Clinical Trial Manager

Summary

Join our growing team as an experienced Clinical Trial Manager! This remote position, available across several European countries, offers the chance to lead and manage clinical trials across multiple countries. You will be responsible for all clinical aspects of your studies, ensuring timely and high-quality delivery. We seek highly organized, detail-oriented professionals with strong communication skills and a proactive approach to risk management. The role involves collaboration with various teams and clients, mentoring team members, and ensuring client satisfaction. If you thrive in dynamic environments and enjoy a consultative approach to trial management, this is the perfect opportunity for you.

Requirements

• Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in the field of oncology
• Demonstrable experience leading clinical aspects of your studies across multiple countries in a CRO / Pharma or Biotech company (in a dedicated 'clinical lead' role)
• Working knowledge of GCP/ICH guidelines and the clinical development process
• Availability for domestic and international travel including overnight stays
• Must be able to communicate effectively in the English language
• Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)
• Demonstrated ability to develop positive working relationships with internal and external organizations
• Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan
• Demonstrates mastery knowledge of ICH-GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement

Responsibilities

• Management and operational delivery of the clinical elements within a trial including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out
• Successful execution of assigned trials and ensuring completion of trial deliverables
• Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by working in close collaboration with other functional team members
• Mentoring and training of team members
• Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor
• Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities
• Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve the highest level of client satisfaction

Preferred Qualifications

• You love having responsibility and a say in how clinical trials are run
• You plan ahead, but have alternative options and a flexible approach
• You are client focused
• You are well organised and able to manage timelines and shifting priorities, without sacrificing quality
• You communicate clearly, often and concisely and know that your role is crucial in keeping the trial running smoothly
• You are a master at identifying any risks that threaten projects and handle them resolutely
• You thrive and work with autonomy and ownership to deliver successful outcomes

Benefits

Remote work