CRA II
TA Business Partner
- Full Service Division
About the role
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Clinical Research Associates have a career that
enables you to contribute directly to the development of new therapies that
impact millions of lives around the globe. We are looking for an experienced monitor to join our team. We seek people who are passionate about improving the quality of human
life through scientific research. Our
CRAs partner with investigative sites to ensure applicable guidelines for human
safety and ethics are being followed, data is accurate, and study procedures
are being followed.
We are a multi-national top five clinical
research organization. You will join a team
of strong professionals and a management team dedicated to your career
development. Some of our best people
grew into key leaders in the company. We
are a company of 13,500 employees in forty countries globally. We
differentiate ourselves by developing innovative solutions to bring life-saving
drugs to market faster and in a more cost-effective way to foster better
patient outcomes. We are a top five
clinical research organization with solid earnings and growth potential. Our belief in excellence is our core value in
all that we do for our sponsor partners and the patients that we serve.
As a company we strive to exceed our customers’ expectations in drug
development solutions.
We
care about our people, since they are the key to our success. We provide an
open and friendly work environment where we empower people and provide them
with opportunities to develop their long term careers. Caring for
patients while enjoying what we do and delivering great results is something we
can achieve if we know we can count on each other and have a clear vision of
where we want to go.
Foremost, you will also be an expert in the study
protocol to ensure it is being adhered to, that data is clean and accurate, and
that trial participants are consenting and being treated in an ethical
manner. You will carefully review
medical records; visually inspect storage and handling of investigative
products and supplies; communicate questions, concerns, and discuss findings
with the clinical staff and investigators; identify obstacles and solutions for
overcoming them; and discuss corrective actions when issues arise. You will at all times stay in close contact
with your sites about their progress.
Additionally you will ensure that all regulatory filings are
current. You’ll ensure that the trial is
operating according to guidelines like ICH/GCP, that it is complying with laws
and regulations, and that standard operating procedures are being
followed.
We’re seeking CRAs who see their role as beyond
mere fact checking. We are looking for monitors who can spot
trends and underlying concerns for the best possible outcomes. Our CRAs don’t sit on the sidelines. They are active participants in the well-being
and management of their clinical sites. We
are looking for people who enjoy that no two days will be alike.
We look for people with experience in site
monitoring who can read and interpret medical records, review findings, and who
have a deep understanding of local and international laws and guidelines for
the conduct of clinical trials.
We invite you apply to our clinical research
associate opportunities for Phases II - IV. We are seeking experienced CRAs with a desire
to travel. A bachelor’s degree in the
life sciences preferably will ensure your familiarity with regulatory
guidelines and clinical terminology. A
minimum two years of site monitoring experience will ensure your success on our
team. The
ability to speak fluently and write in English is required.
Application process
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Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.
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