At a Glance
- Tasks: Oversee clinical trials in haemato-oncology, ensuring compliance and data quality.
- Company: Join a not-for-profit dedicated to improving blood cancer outcomes through clinical trials.
- Benefits: Remote work, competitive salary, and the chance to make a real impact on patient care.
- Other info: Work independently in a dynamic environment with opportunities for professional growth.
- Why this job: Be part of a mission-driven team that accelerates access to life-saving treatments.
- Qualifications: Experience in clinical trials and strong communication skills are essential.
The predicted salary is between 37800 - 46200 £ per year.
Company Description Accelerating Clinical Trials Ltd (ACT) is a not-for-profit organization focused on improving outcomes for people with blood cancer by accelerating access to clinical trials.
Any surplus income is reinvested to directly benefit blood cancer patients, reflecting a strong commitment to patient-centered care and impact.
ACT provides resources and specialist expertise to speed up delivery of both academic, investigator-initiated studies and industry-sponsored clinical trials in haemato-oncology.
Through close collaboration with established networks such as TAP and IMPACT, ACT supports efficient trial setup, recruitment, and management across multiple sites.
Role Description The Senior Clinical Research Associate (CRA) is a full-time, remote role responsible for overseeing the conduct of haemato-oncology clinical trials from start-up through close-out.
Day-to-day activities include monitoring trial sites, ensuring adherence to study protocols, verifying source data, and maintaining high standards of data quality and regulatory compliance.
The role involves collaborating with investigators, site staff, sponsors, and internal clinical operations teams to resolve issues, manage timelines, and support patient safety.
The Senior CRA will contribute to protocol review, training of site personnel, and continuous process improvement to ensure efficient trial delivery within ACT’s academic and industry portfolios.
Qualifications Clinical trial expertise, including strong knowledge of Clinical Trials processes and experience working as or with Clinical Research Associates.
Proficiency in interpreting and applying study Protocol requirements in operational settings.
Experience in Clinical Operations, including site monitoring, trial management, and coordination with cross-functional teams.
Solid background in Research methods and good clinical practice (GCP), particularly in haemato-oncology or oncology.
Bachelor’s degree or higher in life sciences, nursing, pharmacy, or a related discipline.
Demonstrated ability to work independently in a remote setting, manage multiple studies, and meet deadlines.
Strong written and verbal communication skills, with attention to detail and documentation accuracy.
Experience with electronic data capture systems and common clinical trial management tools; familiarity with regulatory requirements and ethics submissions.
Senior Clinical Research Associate in Lincolnshire employer: Accelerating Clinical Trials Ltd
Accelerating Clinical Trials Ltd (ACT) is an exceptional employer dedicated to making a meaningful impact in the lives of blood cancer patients. With a strong focus on patient-centered care, ACT fosters a collaborative and supportive work culture that encourages professional growth and development. Employees benefit from the flexibility of remote work while being part of a mission-driven organisation that reinvests its resources to enhance clinical trial access and outcomes.
Contact Details:
Accelerating Clinical Trials Ltd Recruitment Team
