Scientist, Protocol Design and Development Specialist

3 weeks ago


Belfast, United Kingdom Celerion Full time
Celerion is a leading clinical research organization committed to delivering exceptional results through innovative research strategies. We are seeking a highly skilled Scientist, Protocol Design and Development to join our Clinical Pharmacology team. This role involves developing protocols that incorporate proper study design based on scientific research and regulatory requirements. Key responsibilities include developing protocol designs, collaborating with cross-functional teams, and ensuring compliance with regulatory guidelines. The ideal candidate will possess a strong background in science, excellent communication skills, and experience in the pharmaceutical industry. If you are a motivated and detail-oriented professional looking to contribute to a dynamic team, we encourage you to apply.
Requirements:
  • Minimum of Bachelor's degree in a science-related field
  • Medical professional (PharmD, RN, etc.) preferred
  • Knowledge of study design, pharmacology, and pharmacokinetics is an asset
  • 0-2 years of experience in the pharmaceutical industry or related field required (recent MSc or higher graduates will be considered)
  • Knowledge of GCP, GLP, FDA, EMEA, TPD, and ICH guidelines and regulations is an asset
  • Excellent oral and written communication skills
  • Salary will be based on experience and an attractive benefits package is provided

Celerion Values: Integrity Trust Teamwork Respect
Celerion is an Equal Opportunity Employer.
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