Clinical Data Management Full-time Job

Clinical Data Management

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Job description Roles and Responsibilities • Writing drug trial methodologies (procedures) • Identifying and briefing appropriate trial investigators (clinicians) • Setting up and disbanding trial study centers • Designing trial materials and supplying study centers with sufficient quantities • Providing clinicians with instructions on how to conduct the trials • Collecting and authenticating data collection forms (commonly known as case report forms) • Monitoring progress throughout the duration of the trial • Writing reports

Desired Candidate Profile • Necessary to hold an undergraduate or postgraduate qualification in nursing, life sciences • (for example, biology, microbiology, toxicology, biochemistry, or pharmacology) or medical sciences (such as physiology, immunology, medicine, anatomy or pharmacy) • As of now recruiting only fresher’s Perks and Benefits Salaries will vary depending on the employer, specific job description, experience and qualifications. Role: Clinical research Scientist Industry Type: Clinical Research / Contract Research Functional Area Research & Development Employment Type: Full Time, Permanent Role Category Pharmaceutical & Biotechnology Education UG : MBBS in Any Specialization, B.Sc in Hospitality, Bio-Chemistry,

Interested to apply can share CV to info omasyresearch.com or for the zoom Screening Interview call/whatsapp to 9344064445.