Promote good clinical practices in the conduct of clinical investigations by possessing an in-depth knowledge of federal regulations and K2 Medical Research guidelines (SOPs) for the enrollment and maintenance of subjects in clinical trials, and by collecting, recording, and maintaining source and sponsor documentation. Job DescriptionJob Description
At K2 Medical Research, we are transforming healthcare by delivering tomorrow’s treatments today.
· 4+ years of experience within a services organization, ideally a pharmaceutical, biotechnology, or contract research organization.
· 6+ years of experience leading teams and managing complex, cross-functional projects.
· Strong analytical and critical thinking skills with a track record of sound judgment in fast-paced, deadline-driven environments.
· Proven leadership capability with a coaching mindset and a consistently collaborative, supportive approach to developing others.
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- Drug Development Strategy: Provides input to the clinical development plan to ensure the overall strategy can deliver the pre-specified product profile, is logical, scientifically sound, proposed studies have appropriate designs, efficacy and safety information to be collected meet regulatory agencies’ requirements for countries and regions the drug is to be submitted.