Scientist, Protocol Design and Development
|Title:||Scientist, Protocol Design and Development|
|Department:||Data Management and Biometrics|
|Location:||Lincoln NE or Montreal Canada|
Due to the expansion of our Clinical Pharmacology team, Celerion is seeking a Scientist, Protocol Design and Development. 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.
Skill and educational requirements include:
- Minimum of Bachelor's 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 Montreal, Quebec or Lincoln, Nebraska site.
This opening is closed and is no longer accepting applications
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We are an equal opportunity employer
Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, genetic information, marital status, qualified protected veteran status, or disability.