EPM Scientific are currently working with a small & growing CRO, who are seeking a Freelance Clinical Trial Manager to join their team. See a short summary below:
Contract Conditions:
* Start date: May/June, Flexible
* Location: Europe, Remote
* Contract Type: Freelance / Consultant
* Language: English essential, additonal Languages are a plus
* Project: CRO Oncology, Hematology, Infectious Disease
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:
* Strong (5+ years) experience in Clinical Operations, with a strong background in managing global 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.