Job Details: Pharmacovigilance Officer


JobsIreland
Jervis Street
Dublin 1
jobsireland.ie
Pharmacovigilance Officer
Essential requirements:

* Degree level qualification in a clinical or life sciences related
subject.

* Proven project management and organisational skills.

* Five years&#**Apply on the website**; experience gained working in
clinical research or a closely related field in the commercial (e.g.
CRO, Pharma sector) or academic setting.

* Must have experience gained working in a vigilance role (Pharmaco or
Device vigilance) for a sponsor in a commercial (e.g. CRO, Pharma) or
academic setting.

* Experience in developing vigilance strategies and safety data
management.

* Excellent communication skills (oral, written & presentation) with
proven ability to work effectively as part of a team.

* Strong leadership and communication skills.

* Self-motivated and able to work independently, showing initiative
and good judgement.

* Good data management and IT skills.

Desirable skills:

* At least one year experience gained working directly in a
Pharmacovigilance role for a sponsor in a commercial (e.g. CRO,
Pharma) or academic setting.

* Qualification in Pharmacovigilance or related discipline leading the
development of safety plans and strategies for safety oversight of
clinical study execution

* Postgraduate Qualification in Clinical Research or other Life
Science or engineering-related subject

* Prior experience in Pharmacovigilance of academic-Sponsored clinical
studies

* Understanding of MedDRA coding

* Familiarity with medical and therapeutic area knowledge terminology

* Understanding of EudraVigilance reporting processes.

* Clinical Research Data Management experience

* Experience working with EDC systems for data capture and design of
Safety Case Report Forms.

* Good Clinical Practice training.

For a complete and comprehensive job description please get in touch Essential requirements:

* Degree level qualification in a clinical or life sciences related
subject.

* Proven project management and organisational skills.

* Five years&#**Apply on the website**; experience gained working in
clinical research or a closely related field in the commercial (e.g.
CRO, Pharma sector) or academic setting.

* Must have experience gained working in a vigilance role (Pharmaco or
Device vigilance) for a sponsor in a commercial (e.g. CRO, Pharma) or
academic setting.

* Experience in developing vigilance strategies and safety data
management.

* Excellent communication skills (oral, written & presentation) with
proven ability to work effectively as part of a team.

* Strong leadership and communication skills.

* Self-motivated and able to work independently, showing initiative
and good judgement.

* Good data management and IT skills.

Desirable skills:

* At least one year experience gained working directly in a
Pharmacovigilance role for a sponsor in a commercial (e.g. CRO,
Pharma) or academic setting.

* Qualification in Pharmacovigilance or related discipline leading the
development of safety plans and strategies for safety oversight of
clinical study execution

* Postgraduate Qualification in Clinical Research or other Life
Science or engineering-related subject

* Prior experience in Pharmacovigilance of academic-Sponsored clinical
studies

* Understanding of MedDRA coding

* Familiarity with medical and therapeutic area knowledge terminology

* Understanding of EudraVigilance reporting processes.

* Clinical Research Data Management experience

* Experience working with EDC systems for data capture and design of
Safety Case Report Forms.

* Good Clinical Practice training.

For a complete and comprehensive job description please get in touch

We need : English (Good)

Type: Permanent
Payment:
Category: Others

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