ProPharma Group

Sr. Clinical Data Coordinator

ProPharma Group$80K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree or equivalent certification in allied health profession preferred
  • Minimum 3 years of data management experience required
  • Experience with Electronic Data Capture (EDC) systems required
  • Familiarity with Oracle Inform™ EDC system preferred
  • Experience in oncology or inflammatory therapeutic areas preferred

Responsibilities

  • Conduct ongoing data review and reconciliation of third-party data streams
  • Perform User Acceptance Testing (UAT) on clinical databases
  • Ensure Quality Control (QC) measures are upheld for clinical databases
  • Update Data Management-related documentation as necessary

Benefits

  • Remote work options available
  • Encouragement for hybrid office collaboration for local hires
  • Personal review of applications by recruitment team, ensuring feedback for all candidates
Full Job Description
Title: Senior Clinical Data Coordinator

FSP/Contractor

Job Summary

The Sr. Clinical Data Coordinator performs activities pertaining to the conduct of Phase I-IlI clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines to ensure that a quality work product is produced and timelines and deliverables are met.

Summary of the Essential Functions of the Job

  • Perform ongoing data review, including reconciliation of third party data streams and serious adverse event reconciliation with the safety database.
  • Perform User Acceptance Testing (UAT) of clinical databases.
  • Perform Quality Control (QC) of clinical databases.
  • Perform ongoing updates of Data Management-related documentation, as needed.


Minimum Requirements

  • 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.
  • Minimum of 3 years of data management experience is required.
  • 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.


#LI-REMOTE

#LI-AP1

All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.

Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

About ProPharma Group

ProPharma Group is a pharmaceutical consulting company that provides regulatory compliance, pharmacovigilance, and medical information services to clients in the healthcare industry. The company was founded in 2001 and is headquartered in Shawnee Mission, Kansas. ProPharma Group offers a range of services, including clinical trial support, quality assurance, and validation services. The company has worked with clients in a variety of industries, including pharmaceuticals, biotechnology, and medical devices.
Learn more about ProPharma Group
Size
500 employees
Industry
Net Income
$5 million
Founded
2001
5 Year Trend
+30%
Revenue
$50 million

Similar Jobs

More Jobs at ProPharma Group

More Pharmaceuticals & Biotech Jobs

Find similar Sr. Clinical Data Coordinator jobs: