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.