Everest Clinical Research Services Inc. is expanding at an phenomenal rate and as such we need to add several Project Managers to our team. If you want to join an organization with exceptional opportunities and career growth then please read on. Now is the time for you to join an exceptional and winning team!
Everest Clinical Research Services Inc. ("Everest") is a contract research organization providing statistical, data management, clinical trial monitoring and medical writing services to pharmaceutical and biotechnology companies. We serve some of the best-known companies worldwide, and work with many of the most advanced drugs in development today. Our Corporate Headquarters is in Markham (Greater Toronto Area), Ontario, Canada with U.S. operations in Little Falls (Greater New York City Area), New Jersey, USA. As we continue to expand our business, we are currently seeking highly qualified and motivated individuals to work in either our Markham, Ontario or our Little Falls, New Jersey offices as PROJECT MANAGERS.
PROJECT MANAGER, CLINICAL RESEARCH AND DEVELOPMENT
This position is responsible for defining project scopes, planning, directing, controlling project activities, managing resources and project team performance of cross-functional teams engaged in clinical research and development activities. This position is also accountable for reporting of project progress status to Everest internal management and its clients. These activities include but not limited to managing projects with activities focused on data management, statistics, medical writing, drug supply management, administration of data monitoring and adjudication committees, as well as preparing drug submissions to regulatory agencies. When required, the incumbent may perform clinical trial planning, management, and site monitoring from the initiation of a trial to its closure.
Qualifications and Experience:
A Bachelor or Master of Science degree in life science or health related field, with a minimum of 5 years of experience in clinical research and development within a pharmaceutical , biotechnology or CRO setting.
Demonstrated understanding of cross-functional processes including clinical operations, statistics, data management, drug supply management, regulatory affairs, and medical writing.
Knowledge and understanding of ICH guidelines, FDA, Health Canada, and EMA regulations.
Ability to define scope, plan and manage projects, including resource requirements and utilization, budgets, key deliverables and timelines.
Demonstrated leadership abilities, including setting goals for others and driving to achieve them in accordance with allocated resources, timelines, and budgets.
Excellent interpersonal, oral and written communication skills. Demonstrated strong negotiation and presentation skills
Strong ability in problem-solving including conflict resolution.
Experienced as a clinical trial monitor, initiating, monitoring and closing out clinical trials will be desirable.
Fluency in French, including medical and scientific terminology, will be an asset.
How to Apply:
Please send your application, indicating the position to which you are applying.
We are an equal opportunity employer. We thank all interested applicants, however, only those selected for an interview will be contacted.
To find out more about Everest Clinical Research Services Inc. and to review other opportunities please visit our WEB site at www.ecrscorp.com.