At a Glance
- Tasks: Lead clinical trials, ensuring safety and compliance while supporting site personnel.
- Company: Sitero, a leader in innovative clinical services and software solutions.
- Benefits: Competitive salary, flexible part-time hours, healthcare, and retirement benefits.
- Other info: Join a diverse team committed to ethics and innovation in clinical research.
- Why this job: Make a real impact in life sciences while working with cutting-edge technology.
- Qualifications: Bachelor's degree in science and 3 years of independent monitoring experience required.
The predicted salary is between 36000 - 60000 £ per year.
Overview
Siterois an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our experienced team delivers high-touch services and technology to ensure the safety of all stakeholders across the clinical research community with an emphasis on ethics, compliance, and innovation.
Job Title and Location
Job Title: Senior CRA (Contractor)
Location: United Kingdom
Function: Clinical Operations
Mandatory Experience: At least 3 years of independent monitoring experience with a CRO
Responsibilities
- Primary point of contact for site personnel during life cycle of clinical trial. This includes study start up support, site activation, trial conduct and closeout of a clinical trial.
- Provides support to the Global Project Lead and CTM during project start up to ensure timely site selection and feasibility. Assists with collection of essential documents from the site. May assist with submission of central EC Applications, Local EC applications, RA applications and any other local regulatory applications/Approvals required.
- Ability to identify protocol deviations and pharmacovigilance issues that might affect data accuracy or patient safety.
- Conduct Site qualification, site initiation, routine site monitoring close out visits (remote and onsite), Central monitoring in compliance with study protocol and ICH-GCP.
- Expert documentation of monitoring priorities/activities via site visit confirmation and follow up letters, monitoring visit reports, and any trial associated logs.
- Oversees conduct trials by reviewing study data listings, vendor dashboards, and CTMS issues/actions documentation to identify trends, errors, and any potential breeches that can impact data integrity.
- Ability to present essential function of CRA role in Bid Defenses, Investigator Meetings, and Sponsor Face to Face meetings.
- Assists the Global Project Lead in identification of out-of-scope activities.
- Basic understanding of assigned projects scope, milestones and budget and manages site level activities to ensure project deliverables are met.
- Provides support to the CTM and Global project lead in negotiation of site budgets and contracts.
Education and Experience Required
- Bachelors degree in a science or life science related field required
- 3 years minimum of independently monitoring drug trials
- Experience in GI or Urology required
Compensation & Benefits
Siteroproudly offers animpressive compensation package and benefits, including a competitive salary, Variable pay, paid time off, and healthcare and retirement benefits.
Employment Type
Part Time, Contractor
Commitments
- Part Time hours flexible to the study requirements
- Willing to work in shifts as and when needed.
Disclaimer
Siterois an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive consideration for employment without discrimination on the basis of race,color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.
Senior Clinical Research Associate (Contractor) employer: Sitero LLC
Sitero is an exceptional employer, offering a dynamic work environment that prioritises innovation and ethical practices in clinical research. With a strong focus on employee growth, Sitero provides comprehensive training and development opportunities, ensuring that team members can thrive in their careers while contributing to meaningful advancements in life sciences. Located in the United Kingdom, the company fosters a collaborative culture that values flexibility and work-life balance, making it an ideal place for professionals seeking rewarding and impactful employment.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Clinical Research Associate (Contractor)
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online groups. We all know that sometimes it’s not just what you know, but who you know that can help you land that Senior CRA role.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ICH-GCP guidelines and recent trends in clinical trials. We want you to be able to showcase your expertise confidently, so practice answering common CRA interview questions and think about how your experience aligns with Sitero's innovative approach.
✨Tip Number 3
Don’t forget to follow up after interviews! A quick thank-you email can go a long way in showing your enthusiasm for the position. We recommend mentioning something specific from your conversation to remind them why you’re the perfect fit for their team.
✨Tip Number 4
Apply through our website for the best chance at landing that contract role. We make it easy for you to showcase your skills and experience directly to our hiring team. Plus, it shows you’re genuinely interested in being part of the Sitero family!
We think you need these skills to ace Senior Clinical Research Associate (Contractor)
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior CRA role. Highlight your independent monitoring experience and any specific therapeutic areas you've worked in, like GI or Urology. We want to see how your background aligns with what we do!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your skills can contribute to our innovative approach at Sitero. Keep it concise but impactful!
Showcase Your Achievements:When detailing your experience, focus on your achievements rather than just responsibilities. Did you improve data accuracy or streamline processes? We love to see how you've made a difference in your previous roles!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at Sitero LLC
✨Know Your Stuff
Make sure you brush up on your clinical research knowledge, especially around GI and Urology. Be ready to discuss your independent monitoring experience in detail, as this will be crucial for the role.
✨Showcase Your Communication Skills
As a Senior CRA, you'll be the primary contact for site personnel. Practice articulating how you've effectively communicated with stakeholders in past projects, especially during study start-up and closeout phases.
✨Prepare for Scenario Questions
Expect questions about how you'd handle protocol deviations or pharmacovigilance issues. Think of specific examples from your experience where you identified and resolved such challenges, demonstrating your problem-solving skills.
✨Understand the Company’s Values
Familiarise yourself with Sitero's focus on ethics, compliance, and innovation. Be prepared to discuss how your personal values align with theirs and how you can contribute to their mission in the life sciences industry.
