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Building Biotechs - Clinical Development & Medical Affairs
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:
* 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.
Seniority level
* Mid-Senior level
Employment type
* Contract
Job function
* Research
* Industries
* Medical Practices
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