Responsibilities
1.Extensive experience in clinical development and the pharmaceutical industry preferably with at least 3 years in Quality Assurance/ Compliance roles.
2.Thorough and extensive knowledge of international GCP regulations including FDA/EU GCP, ICH, pharmacovigilance, new drug regulations, other key HA guidance?s, and current industry practice
3.Excellent verbal and written communication skills/ computer skills
4.Excellent problem solving and decision making skills. Skilled at conflict resolution / negotiation.
5.Capable of working independently as well as part of a cross-functional team demonstrating the ability to influence and create alignment across multiple functional areas.
6.Flexibility to react to changing priorities in a dynamic business environment
Only Candidates from EU counties will be considered due to restrictive work permit policy.
Please send your CV to beata.klecz@secpharma.com or call on 00442072556665