Who We Are Celebrating 40+ years! Theradex Oncology is a full-service CRO specializing in oncology. The company manages global oncology trials and programs. The company was founded in 1982 working with the National Cancer Institute, which led to its expansion to working with industry sponsors developing cancer therapeutics. As a service-based company we support both domestic and international sponsors in the conduct of both early and late phase trials. What You'll Do As part of Theradex Oncology, you will have the opportunity to work with one of the largest professional teams focused solely on the development of cancer therapies. Cancer research continues to evolve as new therapies and therapeutic approaches are discovered, as part of the team you will work to support our sponsors in the development of these therapies. Theradex Oncology is an environment for highly motivated individuals who want to make a difference. We are hiring a Full time Permanent CRA (Trainee) in United Kingdom (Home Based). The CRA trainee program offers talented applicants an entrance ticket to many career pathways within the pharmaceutical industry. Theradex Oncology is a full-service Contract Research Organization (CRO). Theradex assist the pharmaceutical industry with the complete set of services that is required to bring a product from first-in-man to market registration. Talented candidates are able to reach the Senior CRA position from the CRA trainee program. Other career pathways may subsequently be available within the full service offering to our clients. We encourage applications by multilanguage applicants. This role requires fluency English language, plus a second European language is advantageous. The primary responsibilities of this position include, but are not limited to, the following:
Complete all company specific trainings timely once assigned.
Successful completion of provided CRA Trainee course within 6 months of employment start.
Act as administrative support to PMs, CRAs and functional area leads during CRA Trainee period.
Assist in the day to day running of projects assigned.
Assist in the preparation of project specific materials e.g., status reports, newsletters, templates, etc.
Participate in project administration as required e.g., photocopying, binder preparation, start-up pack preparation etc.
Maintain an awareness of the literature on cancer therapy, clinical trial design and conduct, and good clinical practice.
Work in collaboration with on-site CRAs to meet Sponsor, Protocol and Theradex objectives of Regulatory Readiness including contract and budget negotiations, as required.
Assist on routine communications with study sites, providing study updates and support to sites and providing project team updates on site related issues.Ensure site communications are documented and archived as per project requirements and Theradex Oncology SOPs.
Responsible for assisting in the preparation of the Investigator and Sponsor files with essential documents for the initiation of sites participating in clinical studies.
Assist study staff with maintaining the sponsor files during the life of the study.
Assist in archiving at the end of study in accordance with relevant SOPs, policies and local regulatory.
Posting details
Remote
Yes
Employment type
Full-time
Workplace type
Remote
Source
remotejobsorg
First seen
9/20/2026, 8:10:25 AM
Last seen
9/20/2026, 8:10:25 AM
Maintain/up-date site information (including all contact details, contracts, and reports).
Performs ongoing management of essential regulatory documentation at the outset and across the lifespan of a study, such as:
Essential document collection, review, upload, maintenance, and close-out activities, ensuring that that sponsor and investigator obligations are being met and follow applicable local regulatory requirements and ICH/GCP guidelines.
Perform Site Essential Documentation verification prior to upload into the eTMF.
Performs quarterly QC of each study in the eTMF according to Theradex Oncology SOP.
Performs study tracking via CTMS, investigator site file tracker (if utilized) and/or sponsor designated system to ensure that the study files are current, accurate and complete.
Ensures protection of subjects, subjects' rights, and the integrity of data through adherence to Good Clinical Practice, applicable regulatory requirements, Standard Operating Procedures, and protocol compliance.
Assist in the conduct of pre-qualification, initiation, routine monitoring, remote monitoring, and close-out visits in accordance with the relevant SOPs to include but not limited to:
Source document review and comparison to CRF data
CRF review/retrieval and data corrections
IMP accountability
Maintenance of on-site investigator files
IEC/IRB documentation
Local laboratory documentation
Maintenance of investigational supplies
Subject consent and consent process review (Informed Consent Form and source documentation)
Verify patient eligibility
Assess protocol compliance and deviations
Handling of safety and efficacy issues, including, but not limited to:
Serious adverse event reports
Adverse event trends
Treatment failures
Assist with site visit report preparation within study specific timeframe
Assist with all aspects of site management as described in the study plans
Proactively identify and resolve potential site and study issues.
Identify and escalate data quality issues to ensure clinical data integrity
Provide support to project management via ongoing project reports and updates.
May be responsible for supporting multiple studies simultaneously
Must prioritize appropriately to meet business needs to ensure on-time, quality deliverables.
Perform other duties as assigned by management. What You Need Level of Education & Prior Experience
PhD in a life science field or equivalent.
Oncology knowledge is required
Previous experience with Clinical Research Site Coordination or related fields (i.e. Regulatory Specialist) preferred.
Previous experience in monitoring (i.e. In-House CRA/CTA/CMA) or equivalent experience) preferred.
Study Start up experience is an advantage Skills and Competencies
Professional attitude with good customer focus.
Strong communication skills: verbal/written/presentation.
Good interpersonal skills, including persuasion and influence.
Able to work independently as well as in a group.
Good time management, multitasking and execution skills.
Good organizational skills, including efficiency, punctuality, and collaboration in a team environment.
Demonstrated proficiency in Microsoft Outlook, Word, and Excel.
Technically proficient enough to work in a remote environment and able to address minor technical challenges without support but will timely escalate to Information
Technology Support for challenges beyond capabilities.
Capable of absorbing and applying knowledge gained through internal and external trainings on protocols assigned.
Knowledge of ICH Guidelines and GCP including an understanding of regulatory requirements.
Effective knowledge of the drug development process and the Theradex organizational structure Additional Requirements
This position involves international and/or national travel as needed to meet study requirements. Ability to travel domestically and/or internationally and may involve overnight stays. Travel requirements are up to 70%.
Valid Driver’s License preferable.
Passport essential
Successfully pass background clearance checks which may be run on a periodic basis due to 3rd party contractual obligation requirements.
Fluent in English and preferably at least one other European language if applicable What we offer: We offer a friendly and supportive culture that puts people first. We provide a competitive compensation and benefits package including 6% pension contribution, private medical insurance, sick pay and income protection insurance, life assurance and eyecare voucher scheme. This job does not offer company sponsorship Theradex is an equal opportunity employer. All qualified applicants are encouraged to apply and will receive consideration for employment.