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 Clinical Research Associate - CNS - Central Region
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. Anchored in our company’s scientific heritage, o...
Senior Principal Research Scientist I or II - Drug Product Development
We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. Collaborates with experts within function to integrate scientific objectives into activiti...
Clinical Research Associate II
Position Details Posting Category Research - Non Academic Working Title Clinical Research Associate II Job Title Clincal Research Associate L2 Salary Grade RA15S Appointment Type B1 - REG MGR PROF SALARY Salary Range $42,000 - $63,000/annual Job Requisition Begin Date 05/22/2024 Application Review D...
Senior Clinical Research Associate - CNS - Midwest
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. Anchored in our company’s scientific heritage, o...
Clinical Research Associate I
Position Details Posting Category Research - Non Academic Working Title Clinical Research Associate I Job Title Clinical Research Associate L1 Salary Grade RA14H Appointment Type C2 - REG OFF/SERV HRLY Salary Range - Job Requisition Begin Date 01/10/2024 Application Review Date 10/01/2024 Review Dat...
Senior Project Manager / Associate Director, Project Management - Metabolic Disease (Obesity/T2 Diabetes/CV) - 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. Associate Director, Project Management. Senior P...
Postdoctoral Research Associate/Hematology/Oncology
Postdoctoral Research Associate Advertisement – The Division of Hematology & Oncology, University of Nebraska Medical Center (Omaha), seeks a postdoctoral research associate to join Dr. This position conducts translational research in a pancreas cancer laboratory and collaborates with faculty in ong...
Senior CRA - CNS - Central Region
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. Anchored in our company’s scientific heritage, o...
Postdoctoral Research Associate | University of Nebraska Medical Center
The post-doc scholar will receive mentorship, and the research projects are expected to generate high-impact publications and provide a post-doctoral fellow with an excellent opportunity for further career development in academia as an independent investigator. ...
IT Project Manager
IT Project Manager oversees IT integration and new office start-up projects,. Manage IT integration projects for new and existing acquisitions, to include procurement for on-premises IT systems, practice management/EHR systems, email/communications, ISPs, and telephon. Training and onboarding for IT...