The ideal candidate will have patient-facing experience and at least 1 year of experience as a study coordinator in a clinical trial setting. Phlebotomy training/experience, laboratory sample processing experience, and ECG training are strongly preferred.
Responsibilities:
Qualifications:
About the job Principal Medical Writer - Regulatory and Medical WritingJob Title: Principal Medical Writer - Regulatory and Medical WritingJob Location: Carlsbad, CA, USAJob Location Type: RemoteJob Contract Type: Full-timeJob Seniority Level: Mid-Senior level...
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