Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Celerion offers one of the most experienced clinical pharmacology research networks in the industry.

Are you looking for an opportunity to support a business creating life-saving treatments? If so, we cant wait to meet you!

Celerion is seeking a Scientist, Protocol Design and Development to join our Clinical Pharmacology team. This role is responsible for the development of protocols incorporating proper study design based upon scientific research and regulatory requirements as well as being responsible for the development of protocol designs as required.

Requirements:

• Minimum of Bachelors degree in science related field required
• Medical professional (PharmD, RN etc) preferred
• Knowledge of study design, pharmacology, and pharmacokinetics will be considered an asset
• 0-2 years 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 will be considered an asset
• Excellent oral and written communication skills
• Salary will be based on experience and an attractive benefits package is provided. This role will be based at our Belfast, Northern Ireland site
  
  

Celerion Values: Integrity Trust Teamwork Respect

Celerion is an Equal Opportunity Employer.