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.
Clinical Research Associate (CRA II/Senior) - West (Oncology)
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. Your hard work may be rewarded through a bonus incentive program, the opportu...
Senior Clinical Research Associate - Oncology - West Coast
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
Clinical Research Associate (CRA II/Senior) - West
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. Your hard work may be rewarded through a bonus incentive program, the opportu...
Senior Clinical Research Associate - West Coast
The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical study activities, departmental tasks, and provides mentoring to other CRA team members within established protocols and portfolio under general supervision. Works with Clinical Trial Oversight Managers (CTOM...
Senior Project Manager / Associate Director, Project Management - Metabolic Disease (Obesity/T2 Diabetes) - US or Canada - Remote Based
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Senior Project Manager / Global Project Lead. ...
Real Estate Project Manager
Commercial Real Estate Project Manager. Spearhead initial project analysis, market research, and development feasibility studies. Manage construction projects, ensuring adherence to budget, schedule, and quality standards. Maintain rigorous financial oversight on project expenditures and justificati...
Service Delivery Project Manager, Colocation
They are seeking a Service Delivery Project Manager to join their team. The Service Delivery Project Manager will be responsible for managing the end-to-end delivery of colocation and cloud services. This includes overseeing project management processes to ensure timely and accurate implementation o...
Construction Project Manager - Western Region
Customer Service - developing and maintaining relationships with Dutch Bros construction partners during all phases of construction 3) Organization and Management of Projects: review and analyze project drawings and documents, manage costs and profitability, coordinate and manage multiple tasks to e...
SAP S/4 Project Manager (REMOTE)
The Project Manager works closely with senior management to make sure that the scope and direction of each project is on schedule, as well as coordinates with other departments for support. The Project Manager will need to focus on both Business and MIS resources, processes, and deliverables. Follow...
Reconstruction Project Manager
We are seeking a Reconstruction Project Manager to join our team! You will oversee project planning, scheduling, budgeting, and implementation. Oversee all aspects of construction project from planning to implementation. Allocate resources for assigned projects. Interface with project inspectors, co...