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) - Central (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...
Clinical Research Coordinator II, Oncology
Knowledge of Federal and State regulations and International Guidelines related to Good Clinical Practices in clinical research. Maintains clinical and/or research databases for identified programs/ specialty clinics. Collects data used for multiple purposes, which may include process improvement ac...
Clinical Research Associate (CRA II/Senior) - Northeast (Ophthalmology)
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...
Division Chief - Hematology And Medical Oncology/associate Director - Translational & Clinical Research
Posting Summary Functional Position Title DIVISION CHIEF - HEMATOLOGY AND MEDICAL ONCOLOGY/ASSOCIATE DIRECTOR - TRANSLATIONAL & CLINICAL RESEARCH Position Number Appointment Type Regular Location-City New Orleans School/Division MEDICAL SCHOOL Department Med-Hematology and oncology Position Summary ...
Clinical Research Associate (CRA II/Senior) - Northeast (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...
Associate Clinical Research Coordinator - Baptist
The Associate Clinical Research Coordinator functions as project manager for clinical trials in assigned area(s) of responsibility. Maintains competency in requirements and regulations associated with the conduct of clinical trials and other related research activity. Organizes and manages all docum...
Clinical Research Coordinator I, II & III (Covington, LA)
Certification as a Certified Clinical Research Coordinator (CCRC through the Association of Clinical Research Professionals or ACRP) OR Certified Clinical Research Professional (CCRP through the Society of Clinical Research Associates or SoCRA)• Supervisory experience Compensation Information This p...
SAP SuccessFactors Data Migration Lead & Employee Central, Senior Associate
As a Senior Associate, you'll work as part of a team of problem solvers, helping to solve complex business issues from strategy to execution. Certification in SAP SuccessFactors Employee Central. Leading full life-cycle implementations of SAP SuccessFactors Employee Central from planning to configur...
Associate Clinical Research Coordinator
Coordinates and oversees patient (study participant) activity as it relates to the conduct of research and clinical trials including informed consent under direction and supervision of more senior research staff. Knowledge of the requirements and regulations associated with the conduct of clinical t...
Clinical Research Coordinator - Oncology
Working knowledge of the requirements and regulations associated with the conduct of clinical trials and other related research activity. Required - 3 years of relevant research experience in a clinical setting,. Knowledge of medical and clinical research terminology and processes. Coordinates and o...