A. Primary function
• Perform high quality research activities.
• Provide technical support to the pharmaceutical research and training teams.
• Responsible for maintenance and preparation of the pharmaceutical research equipment.
• Participate in innovative research and development programs.
• Maximize the academic research profile of the company by actively participating and organizing international conferences and workshops.
• In collaboration with the pharmaceutical development manager, contribute to the development and implementation of the pharmaceutical plan of R&D projects under his/her responsibilities.
• Design the clinical development plan of all R&D projects of the group in accordance with current regulatory guidelines.
• Monitor, create and manage of intellectual property.
• Coordinate project activities to ensure that new projects are delivered on time
• Project planning and communication of project status on a regular basis
• Meeting and Reports
1. Participate to monthly R&D meeting.
2. Provide weekly update on the status of the projects/ clinical studies.
• Manage the budget of R&D projects under his/her responsibilities
1. For projects under his/her responsibilities, identify resources requirements and elaborate a budget plan including the pharmaceutical development budget (in collaboration with the pharmaceutical manager).
2. Elaborate clinical development plan budget including timelines and milestones.
3. Respect allocated budget.
• Organize, schedule and coordinate workloads for team members.
• Enforce safety procedures and reports safety incidences.
B. Perform other related duties that may be assigned from time to time.
Job qualifications
- A BS in Chemistry, Chemical Engineering, or a similar field is required
- Must be a Licensed Chemist or Chemical Engineer
- At least five (5) years of experience in a pharmaceutical company, with at least two (2) years in a supervisory role
- Comprehensive understanding of Good Clinical Practices and International Clinical Regulatory Requirements
- Strong knowledge of the drug development process
- Excellent problem-solving ability
- Ability to multitask
- Good moral character.
- Willing to be assigned in Bancal, Carmona, Cavite
Summary of role requirements:
- Looking for candidates available to work:
- Monday: Morning, Afternoon
- Tuesday: Morning, Afternoon
- Wednesday: Morning, Afternoon
- Thursday: Morning, Afternoon
- Friday: Morning, Afternoon
- 2-3 years of relevant work experience required for this role
- Working rights required for this role
- Expected start date for role: 26 October 2024