A constantly growing International CRO with an increasing pipeline of new projects and internal promotions they are now seeking a Senior Drug Safety professional to be part of thier success.

You will will be involved in managing individual case reports (SAEs, ADRs), reconciliation of SAEs, coding and data retrievals from the safety database, supporting the generation of periodic safety reports, and DSMB/DMC reviews. You will be involved in the safety management team and interfacing with the client and project team. You will also participate in responsibilities which range from signal generation activities to being responsible for ensuring relevant case reconciliation; Provision of line listings and tabulations for safety reports i.e. periodic safety reports, ad hoc safety reports etc.

Qualifications

An educational background in life sciences will be essential with the addition of having worked in a similar role, with an understanding of regulations relevant to the safety of drugs in development and post authorizations, as well as knowledge of clinical research.
Ideally you have experience in effectively coaching and mentoring less experienced safety associates. Fluency in English is required and German is a plus.

If you would to discuss this role in greater detail or your application / suitability to this or further roles, please call me or email me in confidence. If you are not available or suited to this position, please feel free to pass my details on.

SEC Pharma People are acting as an Agency and or Employment Business
For a confidential consultation call Manpreet Mangat on 0044 (0) 207 255 6600 or email your CV to
manpreet.mangat@SECpharma.com

SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business