Senior Clinical Trial Analytics Monitor I
$100k - $120kEverest Clinical Research
Senior Clinical Trial Analytics Monitor I
Everest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.
Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest's headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Bridgewater (Greater New York City Area), New Jersey, USA, Shanghai (Pudong Zhangjiang New District), China and Taipei, Taiwan.
Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients' needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.
Quality is our backbone, customer-focus is our tradition, flexibility is our strength…that's us…that's Everest.
To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Senior Clinical Trial Analytics Monitor I for our Toronto/Markham, Ontario, Canada on-site location, or remotely from a home-based office anywhere in Canada in accordance with our Work from Home policy.
Key Accountabilities:
- Partner with stakeholders across various business units (Clinical Operations, Medical Affairs, Data Management, Statistics, and Project Management, etc.) to gather reporting requirements and ensure alignment on data reporting needs and priorities.
- Act as a bridge between CTT technical teams and Sponsor/Everest teams to ensure reporting solutions are accurate and insightful.
- Lead the collection and documentation of Library reporting needs across departments to identify overlaps and standardization opportunities.
- Define and enforce consistent metrics, KPIs, and business definitions to ensure comparability and clarity across indications.
- Design and develop interactive dashboards and standardized reports using BI tools (e.g., Spotfire, Medidata CDS, etc.).
- Build scalable and repeatable reporting solutions that serve the broader needs of the organization.
- Ensure data accuracy and consistency across reports by validating sources, applying proper transformations, and performing quality checks.
- Collaborate with CTT developers and IT to troubleshoot and resolve data issues impacting report integrations.
- Contribute to the establishment and enforcement of BI reporting standards, naming conventions, and documentation practices.
- Maintain a central repository of standard reports and dashboards for enterprise-wide access and visibility.
- Track and analyze key performance indicators (KPIs) to support data-driven decision-making across business units.
- Proactively identify trends, anomalies, and opportunities for improvement through reporting outputs.
Qualifications and Experience:
- A bachelor's degree in health science, physical or biological fields, or computer science.
- At least five years of experience in clinical research data analytics and BI reporting implementation.
- At least four or more years of experience in programming languages SQL, PL/SQL, R, Python or SAS.
- Experience in development and maintenance of enterprise clinical data standards.
- Ability to think on the spot and apply critical thinking skills to triage user issues and formulate optimal responses.
- Ability to effectively and appropriately interact with clients and Everest internal staff via telephone and written email communications.
- At least four or more years of experience in clinical trial data processing, technology delivery, process analysis and design, software development lifecycle, software testing, and project management.
- Experience with client relationship management.
- Comfortable using web application technologies and has prior customer service/support experience.
- Comfortable with technology and web-based tools.
- Aptitude to learn and retain CTT CDD application rules and support procedures and broader related clinical trials processes to effectively troubleshoot and support user inquiries.
- Adaptive to varying customer knowledge and skill levels (patience).
- Adhere to all company security and privacy standards, and other policies and SOPs.
- Good organizational skills and the ability to handle multiple tasks.
Benefits & Compensation:
We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage, life & AD&D insurance, short- and long-term disability, tuition reimbursement, fitness reimbursement, employee assistance program (EAP), a pension plan, generous paid time off and sick leave, and the opportunity to earn a performance based bonus.
Estimated Salary Range: $100,000 - $120,000
$135k - $165k
Overview The Senior Manager will be responsible for... ...overall oversight of clinical studies, ensuring the... ...integrity of risk-based monitoring deliverables. This involves... ...with Clinical Trial Managers (CTMs) to detail... ...critical system reports or analytics (e.g., central...SeniorFull timeLocal areaRemote work$110.52k - $138.15k
...ICON is seeking a Senior Clinical Research Associate to manage oncology clinical trials in Rochester, NY. You will engage with key sites, ensuring data integrity through monitoring and training while fostering compliance and strong relationships with site staff. This...Senior- ...Worldwide Clinical Trials Limited is seeking a Clinical Research Associate based in the Town of Belgium, Wisconsin, to manage site qualifications and monitor various clinical studies. Candidates should possess 5+ years of relevant experience, especially in Oncology, Hematology...SeniorWorldwide
$108k - $153k
...Edwards Lifesciences seeks a Clinical Affairs professional in Irvine, California. The role involves field monitoring, quality assurance, and regulatory compliance for clinical trials. Candidates should hold a Bachelor's Degree and have 5 years of related experience, with...Senior- ...Scorpion Therapeutics in New Jersey is seeking a CRA/Sr. CRA to ensure quality in clinical trial management and compliance. The successful candidate will oversee monitoring activities, safeguard patient rights, and ensure data integrity across various phases of trials...SeniorRemote workFlexible hours
$85k - $125k
...A clinical research organization in Bethesda, MD is seeking a Central Monitor to oversee risk-based quality management in clinical trials. Candidates should have a strong background in regulatory requirements and a minimum of 3 years in centralized monitoring. Responsibilities...Senior- ...Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) based in Washington, D.C. The Sr. CRA will oversee site management and monitoring, ensuring patient safety and quality execution of clinical trials. Key responsibilities include conducting clinical trial...Senior
- ...NCBiotech in Durham, North Carolina, is seeking a passionate Clinical Research Associate (CRA) to deliver high-quality clinical trials. You will lead site monitoring visits, ensuring adherence to GCP/ICH guidelines while building strong relationships with investigative...Senior
