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Clinical Data Manager I

Job not on LinkedIn

🕒 July 9

🌵 Arizona, Connecticut, +10 more states – Remote

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💵 $52.5k - $75k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 11%

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Logo of Perceptive Inc.

Perceptive Inc.

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Perceptive Inc. is a leading provider of scientific and data-driven solutions for the bio-pharmaceutical industry, focusing on oncology, central nervous system (CNS) therapeutic areas, and musculoskeletal imaging. With expertise in drug discovery, preclinical and early clinical imaging, and radiochemistry, Perceptive offers services that identify promising candidate compounds and mitigate risks through premier imaging services. It also provides comprehensive eClinical solutions, including Randomization and Trial Supply Management (RTSM), aimed at optimizing clinical trial processes. Trusted for its high-quality data, Perceptive serves as a partner in advancing clinical trials and bringing essential treatments to patients faster, backed by over 50 years of experience and a team of dedicated experts. Perceptive's global presence ensures seamless delivery of Discovery, eClinical, and Imaging services to support worldwide clinical trials.

📋 Description

• Deliver entire clinical trials as Clinical Data Manager • Act as sponsor-facing contact • Work with study project management and technical data management teams to meet design specifications • Monitor trial health and ensure quality and data reconciliation • Attend and participate in sponsor meetings • Manage data management deliverables for assigned studies • Understand requirements for study implementation and data collection • Collaborate with project teams to develop study-specific edit check criteria • Define, run, and review edit checks and resolve discrepant data • Maintain organized, complete, and up-to-date study documentation • Perform study setup and specifications and obtain approvals as needed • Coordinate and document receipt and processing of electronic or ancillary data from outside sources • Keep supervisor informed of project status • Review data and identify errors or inconsistencies • Collaborate with project teams to resolve data issues • Track outstanding issues and follow up until resolution • Ensure accuracy and consistency of clinical databases • Carry out CDM activities according to regulatory guidelines • Perform other duties as assigned

🎯 Requirements

• Experience and skills relevant to the role affect salary placement • Understanding requirements for study implementation and data collection • Ability to collaborate with project teams to develop study-specific edit check criteria • Ability to define, run, and review edit checks and resolve discrepant data • Ability to maintain organized, complete, and up-to-date study documentation • Ability to perform study setup and specifications and obtain approvals as needed • Ability to coordinate and document receipt and processing of electronic or ancillary data from outside sources • Ability to review data and identify errors/inconsistencies • Ability to collaborate with project teams to resolve data issues • Ability to track outstanding issues and follow up until resolution • Ability to ensure clinical data accuracy and perform CDM activities according to regulatory guidelines • Candidates located in AZ, CT, DE, FL, GA, IL, MA, MO, NH, NJ, NC, PA, UT, or VA are preferred

🏖️ Benefits

• Medical, Dental and Vision benefits for you and your family • Flexible Spending Accounts (FSA) • Health Savings Accounts (HSAs) • Paid time off policy including holidays and sick time • Internal growth and development programs & trainings • 401(k) program • Life & accident insurance • Disability insurance

Apply Now

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