Live opening · Posted 7 days ago
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Description supplied by the original job listing.
To build all necessary data/information needed to prepare internal documents/scientific reports related to clinical trials by assisting with ongoing blinded efficacy and safety reviews.
Responsibilities
Prepare scientific reports and presentations related to clinical trials using available software and templates.
Assists in constructing phase 1 clinical study planning documents, and writes Phase 1 protocols.
Comply with procedures set forth in relevant IQS documents and Study protocols
Comply with the directives issued by the management regarding clinical studies.
Commit to producing work of the highest quality
Pay close attention to detail
Perform literature and competitive intelligence searches
Apply experience to analyze clinical study data, using available software to assist with ongoing blinded/un-blinded pharmacokinetic analysis
Responsible for receiving and completing assignments and tasks from functional Scientific Staff or Therapeutic Area MD within a given time period with supervision.
Bachelor’s degree, in Science, related to Field with +2 years’ experience in pharmaceutical industry. Or Masters degree in pharmacology or related field.
Associates degree/RN with 6+ years of experience in pharmaceutical industry may be additionally considered.
Must possess good oral and written communication skills
Ability to use computer to generate reports, analyze data, and create presentations
Previous experience may be narrowly-focused or limited.
Ability to identify opportunities and participate in process improvement initiatives.
Employment type
Full-time
Work arrangement
Hybrid
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