Esds Assistant

JOB DESCRPITION

The employee will be delivering support to the Early Stage Development Europe Operational team. He/she will be providing operational support and project support (responsible for in-house activities as well as for compliance with processes required to initiate, maintain, support and close out the early stage clinical trials managed by the department) and will carry out tasks for the support of clinical grants.

For this hybrid role, the tasks will include but are not limited to:
ESDS assistant tasks:

- Assemble and provide support for timely Clinical Trial Submissions and availability of

Essential Documents for clinical trials.
- Create Essential Documents Repository.
- Assemble and track availability of all essential documentation required for study conduct.
- Provide professional presentation of study materials for investigator/vendor or country operations meetings
- Liaise with sites and in house departments to ensure appropriate regulatory follow-up
- Organization and documentation (minutes) of project team meetings where need be
- Operational and project support activities, including, but not limited to:

- Update, maintain and monitor CTMS to allow accurate project management, regulatory reporting and clinical grants payments
- Follow-up/check final accountability of IMP and return or destruction as appropriate
- Possibility for SME roles: CTMS, TMF steward, SIP, CLMS, Safety reporting tracking

Support of clinical grants tasks:

- Review study budgets/clinical trial agreements for consistency with study protocol
- Updating of clinical and study planning databases

Review study budgets/clinical trial agreements for consistency with study protocol
- ABC (anti-bribery + corruption checks) on all HCP (fact finding, workflows, tracking, renewals) + troubleshooting with compliance, technical services etc.
- Clinical trial payments and payment tracking
- Financial disclosure (check need, track, process letters and documentation)
- Denied parties screening (DPS)
- Compliance checks
- Disclosure agreements: Generate and track Trial master file reconciliation of clinical grants/compliance documents
- Maintenance of trackers
- GMS (grants management system): enter and track payments, run reports execute payments in COMET (SAP), purchase orders as needed

**Requirements**:
Bachelor degree (e.g. medical assistant, or paramedical education) or relevant work experience in clinical research field
- Advanced communication skills (written and verbal) in local languages and English
- Understanding and knowledge of study protocols and study working documents, lab manuals, etc
- Good understanding of the clinical research processes
- Understanding of the ICH/GCP (international good clinical practice guidelines and harmonization) and local clinical trial regulations

**Search Firm Representatives Please Read Carefully**

**Employee Status**:
Regular

**Relocation**:
No relocation

**VISA Sponsorship**:
**Travel Requirements**:
**Flexible Work Arrangements**:
**Shift**:
**Valid Driving License**:
**Hazardous Material(s)**:
**Number of Openings**:
1
**Requisition ID**:R211991