Clinical Trial Manager - Remote

1w1 week ago

Precision for Medicine

HU · Full-time · €65,000 – €95,000

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. The role focuses on novel clinical trial designs, operational expertise, biomarker analytics, and passion for rare diseases and oncology.

You will serve as the hub of central intelligence for studies, leading CRAs and overseeing all clinical aspects across multiple countries. Ensure timeline adherence, scope management, and quality delivery in dynamic environments. Thrive as a high-energy professional who enjoys challenges and details.

Take a consultative approach to trial management, proving a valuable partner in operational delivery. Address challenges in oncology R&D to impact patient health worldwide. Client-focused traits like clear communication and risk handling keep trials running smoothly.

Day-to-day involves site selection, monitoring execution, data cleaning, and close-out, with mentoring of team members. Identify timeline risks and offer creative action plans. Foster cross-functional partnerships for client satisfaction and successful outcomes.

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
Well organised with ability to manage timelines and shifting priorities without sacrificing quality
Master at identifying risks that threaten projects and handling them resolutely

Responsibilities

Manage and operationally deliver clinical elements including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out
Execute assigned trials ensuring 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 site relationships 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 for highest client satisfaction

Benefits

Remote work available in UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia
Opportunity to work on precision medicine trials in oncology and rare diseases
Support for continued growth through mentoring and training team members