Clinical Operations Director
EPM Scientific are currently working with a Biotech with an exciting pipline, who are seeking a Clinical Operations Director to join their team in Switzerland. See a short summary below:
Contract Conditions:
- Start date: May/June, Flexible
- Location: Switzerland
- Contract Type: Permanent, Full time
- Language: English and German
- Project: Wound Care
Responsibilities
- Lead the planning, execution, and management of clinical operations across multiple trials.
- Ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.
- Coordinate with cross-functional teams, including data management, biostatistics, regulatory affairs, and clinical trial managers.
- Develop and maintain comprehensive trial documentation, including protocols, case report forms, and informed consent forms.
- Oversee trial progress, including patient recruitment, data collection, and site management.
- Manage and optimize trial budgets and timelines, ensuring efficient use of resources.
- Serve as the primary point of contact for investigators, sponsors, and regulatory authorities.
- Conduct site visits and audits to ensure adherence to study protocols and regulatory requirements.
- Provide strategic direction and leadership to the clinical operations team.
Requirements:
- Extensive experience in Clinical Operations, with a strong background in managing clinical trials.
- In-depth knowledge of GCP and regulatory requirements.
- Excellent organizational and time management skills.
- Ability to work independently and manage multiple priorities in a fast-paced environment.
- Strong communication and interpersonal skills.
- Proven leadership and team management abilities.
- Willingness to travel occasionally.
If this role is of interest to you, please apply directly to learn more. If not, feel free to share with your network.
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