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

📋 Description

• Oversee all tasks related to the initiation and monitoring of a study

• Prepare precise study status reports and manage study documentation

• Efficiently handle sponsor-generated queries

• Ensure cost efficiency of the study

• Engage in the preparation and assessment of study documentation and feasibility analyses for new proposals

• Build and sustain collaborative relationships with key stakeholders, clinical investigators, and site personnel

• Safeguard patient safety and adherence to ICON's protocols, procedures, and regulatory standards

⛳️ Requirements

• Bachelor's degree in medicine, science, or a related field

• Familiarity with ICH-GCP guidelines

• Ability to review and assess medical data

• Strong written and verbal communication skills in both English and German

• Laboratory experience and/or capability to analyze laboratory results

• Strong interpersonal skills to address queries promptly

• Willingness to travel as necessary (approximately 60%)

• Legal eligibility to work in the country where the position is located

🏝️ Benefits

• Competitive base salary along with performance-related incentives

• Health and wellness programs, which may include medical, dental, and vision coverage

• Retirement and pension schemes

• Life insurance and disability coverage

• Employee assistance programs and wellness resources

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