Clinical Research Associate (CRA) - West (Remote)
Company: PAREXEL
Location: Mount Dora
Posted on: August 6, 2022
|
|
Job Description:
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---re set up for success. As the
clinical sites--- sole point of contact, this includes addressing
and resolving site issues and questions. You---ll 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
could 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 the completeness and quality of Regulatory
Documentation and perform site document verification.
Qualifications More about you On your first day we---ll expect you
to have: Site Management or equivalent experience in clinical
research, with understanding of clinical trials methodology and
terminology. Ability to perform all clinical monitoring activities
independently. Bachelor---s or equivalent degree in biological
science, pharmacy or other health related discipline. Strong
interpersonal, written, and verbal communication skills within a
matrixed team. Experience working in a self-driven capacity, with a
sense of urgency and limited oversight. A client-focused approach
to work and flexible attitude with respect to assignments/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. A little about us
Parexel is proud to be a leading Clinical Research Organization
with colleagues across the globe. As a member of our team, you---ll
get to know your coworkers on a personal level. Have a question? A
clinical research leader, project team member, technology ---super
user--- or collaborator 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. This role may be subject
to government and/or customer requirements regarding vaccination
against COVID-19 that are more stringent than Parexel policy.
Accordingly, successful applicants may need to be either vaccinated
against COVID-19 or have an approved religious or medical
exemption. Employment is contingent on disclosure of your COVID-19
vaccination status and, if relevant, proof of vaccination. EEO
Disclaimer Parexel is an equal opportunity employer. Qualified
applicants will receive consideration for employment without regard
to legally protected status, which in the US includes race, color,
religion, sex, sexual orientation, gender identity, national
origin, disability or protected veteran status. LI-REMOTE
Keywords: PAREXEL, Orlando , Clinical Research Associate (CRA) - West (Remote), Healthcare , Mount Dora, Florida
Click
here to apply!
|