Associate Director, Informed Consent

Are you passionate about ensuring ethical and compliant practices within the pharmaceutical industry? Do you have experience in informed consent and a strong understanding of regulations and guidelines? Bristol-Myers Squibb is seeking an Associate Director of Informed Consent to join our team and lead our efforts in this critical area. In this role, you will have the opportunity to make a direct impact on the lives of patients by ensuring their rights are protected during clinical trials. We are looking for a highly motivated individual with excellent communication skills and a strong attention to detail. If this sounds like you, we encourage you to apply and join our mission to discover, develop, and deliver innovative medicines to patients in need.

1. Develop and implement policies and procedures for informed consent to ensure compliance with regulations and guidelines in the pharmaceutical industry.
2. Monitor and assess the informed consent process for all clinical trials conducted by the company.
3. Train and educate staff on ethical and compliant practices related to informed consent.
4. Collaborate with cross-functional teams to ensure informed consent documents are accurate and reflect the needs of patients.
5. Oversee the review and approval of informed consent documents by regulatory bodies.
6. Conduct audits and risk assessments to identify and address potential issues related to informed consent.
7. Serve as a subject matter expert on informed consent for internal and external stakeholders.
8. Stay updated on changes in regulations and guidelines related to informed consent and make necessary updates to company policies and procedures.
9. Investigate and resolve any informed consent-related complaints or concerns.
10. Represent the company in discussions and negotiations with regulatory bodies on matters related to informed consent.
11. Provide guidance and support to clinical trial teams on informed consent-related matters.
12. Continuously evaluate and improve the informed consent process to ensure the rights of patients are protected.
13. Foster a culture of ethical and compliant practices within the company.
14. Collaborate with other departments, such as legal and compliance, to ensure informed consent processes align with company policies and regulations.
15. Participate in industry conferences and events to stay informed on best practices and advancements in the area of informed consent.

According to JobzMall, the average salary range for a Associate Director, Informed Consent in Princeton, NJ, USA is $100,000 to $150,000 per year. However, this can vary depending on the specific company, years of experience, and other factors.

Bristol-Myers Squibb Co. operates as a biopharmaceutical company, which engages in the discovery, development, licensing, manufacturing, marketing, distribution, and sale of biopharmaceutical products. It includes chemically-synthesized drugs or small molecules and products produced from biological processes called biologics.