CRAII/Senior CRA - SW England (Must have UK monitoring exp)
CRAII/Senior CRA - SW England (Must have UK monitoring exp)

CRAII/Senior CRA - SW England (Must have UK monitoring exp)

Farnborough Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Monitor clinical research studies, ensuring compliance and quality through on-site and remote evaluations.
  • Company: Syneos Health is a global leader in biopharmaceutical solutions, dedicated to accelerating customer success.
  • Benefits: Enjoy career development, a supportive culture, and the chance to make a real impact on patient lives.
  • Why this job: Join a passionate team that values diversity and innovation while improving healthcare outcomes worldwide.
  • Qualifications: Requires a Bachelor's degree and 5+ years of clinical research monitoring experience.
  • Other info: Embrace a culture where you can be your authentic self and grow your career.

The predicted salary is between 36000 - 60000 £ per year.

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, case report forms, and regulatory documents.
  • Develop tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and standard operating procedures.
  • Contribute to the design, implementation, and delivery of processes, programs, and policies by providing expert input and feedback during development and review stages.
  • Direct the work of lower-level professionals or manage processes and programs, including training and mentoring junior staff and overseeing their monitoring activities.
  • Ensure trials are conducted in accordance with regulatory requirements and company standards by performing regular audits and inspections, and addressing any compliance issues that arise.
  • Provide guidance and support to clinical research teams, including answering questions, resolving issues, and facilitating communication between team members and stakeholders.
  • Maintain accurate and timely documentation of monitoring activities, including writing detailed monitoring reports, tracking study progress, and updating databases.
  • Identify and resolve issues related to clinical trial conduct, such as protocol deviations, data discrepancies, and adverse events, and implement corrective and preventive actions as needed.
  • Collaborate with cross-functional teams to ensure successful trial execution, including working with project managers, data managers, biostatisticians, and regulatory affairs specialists.
Qualifications:
  • Bachelor's degree in a related field.
  • Minimum of 5 years of experience in clinical research monitoring; this role is a progression within the level from a Sr CRA II.
  • In-depth knowledge of clinical trial processes and regulations.
  • Strong analytical and problem-solving skills.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and as part of a team.
Certifications:

Certified Clinical Research Associate (CCRA) or equivalent certification preferred.

Necessary Skills:
  • Proficiency in clinical trial management systems and software.
  • Ability to manage multiple projects and priorities.
  • Strong attention to detail and organizational skills.
  • Ability to travel as required for on-site monitoring.
  • Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.

At Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. If your past experience doesn’t align perfectly, we encourage you to apply anyway. At times, we take into consideration transferable 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 those who need them most. A career with Syneos Health means your everyday work improves patients’ lives around the world.

CRAII/Senior CRA - SW England (Must have UK monitoring exp) employer: Syneos Health, Inc.

At Syneos Health, we pride ourselves on being an exceptional employer, offering a vibrant work culture that champions diversity and inclusion. Our commitment to employee growth is evident through comprehensive career development programmes, supportive management, and a Total Self culture that encourages authenticity. Located in Farnborough, our team collaborates in a dynamic environment where every role contributes to meaningful advancements in healthcare, making your work here impactful and rewarding.
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Contact Detail:

Syneos Health, Inc. Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land CRAII/Senior CRA - SW England (Must have UK monitoring exp)

✨Tip Number 1

Network with professionals in the clinical research field, especially those who have experience with UK monitoring. Attend industry events or join relevant online forums to connect with potential colleagues and learn about job openings.

✨Tip Number 2

Familiarise yourself with the latest regulations and guidelines related to clinical trials in the UK. Being knowledgeable about Good Clinical Practice (GCP) and local regulatory requirements will demonstrate your commitment and expertise during interviews.

✨Tip Number 3

Consider reaching out to current or former employees of Syneos Health on platforms like LinkedIn. They can provide insights into the company culture and the specific expectations for the CRAII/Senior CRA role, which can help you tailor your approach.

✨Tip Number 4

Prepare for potential interview questions by reviewing common scenarios faced in clinical monitoring. Think about how you would handle issues like protocol deviations or data discrepancies, as these are likely to come up in discussions.

We think you need these skills to ace CRAII/Senior CRA - SW England (Must have UK monitoring exp)

Clinical Trial Monitoring
Knowledge of Good Clinical Practice (GCP)
Regulatory Compliance
Analytical Skills
Problem-Solving Skills
Attention to Detail
Communication Skills
Interpersonal Skills
Project Management
Training and Mentoring
Documentation Skills
Ability to Manage Multiple Projects
Proficiency in Clinical Trial Management Systems
Collaboration with Cross-Functional Teams
Source Document Review

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant experience in clinical research monitoring, especially any UK-specific experience. Use keywords from the job description to demonstrate that you meet the qualifications.

Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of Syneos Health's mission. Mention specific experiences that align with the responsibilities listed in the job description.

Highlight Relevant Skills: In your application, emphasise your analytical skills, attention to detail, and ability to work both independently and as part of a team. Provide examples of how you've successfully managed multiple projects or resolved issues in past roles.

Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your professionalism and attention to detail, which are crucial in clinical research.

How to prepare for a job interview at Syneos Health, Inc.

✨Showcase Your UK Monitoring Experience

Since the role requires UK monitoring experience, be prepared to discuss specific examples from your past roles. Highlight any unique challenges you faced and how you overcame them, demonstrating your expertise in the local regulatory landscape.

✨Demonstrate Your Problem-Solving Skills

The job involves identifying and resolving issues related to clinical trials. Prepare to share instances where you successfully navigated complex problems, detailing your analytical approach and the outcomes of your actions.

✨Emphasise Team Collaboration

Syneos Health values collaboration across various teams. Be ready to discuss how you've worked with cross-functional teams in the past, focusing on your communication skills and how you facilitated effective teamwork to achieve project goals.

✨Prepare for Technical Questions

Given the technical nature of the role, brush up on your knowledge of clinical trial management systems and Good Clinical Practice (GCP) guidelines. Expect questions that assess your familiarity with these tools and regulations, and be ready to explain how you've applied them in your work.

CRAII/Senior CRA - SW England (Must have UK monitoring exp)
Syneos Health, Inc.
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  • CRAII/Senior CRA - SW England (Must have UK monitoring exp)

    Farnborough
    Full-Time
    36000 - 60000 £ / year (est.)

    Application deadline: 2027-07-18

  • S

    Syneos Health, Inc.

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