Person2Person, LLC
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| Clinical Study Manager Based in Northern, NJ |
| Outstanding Contract opportunity with a global pharmaceutical Company focused on multiple therapeutic areas including Neurology, Oncology and Critical Care. They continue to move forward with an entry into biologics with the development of therapeutic antibodies and other such agents, which contributes to their innovate drug discovery process. Be a part of this global market leader! |
| SCOPE & DUTIES |
The Study Manager will be accountable for the overall management of all clinical studies.
• Collaborates with other functional teams to coordinate the development and finalization of key
study documents including protocols, case report forms, informed consent documents, study
management plans and final clinical study reports.
• Responsible for monitoring studies against defined milestones and timelines to assure that all
deliverables are met.Expected to facilitate the development and implementation of remedial activites
when necessary.
• Must be willing to assume monitoring, co-monitoring responsibilities as needed.
• As a member of the Clinical Operations Team responsible for executing operational activities in
accordance with SOPs. Must enjoy working in a fast paced, matrix team environment.
• Collaborates with other functional teams to coordinate the development and finalization of key
study documents including protocols, case report forms, informed consent documents, study
management plans and final clinical study reports.
• Responsible for monitoring studies against defined milestones and timelines to assure that all
deliverables are met.Expected to facilitate the development and implementation of remedial activites
when necessary.
• Must be willing to assume monitoring, co-monitoring responsibilities as needed.
• As a member of the Clinical Operations Team responsible for executing operational activities in
accordance with SOPs. Must enjoy working in a fast paced, matrix team environment.
| REQUIREMENTS |
BS Degree or higher with a minimum of 5 years of Study Management required. Oncology experience
preferred, must have majored in Chemistry, Biology or in a scientific field, Advanced degree desired
(Masters/ Nursing Preferred). Big Pharma experience and Longevity in work history preferred.
Experience with eCRFs and InForm database required. Must have the interpersonal skills needed to
communicate successfully with the Principle Investigators, Study Coordinator, and CROs.
40 hour work week - 5 days on-site
preferred, must have majored in Chemistry, Biology or in a scientific field, Advanced degree desired
(Masters/ Nursing Preferred). Big Pharma experience and Longevity in work history preferred.
Experience with eCRFs and InForm database required. Must have the interpersonal skills needed to
communicate successfully with the Principle Investigators, Study Coordinator, and CROs.
40 hour work week - 5 days on-site
| Executive Recruiting Specialists in the NY/NJ/CT Region |
Apply today! For immediate consideration, please email resume to: lsydor@person2personllc.com |