Clinical Operations Manager
About the role
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Are you passionate about
improving the quality of human life? If so, we invite you to learn more about
our home-based CRA Manager opportunities.
ICON Clinical Research has a strong reputation in our approaches to clinical
development. We apply scientific and operational excellence across all phases
of clinical trial outsourcing services for our clients. We work with top
pharmaceutical organizations on emerging therapeutic areas which include but
are not limited to Oncology, Vaccines, CNS, Cardiovascular and Pain.
We are presently in over 40 countries with over 80 offices worldwide and over
11K employees globally. We are comprised of 6 divisions and offer a
full-service portfolio of solutions to our clients.
Overview of the Role
We support our line CRA Managers to effectively manage our CRAs to ensure
high performance, quality of monitoring and continue development. We offer a
strong benefits package that includes a comprehensive health plan, retirement
plans, competitive pay, performance bonus and vacation. Additionally, we have
cutting edge technology to ensure better outcomes.
Our CRA Managers will ensure CRAs perform monitoring and site management
responsibilities to an appropriate working standard including (but not limited
to ):
- updating study files
- completing trip reports and follow-up letters in a timely manner
- managing investigational product
- completing source data verification
- developing effective relationships with sites
Monitor and evaluate CRA workloads and liaise with Resource Management, the
relevant Project Manager and Director of Clinical Operations (as needed) to
ensure appropriate allocation of resources and optimal utilization and
workload. Accompany CRAs to provide on-site training for pre-study,
initiation, monitoring and close-out sites. Conduct on-site Monitor
Assessment Visits as required. Implement individual development and provide
coaching and mentoring to assigned CRAs.
Prior experience of
managing CRAs.
Fundamental knowledge of Clinical Research, and expertise in all phases of
clinical trail.
Comprehensive knowledge and understanding of ICH-GCP.
Previous experience in delivering training.
Ability to liaise successfully with clinical project teams and other relevant
departments.
Requirements
Bachelors’ Degree or local equivalent in, life sciences, medicine or related
discipline
Minimum of six ( 6) years of clinical research experience with at least four
(4) years of relevant experience as a Senior CRA or Principal CRA (in a Lead
CRA role) or at
least two ( 2) years as a Project Manager CRA Manager or equivalent job role.
We invite you to review our clinical opportunities at www.iconplc.com/careers.
We provide equal opportunity to all qualified applicants and employees by prohibiting discrimination in employment decisions because of race, color, religion, sex, national origin, age, veteran status or disability.
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
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