Offer summary

Qualifications:

Bachelor's degree in life sciences or related field., Minimum of 5 years of experience in clinical research., Strong knowledge of GCP and regulatory requirements., Excellent communication and organizational skills..

Key responsibilities:

Oversee clinical trial operations and ensure compliance with protocols.

Coordinate with investigators and site staff to facilitate study activities.

Prepare and review study documentation and reports.

Monitor data collection and ensure accuracy and integrity of data.

Emerald Clinical is a leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence. With over 20 years of experience and more than 500 people managing 40 geographical locations throughout the Asia-Pacific region, USA and Europe, Emerald Clinical provides the full range of clinical trial services to biopharmaceutical, medical device, and diagnostic customers, for all trial phases, registration, and post-marketing trials.Stay up to date on the latest clinical research news, case studies and perspectives from Emerald Clinical thought leaders by signing up for our monthly e-newsletter.emeraldclinical.com/subscribe/newsletter

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