Medical Affairs Officer

PSI is a leading Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.

At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.

We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.

At PSI, Medical Affairs Officer provides support to various positions in Medical Affairs department, builds and maintains sites relationships, participates in feasibility research and enrollment boosting endeavors.

We are looking for a highly organized and proactive professional to join our team in Sofia, Bulgaria in a hybrid role supporting both administrative operations and feasibility assessments in clinical trials. This role offers a unique opportunity to contribute to the efficiency of our clinical research processes while also playing a key role in site and investigator feasibility evaluations.

Your role:

• Support Medical Monitors, Medical Data Reviewers or Pharmacovigilance Physicians depending on assignment to global trial programs.
• Liaise with Medical Affairs sub-functions to boost the resolution of assigned safety or quality tasks.
• Conduct onsite visits to clinical trial sites to support patient recruitment and retention.
• Build and maintain relationship with investigators, gather investigator feedback and insights to optimize project performance and site experience.
• Consolidate actionable medical insights and provides relevant information to department management.
• Conduct site and investigator feasibility assessment to identify suitable clinical trial locations.
• Assist in preparing feasibility questionaries.
• Take part in enrollment boosting initiatives to optimize site performance.
• Build and maintain strong relationships with clinical trials sites to ensure successful collaboration.

• Medical Doctor degree, board certification in a major therapeutic area is a plus
• Minimum 2 years of experience as a practicing physician (including internship/residency)
• Prior experience in clinical research
• Full working proficiency in English and Bulgarian
• Proficiency with MS Office applications
• Communication, presentation and analytical skills
• Problem-solving, team and detail-oriented

Join our highly dedicated team of clinical research professionals with +250 Medical Doctors onboard, and make a tangible difference within a professional and energetic organization founded by scientists.