Clinical Trial Manager - Remote

1w1 week ago

Precision for Medicine

RS · Full-time · €75,000 – €110,000

About this role

Precision for Medicine, a precision medicine CRO, seeks an experienced Clinical Trial Manager for its growing team. Candidates can work remotely in UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia. You will serve as the hub of central intelligence, leading CRAs and overseeing all clinical aspects across multiple countries to ensure timeline adherence, scope, and quality delivery.

The role involves management and operational delivery of clinical elements, including site selection, start-up, enrolment management, site engagement, monitoring planning, data cleaning, and close-out. You will ensure successful execution of assigned trials, completing deliverables while collaborating closely with functional team members on communication, regulatory documentation, and oversight.

Thrive in a dynamic environment addressing challenges in oncology R&D, with a consultative approach to trial management. Lead CRAs in establishing site relationships for high-quality oversight of monitoring, regulatory, IP, site payments, and correspondence. Maintain team focus on priorities through efficient cross-functional partnerships for top client satisfaction.

Mentor and train team members while identifying challenges to timelines and offering creative action plans. Work with autonomy and ownership on studies impacting patient health worldwide. Join high-energy professionals passionate about rare diseases, oncology, and precision medicine.

Requirements

Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in oncology
Demonstrable experience leading clinical aspects of studies across multiple countries in a CRO, Pharma or Biotech company in a dedicated 'clinical lead' role
Significant clinical trial management experience in oncology
Working knowledge of GCP/ICH guidelines and the clinical development process
Availability for domestic and international travel including overnight stays
Ability to communicate effectively in English
Client focused with well organised approach to manage timelines and shifting priorities without sacrificing quality
Skilled at identifying risks that threaten projects and handling them resolutely

Responsibilities

Manage and operationally deliver clinical elements of trials including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out
Ensure successful execution of assigned trials and completion of trial deliverables
Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by collaborating with functional team members
Mentor and train team members
Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor
Lead CRAs to establish relationships with sites for high quality oversight of monitoring, regulatory, IP, site payment and site correspondence activities
Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve highest level of client satisfaction

Benefits

Remote work available in UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia
Autonomy and ownership in delivering successful trial outcomes
Opportunity to impact health and lives of patients through oncology and rare disease trials