Clinical Research Scientist

• This position has a key role to assist the global clinical development, regulatory, and safety to continually assess and analyze clinical safety signal data and inform key stakeholders to implement strategies to minimize risk and proactively partner with global health authorities.
• This position includes interactions with all areas within clinical development, medical affairs, independent review committees, and regulatory authorities to ensure timely identification, reporting, and response to health authorities with regards to safety issues.

• Minimum 2 yrs. experience in medical or technical writing
• Clinical monitoring experience preferred
• Extensive medical/scientific and clinical research knowledge
• Knowledge of Medical Terminology
• Knowledge of clinical trial design, basic statistics, pharmacodynamics and pharmacokinetics proficient at data review and interpretation
• Experience in all aspects of the drug development process
• Knowledge of GCP and ICH Guidelines
• Proficient in Microsoft Word, Excel, PowerPoint; EDC databases, SAS datasets

All your information will be kept confidential according to EEO guidelines.

IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 646-618-8925 ASAP! I want to know more about your preferences.

If in case you know someone who might be interested for this, feel free to pass it along. I look forward to hearing from you!