![PrimeVigilance](https://media.trabajo.org/img/noimg.jpg)
Senior Pharmacovigilance Associate
2 meses atrás
**Company Description**
We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.
PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device.
We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved.
Come and join us in this exciting journey to make a positive impact in patient’s lives.
At PrimeVigilance, Senior PV Associates are experienced case processing team members who are expected to manage a variety of case processing services with mínimal guidance from senior team members.
If you join PrimeVigilance, you can expect to work with teams of different sizes, from small clinical trial, to large, generic post-marketing teams. We are always looking for proactive, capable and motivated individuals who aim to surpass any target set in front of them. Senior PV Associates are expected to reach and maintain a high level of performance within 5 months of being assigned to an ICSR team, following onboarding completion.
Responsibilities include:
- Processing of Individual Case Safety Reports from all sources (post-marketing and clinical trials) in compliance with applicable regulations, PrimeVigilance procedures and in accordance with client specific requirements and timelines, focusing on triage, data entry, quality review and submissions workflow steps.
- Reconciliation activities for all types of received reports
- Workflow management activities
**Qualifications**
We expect:
- Life science / bio medical background - healthcare related degree (chemistry, biology, biotechnology, veterinary science) and demonstrated experience in Pharmacovigilance case processing
- ARGUS experience preferred
- Time and issue management, delegation, organization and multitasking skills with good attention to detail
- Strong interpersonal and communication skills
- Fluency in English skills, both verbal and written, at least B2
**Additional Information**
We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.
To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us.
We offer:
- Training and career development opportunities internally
- Strong emphasis on personal and professional growth
- Friendly, supportive working environment
- Opportunity to work with colleagues based all over the world, with English as the company language
Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join
- Quality
- Integrity & Trust
- Drive & Passion
- Agility & Responsiveness
- Belonging
- Collaborative Partnerships
Temos outros empregos actuais relacionados com esta área que pode encontrar abaixo
-
Associate Pharmacovigilance
Há 6 dias
Porto, Porto, Portugal Bial Tempo inteiroJoin Our Mission to Improve Lives Worldwide The Associate Pharmacovigilance & Drug Safety Specialist will collaborate in implementing BIAL Pharmacovigilance and Drug Safety system during clinical development, post authorization and commercialization phases, in compliance with the applicable legislation.The Impact You'll Make - Collaborate in the...
-
Porto, Porto, Portugal Bial Tempo inteiroCareer Opportunities:Associate Pharmacovigilance & Drug Safety Specialist Requisition ID Posted PortugalPorto Join Our Mission to Improve Lives Worldwide The Associate Pharmacovigilance & Drug Safety Specialist will collaborate in implementing BIAL Pharmacovigilance and Drug Safety system during clinical development, post authorization and commercialization...
-
Associate Pharmacovigilance
Há 6 dias
Porto, Porto, Portugal Bial Tempo inteiroJoin Our Mission to Improve Lives WorldwideThe Associate Pharmacovigilance & Drug Safety Specialist will collaborate in implementing BIAL Pharmacovigilance and Drug Safety system during clinical development, post authorization and commercialization phases, in compliance with the applicable legislation.The Impact You'll Make Collaborate in the establishment...
-
Associate Pharmacovigilance
Há 6 dias
Porto, Porto, Portugal Bial Tempo inteiroJoin Our Mission to Improve Lives WorldwideThe Associate Pharmacovigilance & Drug Safety Specialist will collaborate in implementing BIAL Pharmacovigilance and Drug Safety system during clinical development, post authorization and commercialization phases, in compliance with the applicable legislation.The Impact You'll Make Collaborate in the establishment...
-
Porto, Porto, Portugal Bial Tempo inteiroCareer Opportunities: Associate Pharmacovigilance & Drug Safety Specialist (3970)Requisition ID Posted - Portugal - PortoJoin Our Mission to Improve Lives Worldwide The Associate Pharmacovigilance & Drug Safety Specialist will collaborate in implementing BIAL Pharmacovigilance and Drug Safety system during clinical development, post authorization and...
-
Associate Pharmacovigilance
3 semanas atrás
Porto, Portugal Bial Tempo inteiro**Join Our Mission to Improve Lives Worldwide** The Associate Pharmacovigilance & Drug Safety Specialist will collaborate in implementing BIAL Pharmacovigilance and Drug Safety system during clinical development, post authorization and commercialization phases, in compliance with the applicable legislation. **The Impact You’ll Make** - Collaborate in the...
-
Associate Pharmacovigilance
3 semanas atrás
Porto, Portugal Bial Tempo inteiro**Join Our Mission to Improve Lives Worldwide** The Associate Pharmacovigilance & Drug Safety Specialist will collaborate in implementing BIAL Pharmacovigilance and Drug Safety system during clinical development, post authorization and commercialization phases, in compliance with the applicable legislation. **The Impact You’ll Make** - Collaborate in the...
