CLINICAL RESEARCH ASSOCIATE (CRA II/SENIOR) - SOUTHEAST - PAREXEL
Company: PAREXEL
Location: Rosemead
Posted on: September 17, 2024
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Job Description:
Working with heartAt 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.A
little about usParexel is proud to be a leading Clinical Research
Organization with team members across the globe. As a member of our
team, you will get to know your colleagues on a personal level.
Have a question? A clinical research leader, project team member,
technology "super user" or colleague are a phone call away. Our
clinical research teams meet regularly to have discussions in an
open environment, allowing our team members to share their
expertise and promote learning within the team. Management supports
and encourages career growth through consistent performance
discussions and evaluations. Whether your interest is to progress
into a more senior level CRA role, into line management, Quality,
Project Leadership or a variety of other positions, Parexel prides
itself on career opportunities for our employees.More about youOn
your first day we'll expect you to have:18+ months Clinical
Research Associate (CRA) monitoring experience in clinical research
with understanding of clinical trials methodology and
terminology.Bachelors or equivalent degree in biological science,
pharmacy or other health related discipline.Strong interpersonal,
written, and verbal communication skills within a matrixed
team.Ability to work in a self-driven capacity with a sense of
urgency and limited need for oversight.A client focused approach to
work with a flexible attitude with respect to assignments and new
learning.The ability to manage multiple tasks, evaluate a variety
of unpredictable scenarios and achieve project timelines while
being able to apply your understanding of study protocol(s).An
honest and ethical work approach to promote the development of life
changing treatments for patients.Strong computer skills, including
but not limited to the knowledge of a Clinical Trial Management
System (CTMS), Electronic Document Management System (EDMS) and
MS-Office products such as Excel and Word.#LI-REMOTE
Keywords: PAREXEL, Inglewood , CLINICAL RESEARCH ASSOCIATE (CRA II/SENIOR) - SOUTHEAST - PAREXEL, Healthcare , Rosemead, California
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