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Clinical Project Manager

Integrated Resources, Inc

Lexington, Massachusetts

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JOB DETAILS
JOB TYPE
Contractor
SKILLS
Biostatistics, Biotech and Pharmaceutical, Budgeting, Clinical Monitoring, Clinical Practices/Protocols, Clinical Research, Clinical Trial, Clinical Trial Management, Data Management, Project Development, Project Tracking, Project/Program Management, Regulations, Team Lead/Manager, Technical Leadership, Time Management, Vendor/Supplier Management
LOCATION
Lexington, Massachusetts
POSTED
3 days ago
Clinical Project ManagerAt Mindlance, we strive to deliver value through the combination of right people, processes, technologies and program management solutions. Our methods include applying domain expertise in specific industry segments, utilizing a highly-skilled workforce, leveraging a proven global delivery model, implementing structured and scalable quality processes and methodologies and yet, staying cost-effective. All in all, our expertise lies in providing trained and committed minds to help meet your business objectives, irrespective of the stage your business is in.Job DescriptionJob 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.QualificationsRequirement: 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.

About the Company

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Integrated Resources, Inc