Deskripsi Pekerjaan
Are you looking for a challenging role at the intersection of science and healthcare? Allied Search Pte. Ltd. is currently seeking a highly motivated Medical Affairs Associate to join our team in the Central Region. This is a fantastic opportunity to leverage your background in the pharmaceutical sector to drive medical strategy and ensure compliance across the organization.
As a Medical Affairs Associate, you will play a key role in supporting the execution of medical plans, managing regulatory interactions, and providing scientific support to internal stakeholders. You will work closely with cross-functional teams to ensure that medical information is accurate and aligned with regulatory standards. We value candidates who are proactive, detail-oriented, and possess a deep understanding of the regulatory landscape. If you are ready to take the next step in your career with a dynamic company, we want to hear from you.
Tanggung Jawab
- Support the execution of Medical Affairs strategies, including medical information, scientific communications, and clinical development projects.
- Assist in the preparation, compilation, and submission of regulatory dossiers and clinical trial applications (CTAs).
- Monitor medical literature and competitor activities to provide insights on market trends and scientific developments.
- Ensure strict adherence to Good Medical Practice (GMP) and internal Standard Operating Procedures (SOPs) across all activities.
- Coordinate with cross-functional teams (Clinical, Regulatory, Marketing) to align on medical objectives and deliverables.
- Manage incoming medical inquiries from healthcare professionals and internal stakeholders with a focus on accuracy and timeliness.
- Contribute to the maintenance and update of medical databases and regulatory filing systems.
Kualifikasi
- Bachelor’s degree in Life Sciences, Pharmacy, Medicine, Nursing, or a related field.
- Relevant experience in Medical Affairs, Regulatory Affairs, or Clinical Research within the pharmaceutical or biotechnology industry.
- Strong understanding of pharmaceutical regulations, compliance requirements, and the clinical development process.
- Excellent written and verbal communication skills, with the ability to translate complex scientific data into clear messages.
- Proficiency in MS Office Suite (Word, Excel, PowerPoint) and familiarity with medical software (e.g., Veeva Vault, Medidata Rave).
- High level of attention to detail and the ability to manage multiple priorities in a fast-paced environment.
- Proactive problem-solving skills and a commitment to ethical standards in medical practice.