We are looking for our office based in Belgrade candidates for the position of Regulatory Officer 

Regulatory Officer (m/f)

Serbia, Belgrade

Responsibilities

Regulatory Officer is a member of the Regulatory and Safety Department that is primarily responsible to ensure successful compilation, submission, and maintenance of submissions/notifications to ethics committees and regulatory authorities in the frame of clinical studies, including safety reporting from clinical trials, in accordance with the applicable laws and regulations, as well as applicable Standard Operating Procedures (SOPs) and current Good Clinical Practice (GCP).

Regulatory Officer is responsible for set up and maintenance of a detailed overview of ethics and/or regulatory submission activities, including supplementary submission/notification status tracking of the approved studies in line with applicable regulations and ordinances.

Regulatory Officer is also responsible for review, preparation and negotiations of clinical trial agreements with health care institutions.

Education

University degree, preferably in Pharmacy or medical and life sciences.

Experience and knowledge

• Experience in clinical research within CRO and/or Biopharmaceutical environment is mandatory
• Knowledge of ICH GCP Guidelines as well as Ethics, Regulatory and Safety reporting requirements and relevant legislation both in the EU countries is preferred
• Strong interest in clinical research
• Fluent in local language and in English, both, written and verbal
• Computer proficiency is mandatory

Skills and personality

• Ability to read, analyze, and interpret common scientific and technical journals
• Excellent verbal and written communication skills
• Affinity to work effectively and efficiently in a matrix environment
• Very good interpersonal skills, attention to details and reasoning ability

By joining our fast growing and prosperous team, you will have a great opportunity for further personal growth and career development. We offer opportunity to work on the international projects and to be member of international clinical research teams, competitive compensation package, a lot of training opportunities and flexible working hours.

If you would be interested in joining Optimapharm team, please send your CV in in English and note that only shortlisted candidates that meet the requirements will be contacted for further selection process.

Deadline for applications: 14.02.2019.