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Senior Pharmacovigilance Scientist
2 months ago
We are seeking a highly skilled and experienced Senior Pharmacovigilance Scientist to join our team at GlaxoSmithKline. As a key member of our pharmacovigilance team, you will be responsible for ensuring the safe and effective use of our pharmaceutical products.
Key Responsibilities:- Design and implement pharmacovigilance strategies to identify and mitigate potential safety risks associated with our products.
- Collaborate with cross-functional teams to develop and implement risk management plans.
- Analyze and interpret safety data to inform product labeling and regulatory submissions.
- Develop and maintain relationships with regulatory agencies and industry partners.
- Stay up-to-date with emerging trends and best practices in pharmacovigilance.
- PhD or equivalent in a relevant field, such as pharmacology, toxicology, or epidemiology.
- Minimum 5 years of experience in pharmacovigilance, with a strong background in safety data analysis and risk management.
- Excellent communication and collaboration skills, with the ability to work effectively in a team environment.
- Strong analytical and problem-solving skills, with the ability to interpret complex data and develop effective solutions.
- Ability to work in a fast-paced environment and prioritize multiple tasks and projects.
- Experience with pharmacovigilance software and systems, such as Argus or Oracle.
- Knowledge of regulatory requirements and guidelines, such as ICH E2A and E2B.
- Experience with data analysis and statistical software, such as SAS or R.
- Ability to travel up to 20% of the time for meetings and training.
GSK is an equal opportunities employer and welcomes applications from all qualified candidates. We offer a competitive salary and benefits package, as well as opportunities for professional growth and development.
Please submit your application, including your CV and a cover letter, to [insert contact information]. We look forward to hearing from you
