Global Study Manager

This is a fully remote position, open to applicants in Poland, +1 more country.

📋 Description

• Oversee the daily operations of clinical trial management activities.

• Plan and coordinate all elements of clinical trials, ensuring compliance with timelines, budgets, and quality benchmarks.

• Work collaboratively with cross-functional teams to establish and execute clinical trial protocols and procedures.

• Cultivate and maintain relationships with trial investigators and stakeholders.

• Ensure that trials adhere to local, national, and international regulations as well as ethical standards.

• Tackle problems and make essential decisions regarding trial design, vendor selection, and risk management.

• Assist the team and stakeholders in achieving high-quality outcomes across clinical programs.

• Guide the team and manage competing priorities effectively.

⛳️ Requirements

• A university degree in medicine, science, or a relevant combination of education and experience.

• Strong experience in clinical trial management.

• Proven track record of driving the clinical deliverables of a study.

• Expertise in the specified therapeutic area.

• Previous monitoring experience is preferred.

• Willingness to travel as necessary (approximately 25%).

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellbeing programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellbeing resources.

• Opportunities for learning and development through structured training and career pathways.