JOB DESCRIPTION
Join us in our
exciting journey!!
As an experienced Clinical Research Associate,
you could be looking to broaden your therapeutic, geographic or study exposure.
Or perhaps you are looking a future beyond monitoring with our selection of
development opportunities. At IQVIA, you’ll have training and development to
plan and progress your career in the direction you choose; we do not believe in
a ‘career ceiling.’
This role is working in ourcore clinical site
management function. The team works with multiple sponsors across a multitude
of therapy areas and phases giving you the opportunity to improve and develop
your experience. With strategic site relationship managers supporting you
throughout your role this is a fantastic opportunity for you to embed yourself
in the wider clinical operations team and work on ground-breaking new medicine
development.
Responsibilities
Perform site selection
(if applicable), initiation, monitoring and close-out visits in accordance with
contracted scope of work and good clinical practice.
If applicable, may be
accountable for supporting development of project subject recruitment plan on a
per site basis. Work with sites to adapt, drive and track subject recruitment
plan in line with project needs to enhance predictability.
Provide monitoring
visits and site management for a variety of protocols, sites and therapeutic
areas.
Administer protocol
and related study training to assigned sites and establish regular lines of
communication with sites to manage ongoing project expectations and issues.
Evaluate the quality
and integrity of study site practices related to the proper conduct of the
protocol and adherence to applicable regulations. Escalate quality issues as
appropriate.
Manage the progress of
assigned studies by tracking regulatory submissions and approvals, recruitment
and enrollment, case report form (CRF) completion and submission, and data
query generation and resolution. May support start-up phase.
Create and maintain
appropriate documentation regarding site management, monitoring visit findings
and action plans by submitting regular visit reports, generating follow-up
letters and other required study documentation.
Build awareness of
features and opportunities of study to site.
Collaborate and liaise
with study team members for project execution support as appropriate.
Required Knowledge,
Skills And Abilities
Basic knowledge of,
and skill in applying, applicable clinical research regulatory requirements;
i.e.,
Good Clinical Practice
(GCP) and International Conference on Harmonization (ICH) guidelines
Good therapeutic and
protocol knowledge as provided in company training
Computer skills
including proficiency in use of Microsoft Word, Excel and PowerPoint and use of
a laptop computer
Good written and
verbal communication skills including
Good organizational
and problem-solving skills
Effective time
management skills
Ability to establish
and maintain effective working relationships with coworkers, managers and
clients
Minimum Required
Education And Experience
Bachelor's degree in a
health care or other scientific discipline or educational equivalent,
At least 2 years of
CRA experience of on-site monitoring visits,
Requires frequent
travel to sites
Excellent command of
Arabic and English language
WHAT WE OFFER:
We offer genuine
career development opportunities for those who want to grow as part of the
organization
The chance to work on
cutting edge medicines right at the forefront of new medicines development
IQVIA has access
to significant data pools allowing better site selection and recruitment. This
helps drive performance of sites making the CRA role more efficient and
discussions at site more productive. Next generation clinical development!
Flexible conditions
and an attractive remuneration package
WE INVITE YOU TO JOIN IQVIA™
Recognized byGreat
Place to Workas the second best company to work for in Spain (March 2019)
FORTUNE Magazine's
World's Most Admired Companieslist for the third year in a row.
Recognized by the 2016
Scrip Awards as theBest Full-service Provider Contract Research Organization(CRO)
Awarded the 2016 Eagle
Award from the Society for Clinical Research Sites (SCRS) for the fourth
consecutive year.
A site-nominated award
recognizing contract research organizations (CRO) and biopharmaceutical sponsors
dedicated tobuilding positive relationships with research sites through
leadership, professionalism and integrity.
IQVIA™ named in The
International Association of Outsourcing Professionals (IAOP) 2017 Global
Outsourcing 100® List which recognizes the world’s best service providers
across a range of industries.
IQVIA™ is anequal opportunity employer. We
make employment decisions based on qualifications and merit. We prohibit
discrimination based on any unlawful consideration such as age, race, national
origin, gender or other "protected status.“
We know that meaningful results require not
only the right approach but also the right people. Regardless of your role,we
invite you to reimagine healthcare with us. You will have the opportunity to
play an important part in helping our clients drive healthcare forward and
whatever your career goals, we are here to ensure you get there!
At IQVIA, we believe in pushing the boundaries
of human science and data science to make the biggest impact possible – to help
our customers create a healthier world. The advanced analytics, technology
solutions and contract research services we provide to the life sciences
industry are made possible by our 70,000+ employees around the world who apply
their insight, curiosity and intellectual courage every step of the way.
https://jobs.iqvia.com/job/-/-/24443/18233761376?source=LinkedIn_Slots
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