# Clinical Trial Coordinator - Drug Reconciliation

**Company**: Fortrea
**Location**: Durham
**Job type**: full-time
**Salary**: $55-65K
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Durham/FSP---Clinical-Trial-Coordinator---Drug-Reconciliation_266704?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/clinical-trial-coordinator-drug-reconciliation-fa8f2e81-0ac/

## Description

Fortrea is seeking a Clinical Trial Coordinator - Drug Reconciliation to provide day-to-day support for drug reconciliation in clinical trials.

The successful candidate will serve as a point of contact for Clinical Operations teams on clinical drug supply reconciliation issues, create and manage Excel trackers for drug reconciliation, review documentation, collaborate with internal teams, and communicate with Clinical Research Associates (CRAs).

Key responsibilities include:

- Providing support for drug reconciliation in blinded and unblinded studies

- Serving as a point of contact for Clinical Operations teams on drug supply reconciliation issues

- Creating and managing Excel trackers for drug reconciliation at each site

- Reviewing documentation for drug reconciliation, such as clinical supply return forms and drug accountability logs

- Collaborating with internal Clinical Operations teams and updating Clinical Research Managers

- Communicating with blinded and unblinded CRAs to manage the drug reconciliation process

- Identifying risks and assisting with corrective action plans

- Assisting in reviewing IRT/IVRS shipping history to manage drug reconciliation

- Providing logistics support and oversight of clinical supply when IRT/IVRS systems are not available

- Maintaining supply inventory tracking records and providing training to CRAs

- Creating databases in SharePoint for CRAs to enter documentation

- Reviewing and uploading clinical supply return forms and conducting quality checks

- Maintaining yearly checks in eTMF for drug reconciliation documents

- Conducting weekly and monthly calls with Clinical Research Managers to provide updates and support

- Providing quality checks to CTMS and Veeva vault documentation

- Creating country memos after drug reconciliation is finalised

The ideal candidate will have:

- A university or college degree in life sciences or a related field, or certification in a related allied health profession

- 0-2+ years of experience in a related field, or an equivalent combination of education and experience

- Working knowledge of ICH, RA, IRB/IEC, and other applicable regulations/guidelines

- Basic understanding of the clinical trial process

The role requires proficiency in Excel, and familiarity with IRT and IVRS systems is desirable.

The target pay range for this hourly role is $55-65K.

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## Skills

### Required
- Excel
- ICH
- RA
- IRB/IEC
- clinical trial process

### Nice to have
- IRT
- IVRS

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Source: [Apply at fortrea.wd1.myworkdayjobs.com](https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Durham/FSP---Clinical-Trial-Coordinator---Drug-Reconciliation_266704?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)