Senior Manager, Pharmacovigilance Science
Welcome to Bristol-Myers Squibb, a global biopharmaceutical company committed to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. We are seeking a highly qualified and experienced Senior Manager of Pharmacovigilance Science to join our dynamic team.In this role, you will be responsible for leading a team of pharmacovigilance scientists in the evaluation and monitoring of safety information for our products. Your expertise and leadership will be critical in ensuring compliance with global pharmacovigilance regulations and guidelines, as well as driving the continuous improvement of our pharmacovigilance processes.To be successful in this role, you must have a strong scientific background and extensive experience in pharmacovigilance, as well as proven leadership skills. Additionally, you should possess excellent communication and problem-solving abilities, as well as the ability to collaborate effectively with cross-functional teams.If you are passionate about making a meaningful impact in the lives of patients and have the qualifications we are looking for, we invite you to apply for this exciting opportunity with Bristol-Myers Squibb.
Lead a team of pharmacovigilance scientists in the evaluation and monitoring of safety information for company products.
Ensure compliance with global pharmacovigilance regulations and guidelines.
Drive continuous improvement of pharmacovigilance processes.
Utilize strong scientific background and extensive pharmacovigilance experience to guide decision-making and problem-solving.
Provide leadership and guidance to team members, fostering a collaborative and productive work environment.
Communicate effectively with cross-functional teams, including medical, regulatory, and commercial teams.
Conduct regular reviews and analysis of safety data to identify potential risks and trends.
Develop and maintain strong relationships with external stakeholders, such as regulatory agencies and business partners.
Stay updated on industry trends and regulations related to pharmacovigilance and incorporate changes into company processes and procedures.
Participate in the planning and execution of clinical trials to ensure proper safety monitoring.
Prepare and present reports on pharmacovigilance activities to senior management and other relevant stakeholders.
Mentor and coach team members to promote their professional growth and development.
Collaborate with internal and external stakeholders to ensure timely and accurate reporting of adverse events.
Work closely with other departments, such as medical affairs and regulatory affairs, to ensure alignment and integration of safety information.
Support the company's commitment to patient safety and positively impact the lives of patients by ensuring the safe use of company products.
Bristol-Myers Squibb is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
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Lead a team of pharmacovigilance scientists in the evaluation and monitoring of safety information for company products.
Ensure compliance with global pharmacovigilance regulations and guidelines.
Drive continuous improvement of pharmacovigilance processes.
Utilize strong scientific background and extensive pharmacovigilance experience to guide decision-making and problem-solving.
Provide leadership and guidance to team members, fostering a collaborative and productive work environment.
Communicate effectively with cross-functional teams, including medical, regulatory, and commercial teams.
Conduct regular reviews and analysis of safety data to identify potential risks and trends.
Develop and maintain strong relationships with external stakeholders, such as regulatory agencies and business partners.
Stay updated on industry trends and regulations related to pharmacovigilance and incorporate changes into company processes and procedures.
Participate in the planning and execution of clinical trials to ensure proper safety monitoring.
Prepare and present reports on pharmacovigilance activities to senior management and other relevant stakeholders.
Mentor and coach team members to promote their professional growth and development.
Collaborate with internal and external stakeholders to ensure timely and accurate reporting of adverse events.
Work closely with other departments, such as medical affairs and regulatory affairs, to ensure alignment and integration of safety information.
Support the company's commitment to patient safety and positively impact the lives of patients by ensuring the safe use of company products.
Bristol-Myers Squibb is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Apply tot his job
Apply To this Job