Director, Clinical Trial Management
vor 1 Tag
Proclinical are searching for a highly experienced and innovative Director of Clinical Trial Management to join our client, a clinical-stage biotech organisation specialised in radio-immune therapies.
Report into: Head of Clinical Operations
**Responsibilities**:
- Develop and implement clinical trial processes and procedures to ensure compliance with applicable regulatory regulations.
- Prepare and review essential study documents such as protocols, informed consent forms, and standard operating procedures.
- Manage and coordinate the operational aspects of clinical trials, including recruitment, monitoring, data collection, and management.
- Assist with the development of clinical trial budgets and timelines.
- Conduct site evaluations and selection at potential investigative sites.
- Track and monitor clinical trial performance and progress.
- Execute clinical trial reporting and data management.
- Monitor patient safety and data quality.
- Provide support for the preparation of regulatory submissions.
- Ensure compliance with applicable regulations and good clinical practice guidelines.
**Requirements**:
- Bachelor's degree in life sciences, medicine, or a related field.
- At least 6 years of experience in clinical trial management.
- Excellent written and verbal communication skills.
- Strong organisational and analytical skills.
- Ability to handle multiple tasks and meet deadlines.
- Proficiency in MS Office and project management software.
- Knowledge of applicable regulations and standards in clinical research.
- Team player with a passion for innovation and problem solving.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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