs and a growing body of research validate the role that the cytoskeleton plays in a wide array of human diseases. Our focus on the cytoskeleton enables us to develop novel and potentially safer and more effective classes of drugs directed at treatments for cancer, cardiovascular disease, fungal diseases and other diseases. We have developed a cell biology driven approach and proprietary technologies to evaluate the function of many interacting proteins in the complex environment of the intact human cell. We believe that our approach enhances the speed, efficiency and yield of our drug discovery and development process by accurately and rapidly identifying drug candidates with attractive properties. Our approach has yielded two drug candidates for the treatment of cancer, a drug candidate for the treatment of acute congestive heart failure and more than ten other research programs. Our most advanced drug candidate, SB-715992, is the subject of a broad Phase II clinical trials program designed to evaluate its effectiveness in many different types of cancer. An investigational new drug application, or IND, was filed with the U.S. Food and Drug Administration, or FDA, in 2003 for our second cancer drug candidate, SB-743921, which we expect will enter Phase I clinical development in early 2004. SB-715992 and SB-743921 are being developed through our strategic alliance with GlaxoSmithKline. In addition, we expect to initiate Phase I clinical development for a drug candidate, CK-1213296, for the treatment of acute congestive heart failure in the second half of 2004.
Thrive Here & What We Value1. Passionate about robust scientific thinking grounded in integrity and critical thinking2. Celebrates differences among employees3. Patient-centric approach to all actions and decisions4. Values integrity, ethics, doing the right thing, and being our best selves5. Emphasis on patient-centered care6. Focus on innovation and continuous improvement7. Dedicated to keeping the patient front and center in all actions and decisions8. Values-driven and sustainable approach to drug discovery and development9. Rigorous scientific thinking and critical thinking10. Emphasis on collaboration across different departments and teams
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