Site SSU Lead – Poland

This is a fully remote position, open to applicants in Poland.

📋 Description

• Leading and guiding site activation teams across worldwide clinical programs.

• Collaborating with Clinical Operations teams to enhance study start-up performance and timelines.

• Utilizing data, forecasting tools, and industry insights to assist in planning and decision-making.

• Crafting country-specific Informed Consent Forms (ICFs) in accordance with local regulations and approved templates.

• Identifying avenues to optimize processes and foster continuous improvement.

• Tracking study progress, proactively managing potential delays, and escalating issues as necessary.

• Offering mentorship and support to members of the study start-up team.

• Partnering with internal stakeholders to ensure sites achieve "Ready to Enroll" status as effectively as possible.

• Serving as a primary point of contact for study start-up challenges and assisting teams in finding efficient solutions.

⛳️ Requirements

• Bachelor's degree in Life Sciences or a related field (or equivalent experience).

• Over 4 years of experience in clinical operations, study start-up, project management, or trial optimization.

• A minimum of 2 years of hands-on experience managing site activation and study start-up activities within a CRO or pharmaceutical setting.

• Experience in developing country-level Informed Consent Forms (ICFs).

• Strong analytical capabilities with experience in using data, forecasting tools, and performance metrics.

• Ability to interpret complex information and convey it clearly to diverse audiences.

• Solid comprehension of the factors that contribute to effective study start-up and site activation.

• Previous experience in a global clinical research environment is highly preferred.

• Excellent communication, organizational, and stakeholder management skills.

🏝️ Benefits

• Be part of a global team dedicated to enhancing patient outcomes through clinical research.

• Work in a collaborative and supportive atmosphere where your ideas are appreciated.

• Influence the success of international clinical trials and assist in delivering new treatments to patients more swiftly.

• Take charge of significant projects and contribute to process enhancements on a global scale.

• Enjoy opportunities for professional growth and career advancement within a leading CRO.