Clinical Project Manager
Posted Updated
Job Position: Clinical Project Manager
Location: Lexington, MA
Duration: 6 Months+ (Temp to Perm)
Summary:
The Clinical Project Manager is responsible for independently managing a small number of studies of basic to moderate complexity or defined activities in more complex, multicenter studies (e.g., managing niche vendors).The Clinical Project Manager will be able to ensure study timelines and milestones are met and studies completed according to the protocol.
Manages clinical project team members to appropriate and timely completion of projects; oversees project timeline development and maintenance.
Internally interfaces with data management and biostatistics, regulatory affairs, clinical compliance, field clinical monitors, medical directors, liaison with investigators and clinical site staff.
Requirement:
Essentially they need to be able to run a clinical study Owning the time, budget, running the team meetings, making sure that the other functional groups are reporting updates, handling study sites, handling vendor oversight (these are the main components)
At least three years of Study Management (actually running the study) is needed.
Pharma experience OR working on the vendor side for clinical research organization (and have a pharma client) that is OK.
Bachelors required
Location: Lexington, MA
Duration: 6 Months+ (Temp to Perm)
Summary:
The Clinical Project Manager is responsible for independently managing a small number of studies of basic to moderate complexity or defined activities in more complex, multicenter studies (e.g., managing niche vendors).The Clinical Project Manager will be able to ensure study timelines and milestones are met and studies completed according to the protocol.
Manages clinical project team members to appropriate and timely completion of projects; oversees project timeline development and maintenance.
Internally interfaces with data management and biostatistics, regulatory affairs, clinical compliance, field clinical monitors, medical directors, liaison with investigators and clinical site staff.
Requirement:
Essentially they need to be able to run a clinical study Owning the time, budget, running the team meetings, making sure that the other functional groups are reporting updates, handling study sites, handling vendor oversight (these are the main components)
At least three years of Study Management (actually running the study) is needed.
Pharma experience OR working on the vendor side for clinical research organization (and have a pharma client) that is OK.
Bachelors required
Regards
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Pooja Mishra | Team Recruitment | Mindlance, Inc. | Office: 732-243-0715