When our values align, there's no limit to what we can achieve.
Working with heart
At the end of the day we’re all patients. Because of this, the Parexel team takes our work personally and does it with empathy and heart.
When our values align, there’s no limit to what we can achieve. Our clinical operating model drives effectiveness, reduces handoffs and increases employee, client and site satisfaction.
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge.
We hire talent that takes initiative to do things better, smarter and faster- people who want to grow personally and professionally.
Your time here
At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success.
As the clinical sites’ sole point of contact, this includes addressing and resolving site issues and questions. You will also manage site quality and delivery from site identification through to close-out.
As a CRA, Parexel will offer you world class technology and training catered to your individual experience. You can anticipate less travel and a lower protocol load in comparison to industry peers.
Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research.
If impact, flexibility, and career development appeal to you, Parexel may be your next home.
What you’ll do
- Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit / contact reports.
- Build relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.
- Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol.
- Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines while also Ensuring compliance with the approved standard operating procedures (SOPs), protocol / amendment(s), GCP, and the applicable regulatory requirement(s).
- Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability.
- Execute. Monitor completeness and quality of Regulatory Documentation and perform site document verification.
Senior Wealth Associate
A career as a Senior Wealth Associate at National Bank is a job where you can showcase your ability to work in synergy with clients and colleagues. National Bank Financial – Wealth Management is the fifth largest investment dealer in Canada. ...
Clinical Research Associate II
Clinical Research Associate II. To qualify for this role, you must have minimum 2 years experience working in conducting clinical studies. Responsible for execution of general tasks and monitoring tasks of clinical studies. Participates in the creation of clinical documents which may include protoco...
Equity Research Associate - Real Estate
Are you interested in joining a diverse and collaborative environment where you will have the opportunity to learn continuously and develop professionally? Are you excited by the opportunity to develop relationships with research professionals, institutional investors and other capital markets indiv...
(Senior) Reimbursement & Health Outcomes Research Associate
Critically appraise and interpret health outcomes research studies (e. Support the Patient Access team with administrative processes related to research projects (e. Understanding of Health Economics, Health Technology Assessment, and the reimbursement landscape in Canada. ...
Senior Clinical Trial IWRS Monitor
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. To drive continued success in this exciting clinical research ...
Clinical Research Coordinator II, Orthopedic Surgery
Write grant applications, literature reviews, manuscript writing, presentation of research findings and coordination of multicenter research clinical trials (RCT’s). Sinai Health is looking for a Clinical Research Coordinator to support our Division of Orthopaedic Surgery at Mount Sinai Hospital. Th...
Senior Business Analyst (Research and Development)
Leads and contributes to the planning, design and execution of R&D initiatives, including defining and elaborating research proposals and relevant requirements, designing the research methodology, preparing the data and environments, developing proof of concepts, and documenting and communicating re...
Canada Research Chair (Tier 1) in Technology, Society and Disability (Associate/Full Professor)
This CRC will develop and expand their research in this area and seek interdisciplinary collaborations within the Faculty and across the University, including through participation in its associated Research Centres (Centre for Integrative and Applied Neuroscience (CIAN), (CAIS), (ITS) and many ) an...
Senior Actuarial Production Associate
Senior Actuarial Production Associate. Senior Actuarial Production Associate. Equitable is growing! We are looking for a self-motivated Senior Actuarial Production Associate to join our Individual Actuarial Production team! Our new team member should have excellent analytical skills, a keen attentio...
Clinical Research Safety Associate
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. Clinical Research Safety Associate . Support medical writing a...