Freelance Clinical Trial Manager

EPM Scientific; Deutschland; Remote; EUR 70.000 - 100.000; Vollzeit

Zusammenfassung

A growing CRO seeks a Freelance Clinical Trial Manager to oversee clinical operations across various trials in Oncology and Infectious Diseases. The ideal candidate will have over 5 years of experience in Clinical Operations, strong organizational skills, and a comprehensive understanding of regulatory compliance. This remote role allows for flexible start dates and offers the opportunity to lead and manage clinical trials on a global scale.

Qualifikationen

• 5+ years experience in Clinical Operations.
• In-depth knowledge of GCP and regulatory requirements.
• Proven leadership and team management abilities.

Aufgaben

• Lead the planning, execution, and management of multiple clinical trials.
• Ensure compliance with regulatory requirements and GCP guidelines.
• Manage trial budgets and timelines, ensuring efficient resource use.

Kenntnisse

Clinical Operations

Leadership

Time Management

Communication

Jobbeschreibung

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.