Cardio Safety Scientist
We are seeking a highly motivated STUDY DIRECTOR in CARDIOSAFETY PHARMACOLOGY STUDIES with a preferable experience in cellular patch-clamp assays to join our Safety Assessment Department located in Evotec Verona (Italy).
We are looking for professionals with these required skills to achieve our goals:
Key Responsibilities
- Act as Study Director responsible for the conduct of in-vitro safety pharmacology studies (GLP).
- Career development opportunities in the management of cardiovascular telemetry studies.
- Responsible for the planning, co-ordination, reporting and archiving of studies.
- Ensuring the delivery of high quality data within agreed timelines to meet clients expectations.
- Conduct safety assessment work in accordance with the appropriate guidelines (ICH, OECD, EMA, FDA, CIPA. )
and regulations (GLP).
- Contribute to setting up and validating new equipment/software and assays as needed.
- Establish and maintain strong working relationships with clients.
Qualifications Required:
- Minimum of a Bachelor's Degree, Master's Degree in pharmacology, or a closely related field of study;
Experience Required:
- Proved experience as electrophysiologist in manual patch-clamp assays in whole cell configuration.
- Technical writing proficiency
- Direct experience with Good Laboratory Practices.
General Qualifications:
- Collaboration & Teamwork: Relates to employees and management in a cooperative manner that helps others to achieve their best.
- Productivity/Organizing/Planning: Meets deadlines, demonstrates effective use of time, and handles multiple assignments simultaneously.
- Communication Skills: The ability to convey both written and verbal information effectively and efficiently.
- MS Office.
- Detail-Oriented: Follows precise procedures and demonstrates thoroughness in performing job tasks and assignments.
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