Pharmacovigilance Lead
- Employer
- Simbec-Orion
- Location
- Slough, United Kingdom
- Salary
- Competitive
- Start date
- 15 Apr 2021
- Closing date
- 1 May 2021
View more
- Discipline
- Clinical Research, Pharmacovigilance
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
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Job Details
Simbec-Orion is a responsive and agile full-service CRO, with wide therapeutic experience and specialist expertise in clinical pharmacology, oncology and rare diseases. Perfectly structured, we provide full-service clinical development solutions for small and mid-size drug developers - headed up by a centralised leadership team.
With a focus on tailormade and scalable solutions, we'll adapt our delivery style, communications and operations to suit the demands of your project, helping you achieve your clinical and commercial objectives. Because our goal is the same as yours; to improve patients' lives.
Main Duties and Responsibilities:
We are looking for a Pharmacovigilance Lead to join our Pharmacovigilance department.
You will act as the primary point of contact for external clients on a range of studies/projects to provide a high level of service to our clients by ensuring deliverables are executed to high standards on time and in line with the contractual agreement.
You will carry out PV tasks on studies/projects and be involved in training/mentoring PV team members. You will work with the Senior PV Manager or Head of Department to address any project concerns and assist with audits/inspections.
Minimum Requirements:
Essential:
Desirable:
Simbec-Orion is an equal opportunity employer. Simbec-Orion will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law.
With a focus on tailormade and scalable solutions, we'll adapt our delivery style, communications and operations to suit the demands of your project, helping you achieve your clinical and commercial objectives. Because our goal is the same as yours; to improve patients' lives.
Main Duties and Responsibilities:
We are looking for a Pharmacovigilance Lead to join our Pharmacovigilance department.
You will act as the primary point of contact for external clients on a range of studies/projects to provide a high level of service to our clients by ensuring deliverables are executed to high standards on time and in line with the contractual agreement.
You will carry out PV tasks on studies/projects and be involved in training/mentoring PV team members. You will work with the Senior PV Manager or Head of Department to address any project concerns and assist with audits/inspections.
Minimum Requirements:
Essential:
- BSc Life Sciences Degree
- Demonstrable experience in Pharmacovigilance case processing, quality reviewing of ICSRs and database reconciliation
- Previous experience in Pharmacovigilance Project Management
- Previous experience in a Clinical Research Organisation
- Demonstrated experience in all aspects of Developmental and Postmarketing Pharmacovigilance.
Desirable:
- MSc Life Sciences or overseas equivalent
- PhD in Life Sciences
- Pharmacy degree Experience in Business Development activities.
Simbec-Orion is an equal opportunity employer. Simbec-Orion will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law.
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