Clinical Trial Manager
EPM Scientific are currently working with a Mid-sized Pharmaceutical Company, who are seeking a Clinical Trial Manager to join their team for a Hematology study in Switzerland. See a short summary below:
Contract Conditions:
- Start date: June, Flexible
- Location: Schwyz, Switzerland
- Contract Type: Permanent, Full time
- Language: English and German
- Project: Clinical Trial Management, Hematology Study
Key Responsibilities:
- Oversee the planning, execution, and management of clinical trials in hematology.
- Ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.
- Coordinate with cross-functional teams, including data management, biostatistics, and regulatory affairs.
- Develop and maintain trial documentation, including protocols, case report forms, and informed consent forms.
- Monitor trial progress, including patient recruitment, data collection, and site management.
- Manage 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.
Requirements:
- Experience in Clinical Operations required, previous CTM experience not required, CRAs considered
- 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.
- 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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