Senior Clinical Data Coordinator
Senior Clinical Data Coordinator
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Job Description
The Senior Local Lab Handling Coordinator is responsible for defining and continually improving the responsibilities of the Local Lab Handling Coordinators and the process for managing local laboratory addition this senior role will act as the team leader and subject matter expert for the Local Lab Handling Coordinators.
The Senior Local Lab Handling Coordinator is also responsible for collaborating with internal and external partners to obtain the information required per the protocol to enter local laboratory information into the EDC system. This role will also be responsible for updating local laboratory information as needed throughout the progression of clinical trials in the EDC addition this role work with the relevant parties to ensure that complete and accurate analyte and reference range information is available in the EDC system for clinical trials in a timely manner.
Summary of the Essential Functions of the Job
- Defines the responsibilities of the Local Land Handling Coordinators as well as the process for managing local laboratory information
- Receives relevant local laboratory information from investigative sites and transcribes this information into the EDC system or into a template to be imported into the EDC system
- Crosschecks the information provided with the protocol to certify that all required analytes are accounted for
- Works with the Clinical Data Managers (CDMs) Clinical Research Associates (CRAs) and investigative sites to clarify any source documentation issues and obtain any further updates which might be needed
- Regular attendance at Clinical Data Management group meetings and any departmental trainings
- Serve as a mentor to team members by guiding work resolving challenges and offering support
Minimum Requirements
- Bachelors Degree or equivalent experience in clinical research or similar field
- At least 3 years of clinical or lab data review experience with experience reviewing lab/analyte data and/or lab source documentation
- 3 years experience in Data Management - start up/lock
- Third-party data recons and experience preparing DM metrics
- Experience with EDC systems (RAVE/VEEVA/INFORM/OC)
- Oncology and/or Inflammatory therapeutic area experience preferred
This role is not eligible for UK visa sponsorship
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
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. potential base pay range for this role when annualized is $49000.00 - $122300.00. 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.
Required Experience:
Senior IC
Employment Type
Full-Time
