Sharon Syme
Regulatory Affairs Assistant@ Merck Life Science
Livingston, Scotland, United Kingdom
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Sharon Syme is a highly experienced Regulatory/Quality Compliance officer with 9.2 years of work experience. She has a strong background in clinical research, medical devices, and clinical trials. Sharon has worked in various roles, including Regulatory Affairs Assistant at MERCK and Clinical Trial Administrator at ETHICON. She is skilled in clinical development, good clinical practice, and clinical trial management systems. Sharon has also worked at IQVIA and IQVIA in different countries. She is currently based in Livingston, Scotland.
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Emails and Phone Numbers

@merckgroup.com
@davesinclair.com
@kinly.com
+49 180032****
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About

Currently working as a Regulatory/Quality Compliance officer, for a small start-up company. I have been a Regulatory Affairs Assistant at MERCK within the Medical Device/Life Science sector. I have also been a Clinical Trial Administrator at ETHICON (Johnson & Johnson) and a Clinical Project Co-ordinator with Quintiles (IQVIA) therapeutic studies (medical device trials).

Work Experience

Frankfurter Straße 250, Darmstadt, 64293, DE

Biotechnology Research

7758
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Sharon Syme's Professional Milestones

  • Clinical Trial Administrator (2016-04-01~2019-02-01): Successfully executed comprehensive clinical trials, optimizing patient outcomes and fostering a positive healthcare environment.
  • Clinical Project COOrdinator (2014-08-01~2016-01-01): Successfully delivered multiple clinical projects on time and within budget, delivering exceptional results on time and within budget.
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