Your Exciting Role
- Responsible for project management throughout project phases including initiation, design, execution, and completion, ensuring compliance with regulatory requirements and Good Clinical Practice (GCP).
- Creating SOP, WI, WO, FORM, and others related to the document management system, especially in the scope of R&D project management.
- Responsible for controlling and monitoring project objectives, including clinical trial timelines, site performance, and regulatory compliance.
- Co-manage the reimbursable invoices reconciliation process.
- Responsible for exploring creative solutions for common project budget and timeline problems to ensure effective and transparent monitoring while mitigating risks in clinical research.
- Identify and resolve any issues related to protocol deviations, adverse events, or compliance risks at the site.
- Develop relationships with clients and vendors, identifying moments to leverage emerging opportunities.
- Prepare weekly and monthly performance reports for timeline and budgeting of R&D projects.
Ideally, You Would Have
- Passionate in preserving Indonesia biodiversity through sustainable innovations.
- Bachelor of Science in Biology, Pharmaceuticals, Chemistry, Chemical/Industrial Engineering or other related major.
- Has experience in Project Management, Clinical Research, Laboratory and the molecular biology techniques are an added value.
- Good computer skills, experience with Microsoft Office also laboratory system.
- Having a good communication and interpersonal skills.
- Thorough & nimble, finished report within time scheduled.
- Able to work with team.