Senior Manager, Regulatory Affairs
- Company
- CK Clinical
- Location
- Basel
- Salary
- up to 77 CHF per hour(self-empl)
- Posted
- 02 Feb 2021
- Closes
- 26 Feb 2021
- Ref
- 49796
- Contact
- Jocelyn Blackham
- Discipline
- Medical Affairs
- Hours
- Full Time
- Contract Type
- Contract
- Experience Level
- Experienced (non-manager)
Jocelyn Blackham is recruiting for a Senior Manager within Regulatory Affairs to join a company in the leading pharmaceutical company at their site based in Basel on a contract basis for 6 months, with the possibility of extension.
The main purpose of the role will be to:
- Provide strategic and operational regulatory direction and support global program team for programs through development, registration and approval/post approval.
- Regulatory strategy and managing operational activities for assigned regions.
- Determine requirements and sets objectives for Health Authority (HA) interactions with relevant representative.
- Lead HA meetings independently or with relevant representative.
Further responsibilities will include:
- Partnering with regions to align on regulatory strategy in order to fulfil business objectives.
- Working closely with regulatory consultants/advisors for global strategic input and challenge.
- Identifying issues, gaps, and trade-offs affecting optimal and timely submission and approval.
In order to be considered for this role, you will be required to have the following qualifications, skills and experience:
- Previous experience within a relevant role.
- Heavily involved in strategy in a previous role.
- Relevant qualifications within a Life Science discipline.
- Experience interacting and ideally meetings HA meetings.
This is an excellent opportunity to join a global pharmaceutical company.
Please could you send any correspondence in English. Please quote reference 49796 in all correspondence.
The main purpose of the role will be to:
- Provide strategic and operational regulatory direction and support global program team for programs through development, registration and approval/post approval.
- Regulatory strategy and managing operational activities for assigned regions.
- Determine requirements and sets objectives for Health Authority (HA) interactions with relevant representative.
- Lead HA meetings independently or with relevant representative.
Further responsibilities will include:
- Partnering with regions to align on regulatory strategy in order to fulfil business objectives.
- Working closely with regulatory consultants/advisors for global strategic input and challenge.
- Identifying issues, gaps, and trade-offs affecting optimal and timely submission and approval.
In order to be considered for this role, you will be required to have the following qualifications, skills and experience:
- Previous experience within a relevant role.
- Heavily involved in strategy in a previous role.
- Relevant qualifications within a Life Science discipline.
- Experience interacting and ideally meetings HA meetings.
This is an excellent opportunity to join a global pharmaceutical company.
Please could you send any correspondence in English. Please quote reference 49796 in all correspondence.