We are looking for a Senior CRA with a strong knowledge of multiple myeloma and a passion for oncology to work with our client on UK based studies. Ideally London or Manchester based as there are significant sites and patients in those places but we are open to UK wide candidates with good multiple myeloma heam-oncology backgrounds. The background with research in multiple myeloma would be a huge bonus as you would need to train the teams and sites in the nuance of repsonsiveness and outcomes in this disease. 

Job Summary: We are seeking a Clinical Research Associate with expertise in conducting early Phase Oncology clinical trials in oncology and ideally multiple myeloma. The CRA will be responsible for managing and monitoring clinical studies in compliance with Uk regulations, Good Clinical Practice (GCP) guidelines, and study protocols. 

This role will involve ensuring adherence to local clinical trials regulations specific to early Phase I studies, coordinating with local regulatory authorities and ethics committees, and providing guidance on local requirements for early Phase oncology trials.

Responsibilities:

Manage and oversee the conduct of early Phase clinical trials in the UK with centres in London and Manchester, ensuring compliance with local regulations, GCP, and study protocols

Ensure timely submission of trial-related documents specific to early Phase trials to the appropriate regulatory authorities and ethics committees, following the requirements outlined in the legislation.

Coordinate with local regulatory authorities, for obtaining necessary approvals, authorizations, and amendments related to the studies.

Liaise with local ethics committees to obtain ethical approvals for the initiation and continuation of the studies.

Provide guidance and expertise on specific requirements for  trial conduct, including informed consent processes, data protection regulations, and reporting obligations specific to these studies.

Conduct site selection visits and assess potential investigational sites for participation in the studies, considering local feasibility and regulatory requirements.

Initiate, monitor, and close out early phase oncology studies clinical trial activities at investigative sites in compliance with study protocols, GCP, and local regulations.

Train site staff on regulatory requirements specific to the studies, GCP guidelines, and study-specific procedures.

Ensure proper documentation and maintenance of trial-related files specific to early phase oncology studies, including essential documents and trial master files, in accordance with local regulations regulations and company SOPs.

Perform routine monitoring visits to assess data integrity, protocol compliance, and patient safety, while also ensuring compliance with local regulations specific to early phase oncology studies.

Collaborate with cross-functional teams, including data management, project management, and medical affairs, to ensure the successful execution of early phase oncology studies

Keep up-to-date with changes in local regulations clinical trials regulations specific to early phase oncology studies and disseminate knowledge to study teams and relevant stakeholders.

Qualifications:

Bachelor's degree in a scientific or healthcare-related field (Master's degree preferred).

Strong experience as a Clinical Research Associate/ Senior CRA, with specific experience in conducting oncology clinical trials in UK

In-depth knowledge of local regulations clinical trials regulations

Strong understanding of GCP guidelines and their application in  oncology studies.

Experience in managing submissions to local regulations regulatory authorities and ethics committees for early phase oncology studies.

Excellent knowledge of local regulations-specific requirements for informed consent, data protection, and adverse event reporting specific to early phase oncology studies.

Familiarity with the local regulations healthcare system and regulatory landscape related to early phase oncology studies.

Excellent communication and interpersonal skills, with the ability to build and maintain relationships with investigators, site staff, and cross-functional teams.

Detail-oriented with strong organizational and time management skills.

Proficiency in using electronic data capture (EDC) systems and other clinical trial management

Please contact Henry Grover or Gail Kniveton for more information 

02089850565

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