ENGLISH SPEAKING ACTIVITY ASSISTANT

JR France; Niort; Sur place; EUR 50 000 - 70 000; Plein temps

Résumé du poste

A leading company is seeking a dedicated Pharmacovigilance Specialist in Niort to oversee compliance with regulatory standards. The role involves training junior team members, managing client projects, and ensuring quality control in pharmacovigilance activities. Candidates should have a Pharmacy degree and extensive experience in the field, along with proficiency in Microsoft Office and PV databases. Fluency in English and French is required.

Qualifications

• Minimum 5-10 years experience working for service providers.
• Previous experience in data entry, management, or pharmacovigilance (preferably 5+ years).

Responsabilités

• Key trainer for junior team members to increase quality and expand knowledge of PV case processing.
• Manage larger client projects and act as single point of contact for the client.
• Perform Quality Control/Medical Review and provide support to the team.

Connaissances

Team Management

Organization skills

Team Spirit

Methodical

Communicant

Ability to make decisions

Rigour

Adaptability

Microsoft Office

Fluent in both English and French

Formation

Pharmacy graduate

Outils

Microsoft Office

PV databases

Description du poste

Social network you want to login/join with:

ENGLISH SPEAKING ACTIVITY ASSISTANT, Niort

col-narrow-left

Client:

ProductLife Group

Location:

Niort, France

Job Category:

Other

Virtual job fairs

EU work permit required:

Yes

col-narrow-right

Job Reference:

2673119118827192320327645

Job Views:

1

Posted:

16.05.2025

col-wide

Job Description:

PLG is looking for a dedicated Pharmacovigilance Specialist - Case Processing to join our hub to oversee and work closely with our PV team to ensure compliance with regulatory standards and accurate safety data.

Responsibilities:

1. Key trainer for junior team members to increase quality and expand knowledge of PV case processing.
2. Review and identify areas of improvement.
3. Provide expertise and act as SME for the team, ensuring understanding of tasks by case management team.
4. Manage larger client projects and act as single point of contact for the client.
5. Monitor client KPIs.
6. Support in the resolution of NC/CAPA, identify RCA and implement improvements.
7. Perform Quality Control/Medical Review and provide support to the team where necessary to ensure regulatory compliance.
8. Participate in audits and inspections as required.
9. Ensure understanding of client needs and ensure expectations are met and exceeded.
10. Organise team meetings as requested.

Education and Experience:

Education: Pharmacy graduate

Minimum 5-10 years experience working for service providers.

Previous experience in data entry, management, or pharmacovigilance (preferably 5+ years).

Technical Skills:

Proficiency in Microsoft Office and familiarity with PV databases (e.g., Argus, ArisG).

Knowledge:

Understanding of GVP and regulatory standards related to pharmacovigilance.

Skills:

• Sense of priorities
• Team Management
• Organization skills
• Team Spirit
• Methodical
• Communicant
• Ability to make decisions
• Rigour
• Adaptability
• Microsoft Office
• Fluent in both English and French (Oral and Written)

Additional notes: Please note that if you are NOT a passport holder of the country for the vacancy, you might need a work permit. Check our Blog for more information. Bank or payment details should not be provided when applying for a job. Eurojobs.com is not responsible for any external website content. All applications should be made via the 'Apply now' button.