Hiring for Mbbs, MD (Any Discipline) - With or Without Clinical Experience in Mysore, for Exp. 0 - 5 yrs at Boiclinica India Pvt Ltd.

  • Esteemed client of Orion TrueTech Services India
  • Mysore, Karnataka, India
  • Apr 11, 2018
Full time Pharma, Healthcare & Biotechnology Jobs

Job Description

Job Description:Are you an qualified MBBS / MD? Do you want to do something NEW? DIFFERENT? INNOVATIVE? INTERESTING? LUCRATIVE? Are you interested in a Corporate Career? Are you interested in a POPULAR &amp amp amp STABLE Industry related to Medicine?&amp amp nbsp WE ARE HIRING MBBS, MD CANDIDATES WITH OR WITHOUT ANY EXPERIENCE Top reasons you should join us: Build purpose . Our work improves lives. Bioclinica has helped pharmaceutical and biotech companies over the last 30+ years to develop drugs and its safety in the marketplace today. You will personally contribute every day to advancing healthcare and make a better place to live. Brilliant people . We are building a team of Strategic professionals, Business Relationship Managers, and hiring new Safety professionals to innovate &amp amp amp transform Drug Safety unit at Bioclinica. You will learn with the most talented group of individuals, in an agile, supportive, and caring environment. Bright potential. You will work on the most stimulating and challenging cases, in a flexible work environment, with the training and career development that will help you thrive personally and professionally. We are expanding in a big way and there is no better time to join Bioclinica India. Lets together shape the future and new possibilities for your career and improve the lives of patients around the world. Visit www.bioclinica.com JOB TITLE: Drug Safety Physician (Medical Reviewer) LOCATION: Mysore YEARS OF EXPERIENCE: ANY / NO EXP REQUIRED EDUCATION: MBBS/MD (in any discipline) ESSENTIAL DUTIES AND RESPONSIBILITIES:&amp amp nbsp As a Medical Reviewer Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regulatory report ability of cases obtained from clinical trials, spontaneous and solicited reports within assigned therapeutic team and across all products/sites, as necessary, and in a timely fashion Determine seriousness and relatedness across products as assigned Review and verify appropriate selection of adverse events from source documents, assign appropriate MedDRA code, assess labeling, review narrative. Acquire and maintain current knowledge of product portfolio and safety profiles for products across therapeutic areas Escalate complex case issues on client product(s) to the medical review team of the client as appropriate Identify and resolve case issues, coordinate with client therapeutic teams/site for specific products or functional groups Communicate and interact effectively within and across all client therapeutic teams, and within functional team management as appropriate Acquire and maintain knowledge of applicable Global Health Authority regulations Perform any other drug safety related activities as assigned Participate in internal and external audits and inspections by clients and health authorities SPECIALIZED KNOWLEDGE AND SKILLS: Experience with relevant safety databases and related software applications Proven experience in customer handling and relationship. Proven ability to perform task management. Must have good presentation skills and the ability to give presentations.&amp amp nbsp Knowledge of the Life Sciences Industry and life cycle of drug. Relevant product and industry knowledge.