At a Glance
- Tasks: Review clinical data to ensure accuracy and compliance for oncology studies.
- Company: Join a leading pharmaceutical company dedicated to improving patient outcomes.
- Benefits: Enjoy health benefits, flexible PTO, and a company car or allowance.
- Other info: Opportunity for career growth and professional development in a supportive environment.
- Why this job: Make a real difference in cancer research while working remotely with a dynamic team.
- Qualifications: 7+ years in clinical research with strong data review skills required.
The predicted salary is between 60000 - 75000 € per year.
Location: United States, Canada, United Kingdom. Candidates must reside in one of these countries and have no sponsorship needs.
Job Responsibilities
- Ensure data readiness for important milestones including interim analysis, final analysis, snapshots to support submissions, Data Monitoring Committee reviews, and publications.
- Review participant level data across a study in adherence with CRF Completion guidelines (CCGs) and the Data Review Plan (DRP).
- Conduct point‑to‑point data checks (e.g., verifying the presence of a lab test that satisfies study inclusion criteria) and interpretive analysis (e.g., identifying inconsistencies in participant data).
- Generate queries on discrepant data and follow up to resolution, including escalation of issues that cannot be resolved through the query process.
- Create and use data review best practices and associated data review tools to identify trends and safety signals.
- May identify protocol deviations during routine clinical review and escalation as appropriate.
- Follow relevant SOPs and regulations, comply with training requirements, and seek continuous improvements in quality and efficiency of clinical procedures.
- May liaise with data management, clinical, and site management along with other study team members.
- Attend clinical meetings.
Qualifications
- Bachelor’s degree or nursing degree preferred.
- At least 7 years of clinical research experience in the pharmaceutical industry; strong monitoring experience is a plus.
- Direct clinical review and query writing/resolution experience required.
- Possess sufficient clinical knowledge to assess if participant data is scientifically and clinically valid.
- Prior EDC experience preferred.
- Proficient in reviewing large‑scale listings in Microsoft Excel (filter, sort, data format).
- Basic understanding of how data points from different fields/CRFs interact and how data collection impacts analysis.
- Ability to work independently in a virtual setting and as part of a remote team.
- Ability to prioritize and adjust work priorities quickly as needed to meet deadlines (fluid, flexible work style).
- Possess basic knowledge of data management including case report form design, electronic edit checks, data handling conventions, and interpretation of data status reports.
- Good written and oral communication skills with strong attention to detail.
Benefits
- Company car or car allowance.
- Health benefits (Medical, Dental, Vision).
- Company match 401(k).
- Employee Stock Purchase Plan eligibility.
- Eligibility to earn commissions/bonuses based on company and individual performance.
- Flexible paid time off (PTO) and sick time (subject to local regulations).
Salary Range: The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on qualifications, skills, and proficiency for the role.
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. All employment decisions are made in accordance with applicable federal, state, and municipal laws, including the EU Equality Directive, to ensure equal employment opportunity.
Clinical Data Reviewer - Oncology Required (US, CAN, UK Only) employer: Syneos Health
At Syneos Health, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the field of oncology clinical research. Our employees benefit from comprehensive health plans, flexible paid time off, and opportunities for professional growth, all while working in a supportive environment that values diversity and inclusion. With a commitment to employee well-being and career development, Syneos Health stands out as a rewarding place to advance your career in clinical data review.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Data Reviewer - Oncology Required (US, CAN, UK Only)
✨Tip Number 1
Network like a pro! Reach out to professionals in the oncology field on LinkedIn or at industry events. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your clinical data knowledge. Be ready to discuss your experience with data review and query resolution, as well as how you handle discrepancies. We want to see your expertise shine!
✨Tip Number 3
Showcase your skills with a portfolio! If you've got examples of your work, like data review tools or best practices you've developed, bring them along to interviews. It’s a great way to demonstrate your hands-on experience.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Clinical Data Reviewer - Oncology Required (US, CAN, UK Only)
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Data Reviewer role. Highlight your relevant experience in clinical research, especially any work related to oncology. We want to see how your skills match what we're looking for!
Showcase Your Skills:In your application, don’t just list your qualifications—show us how you’ve used them! Talk about your experience with data review, query writing, and any tools you've used. This helps us see your practical knowledge in action.
Be Clear and Concise:When writing your application, keep it clear and to the point. Use straightforward language and avoid jargon unless it's relevant. We appreciate a well-structured application that’s easy to read!
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’s super easy to do!
How to prepare for a job interview at Syneos Health
✨Know Your Data Inside Out
Make sure you’re familiar with the types of data you’ll be reviewing. Brush up on CRF Completion guidelines and the Data Review Plan. Being able to discuss specific examples of how you've handled data discrepancies in the past will show your expertise.
✨Showcase Your Clinical Knowledge
Prepare to demonstrate your understanding of clinical research and participant data validity. Think about scenarios where you identified protocol deviations or resolved complex queries, and be ready to share these experiences during the interview.
✨Excel Skills are Key
Since you'll be working with large-scale listings in Microsoft Excel, practice your skills beforehand. Be prepared to discuss how you filter, sort, and format data, as well as any tools or techniques you use to identify trends and safety signals.
✨Communicate Clearly and Confidently
Good communication is crucial in this role. Practice articulating your thoughts clearly, especially when discussing technical details. Remember, it’s not just about what you say, but how you say it—confidence can make a big difference!