Clinical Data Manager

IQVIA LLC

Durham (NC)

On-site

USD 69,000 - 171,000

Full time

6 days ago
Be an early applicant

Get more replies from employers

Send a job-specific resume in minutes.

Job summary

IQVIA LLC is seeking a Clinical Data Manager to oversee data management activities for Phase I-III trials in accordance with ICH/GCP. The role ensures data quality, timeliness, and budget adherence across studies.

The job includes creating and reviewing CDM documents, supporting UAT/QC activities, coordinating with data programmers, training site staff, and ensuring regulatory compliance across local and international guidelines.

Qualifications

  • Minimum 5 years of data management experience.
  • Bachelor's degree or certification in a related allied health profession is preferred.
  • Experience with Electronic Data Capture (EDC) systems is required.
  • Experience with Oracle Inform EDC system is preferred.
  • Oncology and/or inflammatory therapeutic area experience is preferred.
  • Project management experience within Data Management is preferred.
  • Work history at a CRO or CRO management experience in data management is preferred.

Responsibilities

  • Communicate key clinical data management metrics and determine actions with study team.
  • Review, develop and/or write CDM documents (CRFs, Edit Checks, DMPs, eCRF guidelines).
  • Participate in UAT and QC as needed.
  • Work with Clinical Database Programmers on Data Flow Charts and Import Guidelines.
  • Assist with site or vendor training on CDM topics.
  • Provide data review training and guidance to Senior Coordinators.

Skills

Data management
EDC systems
Oracle Inform EDC
UAT
QC
Data review
Training
Project management
CRO experience

Education

Bachelor's degree or allied health certification

Tools

Inform EDC (Oracle)

Job description

Job Summary

The Clinical Data Manager performs activities pertaining to the conduct of Phase I-III clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines. The CDM ensures, from a data management perspective, assigned trials on time, within budget, and with highest achievable quality.

Essential Functions of the Job
  • Responsible for communicating key clinical data management metrics (e.g., data entry status, query resolution and aging, etc.) and determining appropriate actions in conjunction with study team.
  • Responsible for the review, development and/or writing of clinical trial documents and manuals, including but not limited to Case Report Forms, Edit Checks, Data Management Plans, Clinical Data Review Plans and eCRF Completion Guidelines.
  • Participate in User Acceptance Testing (UAT), as needed.
  • Participate in Quality Control (QC), as needed.
  • Responsible for working with the assigned Clinical Database Programmer(s) to ensure the development of the Data Flow Chart(s), Data Transfer Specifications and Import Guidelines.
  • Assist with site and/or third party vendor training on CDM-related topics.
  • Responsible for providing data review training and guidance to Sr. Clinical Data Coordinators that are supporting their trial(s).
  • Perform data review and discrepancy resolution, as needed.
  • Responsible for archiving trial(s) and associated documentation upon trial(s) completion.
  • Ensure adherence to Good Clinical Practice and all applicable local and international regulations.
Minimum Requirements
  • Minimum of 5 years of data management experience is required.
  • Bachelor's degree OR certification in a related allied health profession from an appropriately accredited institution (i.e. RN, MT, PA, RT) is preferred, but individuals with commensurate experience will be considered.
  • Experience with Electronic Data Capture (EDC) system(s) is required.
  • Experience with Oracle Inc.'s Inform™ EDC system is preferred.
  • Oncology and/or inflammatory therapeutic area experience is preferred.
  • Project management experience (within Data Management) is preferred.
  • Work history at a Clinical Research Organization (CRO) or CRO management experience in data management is preferred.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.

https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $68,500.00 - $171,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).

Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments.

Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact.

No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Clinical Data Manager
Clinical Data Manager

IQVIA • Durham (NC)

On-site
USD 69,000 - 171,000
Manager, Clinical Operations
Manager, Clinical Operations

IQVIA • San Marcos (CA)

On-site
USD 87,000 - 216,000
Senior Global Clinical Study Manager
Senior Global Clinical Study Manager

IQVIA • Rockville (MD)

On-site
USD 100,000 - 200,000
Clinical Research Associate, Sponsor Dedicated
Clinical Research Associate, Sponsor Dedicated

IQVIA • Portland (OR)

Hybrid
USD 57,500 - 226,800
Clinical Research Associate, Sponsor Dedicated
Clinical Research Associate, Sponsor Dedicated

IQVIA • San Jose (CA)

On-site
USD 57,500 - 226,800
Competitive salary
Health benefits
Career growth opportunities
Clinical Data Manager
Clinical Data Manager

ProPharma • Raleigh (NC)

Hybrid
USD 90,000 - 120,000
Clinical Data Manager
Clinical Data Manager

PPG US ProPharma Group, LLC • Raleigh (NC)

Hybrid
USD 80,000 - 120,000
Clinical Data Manager
Clinical Data Manager

propharmagroup • United States

Hybrid
USD 90,000 - 140,000
Hybrid work model
Remote work options
Director Clinical Data Management
Director Clinical Data Management

The Steely Group • Boston (MA)

On-site
USD 100,000 - 140,000
Clinical Research Associate - Sponsor Dedicated
Clinical Research Associate - Sponsor Dedicated

IQVIA LLC • Parsippany-Troy Hills (NJ)

On-site
USD 72,000 - 189,000