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- Tasks: Monitor clinical research studies, ensuring compliance and quality through on-site and remote assessments.
- Company: Syneos Health is a leading biopharmaceutical solutions organisation dedicated to accelerating customer success.
- Benefits: Enjoy a supportive culture, career development opportunities, and the chance to work remotely.
- Why this job: Make a real impact on patient lives while collaborating with passionate problem solvers in a diverse environment.
- Qualifications: Bachelor's degree or equivalent experience; 2-4 years in clinical research monitoring required.
- Other info: Join a global team of 29,000 employees committed to making a difference in healthcare.
The predicted salary is between 36000 - 60000 ÂŁ per year.
Unblinded CRA II/Senior CRA – UK only – Sponsor dedicated
Updated: Yesterday
Location: GBR-Remote
Job ID:25101234
Description
Unblinded CRA II/Senior CRA – UK only – Sponsor dedicated
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health
- We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
- We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.
Job Responsibilities
- Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms
- Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates
- Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials
- Manage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues
- Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and action plans
- Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct
Qualifications:
- Bachelor\’s degree in a related field or equivalent experience
- Minimum of 2-4 years of experience in clinical research monitoring
- Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements
- Excellent communication and interpersonal skills
- Ability to work independently and manage multiple priorities
- Proficiency in using clinical trial management systems and other relevant software
Certifications:
- Certified Clinical Research Associate (CCRA) or equivalent certification preferred
Necessary Skills:
- Attention to detail and strong analytical skills
- Problem-solving abilities and critical thinking
- Ability to work effectively in a team environment
- Strong organizational and time management skills
- Proficiency in Microsoft Office Suite
Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
http://www.syneoshealth.com
Additional Information
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Summary
Roles within Clinical Monitoring/CRA job family at the P21 level are responsible for ensuring that clinical research studies are conducted in accordance with widely accepted clinical practices. This includes conducting on-site and remote monitoring, developing tools, procedures, and processes to ensure quality monitoring. These roles involve individual contributors with responsibility in a professional or technical discipline or specialty, and may manage two or fewer employees. The majority of time is spent contributing to the design, implementation, or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education.Impact and ContributionRoles within Clinical Monitoring/CRA job family at the P21 level have a significant impact on the quality and integrity of clinical research studies. By ensuring adherence to clinical practices and protocols, these roles contribute to the reliability and validity of study results. They play a crucial role in the development and implementation of monitoring tools and procedures, which enhance the overall efficiency and effectiveness of clinical trials. Their contributions are essential for advancing medical knowledge and improving patient outcomes.Core Focus• Conduct thorough on-site and remote monitoring of clinical research studies• Develop and implement tools, procedures, and processes to ensure quality monitoring• Manage defined components of projects or processes within their area of responsibility• Utilize practical knowledge of a professional area, typically obtained through education combined with experience• Maintain high standards of clinical practice and ensure the success of clinical trials
At Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. If your pastexperience doesn’t align perfectly, we encourage you to apply anyway. At times, we take intoconsideration transferrable skills from previous roles. We also encourage you to join our Talent Network to stay connected to additional career opportunities.
Discover what our 29,000 employees already know: work here matters everywhere. We work hard,and smart, all in the name of getting much-needed therapies to thosewho need them most. A career with Syneos Health means your everyday work improvespatients’ lives around the world. Selecting us as an employer secures a career inwhich you’re guaranteed to:
Syneos Health (Nasdaq: SYNH) is a leading integrated biopharmaceutical solutionsorganization built to accelerate customer success. We translate unique clinical,medical affairs and commercial insights into outcomes to address modern marketrealities. Together we share insights, use the latest technologies and applyadvanced business practices to speed our customers’ delivery of importanttherapies to patients. We support a diverse, equitable and inclusive culture.
Phone: 919 876 9300
Fax: 919 876 9360
Toll-Free: 866 462 7373
Syneos Health is an Equal Opportunity Employer. All qualified applicants will receiveconsideration for employment without regard to race, color, age, religion, marital status,ethnicity, national origin, sex, gender, gender identity, sexual orientation, protectedveteran status, disability or any other legally protected status and will not bediscriminated against. If you are an individual with a disability who requires reasonableaccommodation to complete any part of our application process, including the use of thiswebsite, please contact us at: Email: jobs@syneoshealth.com One of our staff members will workwith you to provide alternate means to submit your application.
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Unblinded CRA II/Senior CRA - UK only - Sponsor dedicated employer: Syneos Health, Inc.
Contact Detail:
Syneos Health, Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Unblinded CRA II/Senior CRA - UK only - Sponsor dedicated
✨Tip Number 1
Familiarise yourself with Good Clinical Practice (GCP) guidelines and regulatory requirements. This knowledge is crucial for a CRA role, and being able to discuss these during your interview will demonstrate your expertise and commitment to quality in clinical research.
✨Tip Number 2
Network with professionals in the clinical research field, especially those who work at Syneos Health or similar organisations. Attend industry events or join relevant online forums to make connections that could lead to referrals or insider information about the role.
✨Tip Number 3
Prepare to discuss specific examples of how you've managed multiple priorities in previous roles. Highlighting your organisational and time management skills will show that you can handle the demands of a CRA position effectively.
✨Tip Number 4
Research Syneos Health's recent projects and initiatives. Being knowledgeable about their work will not only help you tailor your responses during the interview but also demonstrate your genuine interest in the company and its mission.
We think you need these skills to ace Unblinded CRA II/Senior CRA - UK only - Sponsor dedicated
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research monitoring. Emphasise your knowledge of Good Clinical Practice (GCP) guidelines and any specific software you’ve used in previous roles.
Craft a Strong Cover Letter: Write a cover letter that clearly outlines your motivation for applying to Syneos Health. Mention how your skills align with the job responsibilities, such as conducting monitoring activities and collaborating with cross-functional teams.
Highlight Relevant Experience: In your application, focus on your past roles that involved clinical trial monitoring. Provide specific examples of how you ensured compliance with clinical practices and contributed to the development of monitoring tools or procedures.
Showcase Soft Skills: Syneos Health values strong communication and problem-solving abilities. Make sure to include examples that demonstrate your interpersonal skills and ability to manage multiple priorities effectively.
How to prepare for a job interview at Syneos Health, Inc.
✨Know Your GCP Guidelines
Make sure you have a solid understanding of Good Clinical Practice (GCP) guidelines. Be prepared to discuss how you've applied these principles in your previous roles, as this will demonstrate your expertise and commitment to quality monitoring.
✨Showcase Your Problem-Solving Skills
During the interview, be ready to share specific examples of challenges you've faced in clinical research monitoring and how you resolved them. This will highlight your analytical skills and ability to think critically under pressure.
✨Familiarise Yourself with Their Processes
Research Syneos Health's approach to clinical trials and their Total Self culture. Understanding their values and processes will allow you to tailor your responses and show that you're genuinely interested in being part of their team.
✨Prepare for Team Collaboration Questions
Expect questions about teamwork and collaboration, as these are crucial in clinical research. Think of examples where you've successfully worked with cross-functional teams and how you contributed to achieving common goals.