- ...Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to oversee site management and monitoring of clinical trials in Indianapolis, Indiana. Responsibilities include ensuring patient safety, managing site relationships, and resolving protocol-related issues...Senior
- ...IQVIA in Arizona is seeking a Clinical Research Associate (CRA) to lead clinical trials while ensuring compliance and high-quality execution. This role involves... ...field and have at least 1.5 years of on-site monitoring experience. Join us to make a direct impact on advancing...Senior
- ...Novartis Group Companies is seeking an SSO Field Monitoring Area Head to lead clinical trial execution across the United States. This role is crucial for driving field strategy, optimizing site engagement, and ensuring quality in trial delivery. Ideal candidates will...Senior
$145k - $175k
...A leading Clinical Research Organization in Los Angeles is seeking a Senior Contract Oncology Clinical Research Associate (SCRA) to monitor ongoing clinical trials. You will conduct both remote and on-site monitoring, participate in developing study tools and protocols...SeniorContract workRemote work$79.72k - $119.58k
...Description The Senior Clinical Research Monitor is responsible for performing ongoing internal reviews of research projects where human subject... ...documents (investigational product compliance) for IRB approved trials conducted by Tisch Cancer Institute. Conducts exit...SeniorTraineeshipRemote work- ...IQVIA LLC is seeking a Sr. Clinical Research Associate to monitor and manage oncology clinical trial sites in Overland Park, KS. This role involves key responsibilities such as conducting site monitoring visits, ensuring compliance with regulations, and managing subject...Senior
- ...Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) in Boston, MA. The Sr. CRA will manage and monitor clinical trial sites to ensure patient safety, compliance with regulations, and quality execution of clinical studies. This role involves extensive site...Senior
- ...Parexel seeks a Senior Clinical Research Associate in Richmond, Virginia, to oversee clinical... ...with ICH-GCP, and performing site monitoring. The ideal candidate will bring over 5... ...oncology. The position demands strong analytical skills and the ability to work collaboratively...SeniorRemote work
- Parexel is seeking a Senior Clinical Research Associate (SrCRA) in Boston, MA, responsible for site monitoring and management activities for sponsored studies. The SrCRA will... ...experience required, the role mandates strong analytical and communication skills, along with a...Senior
- ...Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) in Annapolis, Maryland, to manage clinical trials. You'll ensure adherence to Good Clinical Practices (GCP) and... ...image through effective site management and monitoring. The ideal candidate will have a Bachelor...Senior
- Fred Hutchinson Cancer Center (Fred Hutch) is seeking a Clinical Research Monitor II to support quality and compliance in oncology clinical trials in Seattle. Candidates should have a Bachelor's degree and at least 7 years of clinical research monitoring experience, preferably...Senior
- ...Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to manage site monitoring and ensure quality execution of clinical trials in Minnesota. The role involves ensuring compliance with regulations and maintaining site relationships. The ideal candidate has...Senior
$160k - $200k
...life sciences recruitment firm is seeking a Sr. Field Clinical Research Associate to monitor clinical studies and ensure regulatory compliance. Ideal... ...experience. This role requires strong communication and analytical skills, with a remote work option available that...SeniorRemote job- Parexel is seeking a Senior Clinical Research Associate in Albany, NY, to manage site operations for clinical trials ensuring compliance with regulations. This role involves overseeing trial sites, monitoring patient safety, and liaising between investigators and study...Senior
- ...Parexel International is seeking a Senior Clinical Research Associate (SrCRA) for local responsibilities... ...in study delivery. The role involves monitoring clinical study sites, ensuring... ...possesses strong communication and analytical skills. The position requires a bachelor...SeniorLocal areaRemote work
- WCT Worldwide Clinical Trials GER GmbH is seeking a Clinical Research Associate (CRA) based in the United States, Ohio. The CRA will support clinical research, ensuring site qualification and monitoring. Responsibilities include mentoring other CRAs, conducting site visits...SeniorWork at officeWorldwide
- ...Medical Monitor Position Responsibilities Perform medical monitoring work with a larger portion as a global/program level medical... ...& Experience: Medically qualified with experience in clinical practice. Experience in global medical monitoring and program...SeniorWork at officeRemote work
- Parexel is seeking a Senior Clinical Research Associate (SrCRA) responsible for supporting monitoring and site management activities for clinical trials. This role involves collaboration with clinical... .... Strong communication and analytical skills are essential. The...Senior
- ...type of cancer; innovative therapies and clinical trials; comprehensive patient and family... ...is seeking qualified candidates for the Senior Administrator, DSMC. Position details are... ...Senior Administrator, Data Safety and Monitoring Committee (DSMC) at Winship supports and...SeniorLocal area
- Parexel in Columbus, Ohio is seeking a Senior Clinical Research Associate to oversee the site management, monitoring, and close-out of clinical trials. The ideal candidate will have a strong background in clinical trial methodologies and oncology, combined with at least...SeniorLocal area
- ...A biotechnology company is seeking a Clinical Research Associate in Durham, NC. The ideal candidate will have 4+ years of independent monitoring experience and a solid understanding of ICH and GCP guidelines. You will work closely with investigative sites to ensure compliance...Senior
- ...Grifols is seeking a Clinical Research Associate to manage clinical monitoring processes and ensure regulatory compliance. You will track study tasks, conduct... ...investigator site interactions to support clinical trials. The ideal candidate will have a life science degree...Senior
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Senior Clinical Trial Analytics Monitor I. Be the first to apply!
- resident monitor United States
- patient monitor technician United States
- test monitor United States
- lunch monitor United States
- monitoring and evaluation specialist United States
- monitoring operator United States
- travel cardiac monitor tech United States
- computer lab monitor United States
- program monitor United States
- debris monitor United States

