Senior Clinical Research Associate (UK)
Company: Theradex Oncology
- Location: United Kingdom
- Seniority: Senior
- Employment type: Full-time
- Posted: 13 days ago
- Offer language: English
Job description
We are hiring a Full time Freelance SCRA/CRA-II in the UK, preferably London area on a 6 month contract (Inside IR35)
The Sr. Clinical Research Associate (Sr. CRA) will be responsible for performing investigative site management and monitoring activities throughout the clinical trial lifecycle on behalf of multiple sponsors. To drive our success, we are seeking an experienced onsite monitor who can join our team of highly skilled CRAs committed to delivering high quality results on behalf of our valued client
Level of Education:
- At minimum, Bachelor's degree (BSc, BA, or RN equivalent) in biological or human science-related field or equivalent experience.
Prior Experience:
- At least 5 years’ experience as a Clinical Research Associate with a sound track record in managing clinical trial sites
- Experience in on-site monitoring oncology early phase studies
- CRO/Pharmaceutical industry experience
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% in the UK
- Valid Driver’s License and Passport preferable.
- Successfully pass background clearance checks.
- Must be confident in applying RECIST criteria in oncology trials. 3 years experience of using RECIST in more than one study.
- Candidates should have experience in monitoring Phase I–III oncology studies? at least 3 years of oncology experience in more than one oncology study.
Skills and Competencies to be demonstrated:
- Thorough knowledge of ICH Guidelines and GCP including an understanding of regulatory requirements.
- Highly effective multitasking and execution skills.
- Excellent interpersonal skills, including communication, presentation, persuasion, and influence.
- Excellent organizational skills, including efficiency, punctuality, and collaboration in a team environment.
- Knowledgeable in the identification, anticipation, and reporting to appropriate management problems relating to study conduct, and highly effective in developing solutions to those problems
- Effective knowledge of the drug development process and the Theradex organizational structure
- Strong communication skills: verbal and written
- High level of proficiency in Microsoft Outlook, Word and Excel
- Candidate must be fluent in English.
What we offer:
Theradex is an equal opportunity employer. All qualified applicants are encouraged to apply and will receive consideration for employment.
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.
We offer a friendly and supportive culture that puts people first.
