At a Glance
- Tasks: Monitor and manage clinical studies, ensuring compliance with protocols and regulations.
- Company: Join Precision for Medicine, a passionate CRO focused on innovative cancer therapies.
- Benefits: Enjoy remote work, a supportive culture, and a healthy work/life balance.
- Why this job: Make a real impact in oncology research while being valued for your contributions.
- Qualifications: A degree and at least 1 year of CRA experience are required; oncology experience is a plus.
- Other info: This role is fully home-based in the UK with reasonable travel commitments.
The predicted salary is between 36000 - 60000 £ per year.
Overview
Precision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages. CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will have a lower than average number of protocols, setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully – your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.
Position: Clinical Research Associate II, this position will be fully home based working in the UK.
About You
- You are calm, thoughtful, and responsive when things don’t go as planned.
- You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
- You find quick and creative ways of overcoming difficulties.
- You have an impeccable eye for detail.
- You identify potential study risks and propose solutions on how to mitigate them.
- You take responsibility in the quality and outcomes of your work.
- You are adept at handling conflict by using tried and true resolution strategies.
How we will keep you busy and support your growth
You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
Qualifications
Minimum Required:
- 4-year college degree or equivalent experience
Other Required:
- Candidates should ideally have more than 1 year CRA experience within the CRO or pharmaceutical industry.
- Oncology experience, early phase experience desirable although not essential.
- Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions).
- Fluency in English.
Privacy and Equal Opportunity
Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.
It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.
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Clinical Research Associate II employer: Precision For Medicine
Contact Detail:
Precision For Medicine Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate II
✨Tip Number 1
Familiarise yourself with the specific protocols and procedures used in oncology studies. Understanding the nuances of these protocols will not only help you during interviews but also demonstrate your commitment to the role.
✨Tip Number 2
Network with current or former Clinical Research Associates at Precision for Medicine. Engaging with them can provide insights into the company culture and expectations, which can be invaluable during your application process.
✨Tip Number 3
Prepare to discuss your problem-solving strategies in detail. Given the emphasis on overcoming difficulties in the job description, having specific examples ready will showcase your ability to handle challenges effectively.
✨Tip Number 4
Highlight your experience with regulatory submissions and site visits in conversations. This is crucial for a CRA II role, and demonstrating your expertise in these areas can set you apart from other candidates.
We think you need these skills to ace Clinical Research Associate II
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience, especially any previous roles as a Clinical Research Associate. Emphasise your skills in monitoring clinical studies, attention to detail, and any oncology experience you may have.
Craft a Compelling Cover Letter: Write a cover letter that reflects your passion for clinical research and your understanding of Precision for Medicine's mission. Mention how your calm and thoughtful approach aligns with their values and how you can contribute to their culture.
Showcase Problem-Solving Skills: In your application, provide examples of how you've overcome challenges in previous roles. Highlight your ability to identify risks and propose effective solutions, as this is crucial for the CRA II position.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is essential for a Clinical Research Associate.
How to prepare for a job interview at Precision For Medicine
✨Show Your Passion for Oncology
Make sure to express your enthusiasm for oncology and precision medicine during the interview. Discuss any relevant experiences or projects that highlight your interest in this field, as it aligns with the company's mission.
✨Demonstrate Problem-Solving Skills
Prepare examples of how you've creatively overcome challenges in previous roles. This will showcase your ability to think on your feet and handle unexpected situations, which is crucial for a Clinical Research Associate.
✨Highlight Attention to Detail
Since the role requires an impeccable eye for detail, be ready to discuss specific instances where your attention to detail made a significant impact on a project. This could include identifying risks or ensuring compliance with protocols.
✨Prepare for Behavioural Questions
Expect questions about how you handle conflict and work within a team. Use the STAR method (Situation, Task, Action, Result) to structure your responses, demonstrating your calm and thoughtful approach to problem-solving.