Clinical Project Specialist ( Clinical Trial ) / Up $4 K

Responsibilities

• To support clinical study(ies) are run to time and budget and are completed in compliance with all
• relevant laws, regulations, and regulatory guidelines
• To participate as a Global Clinical Trial Representative in cross-functional teams such as Case Report Form Review Team and Clinical Trial Team.
• To assist on regional study feasibility, the initial assessment of any vendors, supplies planning and the development of study specific documents and timelines as required.
• To assist on region-specific document development including the informed consent forms;
• The regional investigator meetings/presentation of materials; the development of regional enrolment initiatives; and planning regional clinical study supplies.
• To assist in obtaining the required translations, collecting non-essential documents from site and ensuring sites are trained in collaboration with the site monitor.
• To support database lock activities

 

Requirement

• Degree in Science or health-related field

• Previous working experience in clinical study

 

Interested candidates please send in your resume to:

 

[Click Here to Email Your Resume]

 

EA Personnel: Valerie Yong Kian Fung
CEI No.: R1103704

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