Global Study Manager - Single Sponsor Dedicated (In Emea)

Job Description

Review relevant client SOPs and guidelines (e.g., description of services and transfer of obligations).

Take on assignments on non-drug project work in process improvements and/or lead improvement projects as discussed and agreed upon with their manager.

Qualifications

University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research.

Relevant experience from within the pharmaceutical industry or similar organization or academic experience, preferably of at least 3 years.

Knowledge of clinical development / drug development process in various phases of development and therapy areas.

Excellent knowledge of international guidelines ICH/GCP.

Excellent communication and relationship building skills, including external service provider management skills.

Good project management skills.

Demonstrated ability to collaborate as well as work independently.

Demonstrated leadership skills.

Computer proficiency, advanced computer skills in day-to-day tasks.

Excellent verbal and written communication in English.

Salary & Benefits
The potential base pay range for this role, when annualized, is  zł -  zł. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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