Clinical Data Reviewer - Internal Medicine (US, CAN, UK Only)

Clinical Data Reviewer - Internal Medicine (US, CAN, UK Only) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. 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 deliver—for one another, our customers, and, most importantly, for those in need. Job Responsibilities Clinical Monitoring background is required. Internal Medicine experience is required. Must be located in US, CAN, or UK with no sponsorship needs to be considered for this role. Ensure data readiness for important milestones including, but not limited to, 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. reviewing to identify inconsistencies in the participant's data). Generate queries on discrepant data and follow 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 any safety signals. May identify protocol deviations during routine clinical review and escalation as appropriate. Follow relevant SOPs and regulations, have an excellent understanding of and comply with applicable training requirements, constantly seeking further improvements in quality and efficiency of clinical procedures. May liaise with data management, clinical and site management along with other members of the study team. Attend Clinical Meetings and Study Meetings, as necessary. Qualifications Bachelor's degree or nursing degree is preferred. At least 7 years of clinical research experience in the pharmaceutical industry (Strong monitoring experience is a plus). Background in clinical monitoring or RN strongly preferred. 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 format (filter, sort, data format (date)). 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 (i.e. fluid, flexible work style). Possess basic knowledge of data management including case report form design, workings of electronic edit checks, implementation of data handling conventions and interpretation of data status reports. Good written and oral communication skills with strong attention to detail required. Benefits The benefits for this position may include a company car or car allowance, health benefits to include medical, dental, and vision, company match 401k, eligibility to participate in employee stock purchase plan, eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements. Salary Range $80,600.00 - $145,000.00. The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role. 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. #J-18808-Ljbffr Syneos Health/ inVentiv Health Commercial LLC