-
Associate Pharmacovigilance
2 semanas atrás
Porto, Portugal Bial Tempo inteiroJoin Our Mission to Improve Lives Worldwide The Associate Pharmacovigilance & Drug Safety Specialist will collaborate in implementing BIAL Pharmacovigilance and Drug Safety system during clinical development, post authorization and commercialization phases, in compliance with the applicable legislation. The Impact You'll Make • Collaborate in the...
-
Associate Pharmacovigilance
Há 6 horas
Porto, Portugal Bial Tempo inteiroJoin Our Mission to Improve Lives WorldwideThe Associate Pharmacovigilance & Drug Safety Specialist will collaborate in implementing BIAL Pharmacovigilance and Drug Safety system during clinical development, post authorization and commercialization phases, in compliance with the applicable legislation.The Impact You'll Make• Collaborate in the...
-
Associate Pharmacovigilance
Há 6 horas
Porto, Portugal Bial Tempo inteiroJoin Our Mission to Improve Lives Worldwide The Associate Pharmacovigilance & Drug Safety Specialist will collaborate in implementing BIAL Pharmacovigilance and Drug Safety system during clinical development, post authorization and commercialization phases, in compliance with the applicable legislation.The Impact You'll Make - Collaborate in the...
-
Porto, Portugal Bial Tempo inteiroCareer Opportunities: Associate Pharmacovigilance & Drug Safety Specialist (3970) Requisition ID 3970 - Posted - Portugal - Porto Join Our Mission to Improve Lives Worldwide The Associate Pharmacovigilance & Drug Safety Specialist will collaborate in implementing BIAL Pharmacovigilance and Drug Safety system during clinical development, post authorization...
-
Career Opportunities: Associate Pharmacovigilance
2 semanas atrás
Porto, Portugal Bial Tempo inteiroCareer Opportunities: Associate Pharmacovigilance & Drug Safety Specialist (3970) Requisition ID 3970 - Posted - Portugal - Porto Join Our Mission to Improve Lives Worldwide The Associate Pharmacovigilance & Drug Safety Specialist will collaborate in implementing BIAL Pharmacovigilance and Drug Safety system during clinical development, post...
-
Porto, Portugal Bial Tempo inteiroCareer Opportunities: Associate Pharmacovigilance & Drug Safety Specialist (3970) Requisition ID 3970 - Posted - Portugal - PortoJoin Our Mission to Improve Lives WorldwideThe Associate Pharmacovigilance & Drug Safety Specialist will collaborate in implementing BIAL Pharmacovigilance and Drug Safety system during clinical development, post...
-
Associate Pharmacovigilance
2 meses atrás
Porto, Portugal Bial Tempo inteiro**MISSION** Collaborate in implementing and within the management of BIAL Pharmacovigilance and drug safety system during clinical development, post authorization and commercialization phases, in compliance with the applicable legislation. **MAIN ATTRIBUTIONS AND RESPONSIBILITIES** - Collaborate in the establishment of a Pharmacovigilance network of BIAL in...
-
Career Opportunities: Pharmacovigilance
Há 6 dias
Porto, Porto, Portugal Bial Tempo inteiroCareer Opportunities: Pharmacovigilance & Drug Safety Manager (3916) Requisition ID 3916 - Posted - Portugal - Porto Join Our Mission to Improve Lives WorldwideReporting to the Director, Pharmacovigilance & Drug Safety, the Pharmacovigilance & Drug Safety Manager maintains BIAL Pharmacovigilance and drug safety system during clinical development, post...
-
Career Opportunities: Pharmacovigilance
2 semanas atrás
Porto, Portugal Bial Tempo inteiroCareer Opportunities: Pharmacovigilance & Drug Safety Manager (3916) Requisition ID 3916 - Posted - Portugal - Porto Join Our Mission to Improve Lives Worldwide Reporting to the Director, Pharmacovigilance & Drug Safety, the Pharmacovigilance & Drug Safety Manager maintains BIAL Pharmacovigilance and drug safety system during clinical development, post...
-
Career Opportunities: Pharmacovigilance
Há 6 horas
Porto, Portugal Bial Tempo inteiroCareer Opportunities: Pharmacovigilance & Drug Safety Manager (3916) Requisition ID 3916 - Posted - Portugal - Porto Join Our Mission to Improve Lives Worldwide Reporting to the Director, Pharmacovigilance & Drug Safety, the Pharmacovigilance & Drug Safety Manager maintains BIAL Pharmacovigilance and drug safety system during clinical development, post...
-
Career Opportunities: Pharmacovigilance
Há 6 horas
Porto, Portugal Bial Tempo inteiroCareer Opportunities: Pharmacovigilance & Drug Safety Manager (3916) Requisition ID 3916 - Posted - Portugal - Porto Join Our Mission to Improve Lives WorldwideReporting to the Director, Pharmacovigilance & Drug Safety, the Pharmacovigilance & Drug Safety Manager maintains BIAL Pharmacovigilance and drug safety system during clinical development, post...
-
Pv Associate
3 semanas atrás
Porto, Portugal PrimeVigilance Tempo inteiroCompany Description We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs...
-
Pv Associate
Há 5 dias
Porto, Portugal PrimeVigilance Tempo inteiroCompany Description We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs...