Clinical Trial Assistant

Role & responsibilities :

• Prepare and send EC and SIV dossier to site as per instructions from COM/CPM/CRA and
  instructions outline in SOPs.
• Dispatch clinical trial supplies to respective sites for ongoing studies as per the requirement.
• Coordinate with study sites for ongoing studies as per the need.
• Assist CRAs to update in-house files and perform quality review of in-house files as define in
  the study plans and convey the outcome to the CRAs.
• Maintain and update the study trackers (for.e.g. Study documents, Finance, Study equipment
  etc.) as per define frequency.
• Review invoices received from respective sites in a timely manner and convey the outcome
  to respective CRA and site team as applicable.
• Provide in-house support to CRAs for ongoing studies
• Prepare minutes of meetings for Important study related discussion as instructed by
  COM/CPM.
• Assist training coordinator to coordinate departmental training as per the training calendar.
• Complete other assigned activities per the need of the study and Organization.

Preferred candidate profile :

• Thorough understanding of ICH-GCP
• Good communication skills
• Ability to work under pressure
• Multi-tasking ability
• Ability to work independently Eye for detail
• 2-3 years of experience in Pharma/Biotech/CROs in Clinical Research would be preferred.

Perks and benefits