Overview
We are currently hiring for an international specialty pharmaceutical organisation advancing innovative treatments. We are looking for a Medical Manager to provide scientific and medical leadership across clinical programs, ensuring high-quality study design, execution and oversight.
Responsibilities
- Lead medical oversight for clinical studies, including protocol development and Quality-by-Design principles.
- Act as medical monitor: safety review, medical queries, oversight of study conduct.
- Support development of CRFs, Medical Monitoring Plans, and Clinical Study Reports.
- Maintain strong relationships with investigators and clinical sites.
- Provide medical input to pharmacovigilance activities for clinical and post-authorisation studies.
- Review clinical and safety data; identify risks and propose solutions.
- Ensure inspection readiness and support GCP audits/inspections.
- Contribute to process improvements, digital trial initiatives, and cross-functional knowledge transfer.
- Provide internal scientific training and represent the organisation at scientific meetings.
- Support communication with regulatory authorities as required.
Qualifications
- MD (or equivalent)
- 4+ years experience in clinical research/clinical development.
- Strong knowledge of ICH/GCP and global clinical trial regulations.
- Experience in medical monitoring, protocol development, and clinical data review.
- Excellent written and verbal communication skills.
- Strong analytical, decision-making, and project leadership abilities.
- Ability to work independently, manage deadlines, and solve problems quickly.
Benefits
- Competitive salary and benefits.
- Opportunity to impact patient care and contribute to meaningful scientific progress.
- High exposure to senior scientific experts and strategic programs.
- Collaborative, intellectually driven environment focused on clinical excellence.
- Hybrid work model with three days on-site.
