Find a job 
Featured Companies 
Featured Universities 
For Companies 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 flexible part-time hours, career development opportunities, and a supportive work culture.
- Why this job: Join a passionate team making a real impact on patient lives while developing your skills.
- Qualifications: Bachelor's degree and 5 years of clinical research monitoring experience required.
- Other info: This role offers a unique chance to lead and mentor junior staff in a dynamic environment.
Sr CRA II – Part time (18.75hr per week)
Sr CRA II – Part time (18.75hr per week)
3 weeks ago Be among the first 25 applicants
Description
Sr CRA II – Part time (18.75hr per week)
Description
Sr CRA II – Part time (18.75hr per week)
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 I
- 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
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
Part time CRA (0.5 FTE) Roles within Clinical Monitoring/CRA job family at the P22 level are responsible for monitoring clinical research studies to ensure that trials 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, who may manage two or fewer employees and direct the work of lower-level professionals or manage processes and programs. 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 Contribution Roles within Clinical Monitoring/CRA job family at the P22 level have a significant impact on the success of clinical research studies. They ensure that clinical projects are conducted, recorded, and reported in accordance with protocols, company and sponsor standard operating procedures (SOPs), ICH-GCP, and all applicable local and federal regulatory requirements. These roles contribute to the overall quality and integrity of clinical data, protect the confidentiality of subjects/patients, and assess factors that might affect subject/patient safety and clinical data integrity. They also provide recommendations regarding site-specific actions, communicate serious issues to the project team, and develop action plans. Additionally, these roles may assume clinical functional leadership tasks, act as primary liaison with study site personnel, and provide guidance at the site and project level towards audit readiness standards. Core Focus
- Ensure regulatory, ICH-GCP, and protocol compliance during site qualification, site initiation, interim monitoring, site management, and close-out visits
- Evaluate overall performance of site and site staff, provide recommendations regarding site-specific actions, and communicate serious issues to the project team
- Verify the process of obtaining informed consent, protect the confidentiality of subjects/patients, and assess factors affecting subject/patient safety and clinical data integrity
- Conduct Source Document Review, verify clinical data accuracy and completeness, and apply query resolution techniques
- Verify site compliance with electronic data capture requirements and investigational product (IP) inventory, reconciliation, storage, and security
- Review Investigator Site File (ISF) for accuracy, timeliness, and completeness, and reconcile contents with the Trial Master File (TMF)
- Document activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents
- Manage site-level activities and communication to ensure project objectives, deliverables, and timelines are met
- Act as primary liaison with study site personnel, ensure training and compliance with applicable requirements, and provide guidance towards audit readiness standards
- Provide direct supervision, training, and mentorship to junior level CRAs
Seniority level
-
Seniority level
Mid-Senior level
Employment type
-
Employment type
Full-time
Job function
-
Job function
Research and Science
-
Industries
Biotechnology Research, Pharmaceutical Manufacturing, and Research Services
Referrals increase your chances of interviewing at Syneos Health by 2x
Get notified about new Senior Clinical Research Associate jobs in England, United Kingdom.
Twickenham, England, United Kingdom 15 hours ago
London, England, United Kingdom 6 days ago
Senior Research Manager – Infrastructure Monitoring and Evaluation
London, England, United Kingdom 1 week ago
Greater London, England, United Kingdom 3 days ago
Associate Director, Clinical Trial Manager
City Of London, England, United Kingdom £38,000.00-£45,000.00 3 days ago
Bracknell, England, United Kingdom 3 weeks ago
Addlestone, England, United Kingdom 2 weeks ago
Addlestone, England, United Kingdom 2 weeks ago
Senior Manager, Pharmacovigilance – UK/EU – Remote
Clinical Trial Manager – Oncology – UK – Remote
Clinical Research Fellow [Clinical Research Associate] (Fixed Term)
Cambridge, England, United Kingdom 6 days ago
Bollington, England, United Kingdom 5 days ago
12 Month – Local Trial Manager – FSP – Remote
Uxbridge, England, United Kingdom 1 week ago
London, England, United Kingdom 2 hours ago
Senior Translational Research Manager – Maternity Leave
London, England, United Kingdom 2 weeks ago
Senior Translational Research Manager – Maternity Leave
Associate Clinical Data Manager – Early Phase Trials
Maidenhead, England, United Kingdom 3 days ago
Clinical and Translational Research Program Manager
Stevenage, England, United Kingdom 10 hours ago
Little London, England, United Kingdom 1 week ago
Abingdon-On-Thames, England, United Kingdom 3 days ago
London, England, United Kingdom 2 hours ago
Associate Project Manager, Decentralised Clinical Trials
London, England, United Kingdom 5 days ago
Manchester, England, United Kingdom 1 week ago
Stevenage, England, United Kingdom 2 hours ago
London, England, United Kingdom 1 week ago
Hartley Wintney, England, United Kingdom 1 week ago
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr
Sr CRA II - Part time (18.75hr per week) employer: Syneos Health
Contact Detail:
Syneos Health Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Sr CRA II - Part time (18.75hr per week)
✨Tip Number 1
Familiarise yourself with the latest clinical trial regulations and Good Clinical Practice (GCP) guidelines. This knowledge will not only help you in interviews but also demonstrate your commitment to maintaining high standards in clinical research.
✨Tip Number 2
Network with current or former employees of Syneos Health on platforms like LinkedIn. Engaging with them can provide valuable insights into the company culture and expectations, which can be a great advantage during the interview process.
✨Tip Number 3
Prepare specific examples from your past experience that showcase your problem-solving skills and ability to manage multiple projects. Highlighting these competencies will align well with the responsibilities outlined in the job description.
✨Tip Number 4
Stay updated on recent developments in the biopharmaceutical industry. Being knowledgeable about current trends and challenges can help you engage in meaningful discussions during interviews, showing your passion for the field.
We think you need these skills to ace Sr CRA II - Part time (18.75hr per week)
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 certifications you hold, such as CCRA.
Craft a Strong Cover Letter: In your cover letter, express your passion for clinical research and how your skills align with the responsibilities outlined in the job description. Mention specific experiences that demonstrate your problem-solving abilities and teamwork.
Highlight Relevant Skills: Clearly outline your analytical and organisational skills in your application. Provide examples of how you've successfully managed multiple projects or resolved compliance issues in previous roles.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in clinical research.
How to prepare for a job interview at Syneos Health
✨Know Your Clinical Research Basics
Make sure you have a solid understanding of clinical trial processes, regulations, and Good Clinical Practice (GCP) guidelines. Brush up on your knowledge of the specific protocols and compliance requirements that Syneos Health adheres to, as this will show your preparedness and commitment.
✨Demonstrate Problem-Solving Skills
Be ready to discuss past experiences where you've identified and resolved issues in clinical trials. Highlight your analytical skills and how you've implemented corrective actions in previous roles, as this is crucial for the Sr CRA II position.
✨Showcase Your Communication Abilities
Effective communication is key in this role. Prepare examples of how you've facilitated communication between team members and stakeholders in past projects. This will demonstrate your ability to work collaboratively and support clinical research teams.
✨Prepare Questions for Your Interviewers
Think of insightful questions to ask about the company culture, team dynamics, and expectations for the Sr CRA II role. This not only shows your interest in the position but also helps you assess if Syneos Health is the right fit for you.
