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Open nowPosted 3916 days ago

Clinical Project Manager

Integrated Resources INC2,463 open roles

Where
Lexington, MA, United States
Work mode
On site
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Your applicationOpen nowClinical Project ManagerIntegrated Resources INC · Lexington, MA, United States

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The clock on this job

Early applications get read.

12.1% of postings close within 7 days. Measured by our own scanner across the market. Integrated Resources INC postings stay open a median of 15 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.1%7 days
  4. 19.1%14 days
  5. 35.6%30 days
  6. 52.7%60 days
This job: posted 3916 days ago

Integrated Resources INC median: 15 days open

The posting

Company Description

At 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 Description

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.

Qualifications

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

Additional Information

Regards ___________________________________________________________________________________________________ Pooja Mishra | Team Recruitment | Mindlance, Inc. | Office: 732-243-0715

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