Pharmacovigilance Specialist
3 semanas atrás
**Main Responsibilities**:
- Responsible for day-to-day adverse experience case management within the Portugal including case intake and follow-up activities in accordance with Global Safety procedures, the review of local literature as per Client's procedure and country regulations, and health authority submissions of cases in accordance with Global Safety procedures and health authority requirements.
- Responsible for the reconciliation of adverse events reports received from other Client operating units (e.g., Designated Point of Contact, Medical Information, etc.) and contractual partners, as applicable.
- Review market research questionnaires prior and post study occurrence.
- Assist in preparation for audits / inspections for their country / territories and may participate in the audit and / or inspection.
- Identify and communicate potential safety issues to pharmacovigilance specialist Country Lead.
- Complete and document required pharmacovigilance specialist training within the required timelines.
- Liaise with Data Management Centers and Global Safety Global Case Management colleagues at HQ.
**Main Requirements**:
- A health, life science, or medical science degree or equivalent by education/experience.
- A minimum 2 years of pharmaceutical industry experience (ideally at least 1 year in PV).
- An awareness of Pharmacovigilance regulations and PV Quality assurance.
- Strong communication and time management skills and have the ability to work independently with mínimal supervision.
- Excellent written & spoken English.
- Proficiency in good documentation practices.
- Familiar with the use of a safety database.
**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
-
Senior Pharmacovigilance Specialist
2 semanas atrás
Lisboa, Lisboa, Portugal Med Communications International Tempo inteiroSenior Pharmacovigilance Specialist - Remote Lisboa Senior Pharmacovigilance Specialist - RemoteLisboa Lisbon, Lisbon, Portugal Senior Pharmacovigilance Specialist - Remote Highlights: Pre and post marketing PV experience PV Planning in clinical trialsRMP writing POSITION SUMMARY The Senior Pharmacovigilance Specialist is a professional with scientific,...
-
Senior Pharmacovigilance Specialist
2 semanas atrás
Lisboa, Lisboa, Portugal Tn Portugal Tempo inteiroSenior Pharmacovigilance Specialist - Remote Lisboa Senior Pharmacovigilance Specialist - RemoteLisboa Lisboa, Lisboa, Portugal col-wideJob Description:Senior Pharmacovigilance Specialist - RemoteHighlights:Pre and post marketing PV experiencePV Planning in clinical trialsDSUR, PSUR/PBRERRMP writingPOSITION SUMMARYThe Senior Pharmacovigilance Specialist is a...
-
Senior Pharmacovigilance Specialist
2 semanas atrás
Lisboa, Lisboa, Portugal Med Communications International Tempo inteiroSenior Pharmacovigilance Specialist - RemotePOSITION SUMMARY The Senior Pharmacovigilance Specialist is a professional with scientific, clinical, and therapeutic area expertise responsible for case management activities, expedited/non-expedited reporting activities, periodic reporting activities, risk management, signal detection and surveillance, ad-hoc...
-
Senior Pharmacovigilance Specialist
Há 5 dias
Lisboa, Portugal Med Communications International Tempo inteiro.Senior Pharmacovigilance Specialist - Remote Lisboa Senior Pharmacovigilance Specialist - RemoteLisboa Lisbon, Lisbon, Portugal Senior Pharmacovigilance Specialist - Remote Highlights: Pre and post marketing PV experience PV Planning in clinical trialsRMP writing POSITION SUMMARY The Senior Pharmacovigilance Specialist is a professional with scientific,...
-
Pharmacovigilance Specialist
2 semanas atrás
Lisboa, Lisboa, Portugal Labcorp Tempo inteiroMain Responsibilities: Responsible for daytoday adverse experience case management within the Portugal including case intake and followup activities in accordance with Global Safety procedures, the review of local literature as per Client's procedure and country regulations, and health authority submissions of cases in accordance with Global Safety...
-
Pharmacovigilance Submission Specialist
2 semanas atrás
Lisboa, Lisboa, Portugal Prime Vigilance Ltd Tempo inteiroWe are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially 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...
-
Senior Pharmacovigilance Specialist
Há 5 dias
Lisboa, Portugal Med Communications International Tempo inteiroSenior Pharmacovigilance Specialist - Remote Lisboa Senior Pharmacovigilance Specialist - Remote Lisboa Lisbon, Lisbon, Portugal Senior Pharmacovigilance Specialist - Remote Highlights:Pre and post marketing PV experiencePV Planning in clinical trialsRMP writingPOSITION SUMMARYThe Senior Pharmacovigilance Specialist is a professional with scientific,...
-
Senior Pharmacovigilance Specialist
Há 5 dias
Lisboa, Portugal Med Communications International Tempo inteiroSenior Pharmacovigilance Specialist - Remote Lisboa Senior Pharmacovigilance Specialist - RemoteLisboaLisbon, Lisbon, Portugal Senior Pharmacovigilance Specialist - RemoteHighlights:Pre and post marketing PV experiencePV Planning in clinical trialsRMP writingPOSITION SUMMARYThe Senior Pharmacovigilance Specialist is a professional with scientific, clinical,...
-
Junior Pharmacovigilance Specialist
3 semanas atrás
Lisboa, Portugal Fortrea - Organic Tempo inteiroAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
Pharmacovigilance Submission Specialist
Há 5 dias
Lisboa, Portugal Prime Vigilance Ltd Tempo inteiroWe are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially 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...
-
Pharmacovigilance Submission Specialist
4 semanas atrás
Lisboa, Portugal Primevigilance Tempo inteiroWe are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially 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...
-
Pharmacovigilance Submission Specialist
4 semanas atrás
Lisboa, Portugal Primevigilance Tempo inteiroWe are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially 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...
-
Pharmacovigilance Submission Specialist
Há 2 dias
Lisboa, Portugal PrimeVigilance Tempo inteiro**Company Description** We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially 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,...
-
Pharmacovigilance Submission Specialist
2 semanas atrás
Lisboa, Lisboa, Portugal Primevigilance Tempo inteiroWe are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially 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...
-
Pharmacovigilance Submission Specialist
2 semanas atrás
Lisboa, Lisboa, Portugal PrimeVigilance Tempo inteiroCompany DescriptionWe are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially 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...
-
Sr Quality Assurance Specialist- FSP Team
2 semanas atrás
Lisboa, Lisboa, Portugal LIS Fortrea Development Ltd Sucursal em Portugal Tempo inteiroAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
Lisboa, Portugal Organon Tempo inteiro.Senior Specialist, Quality Assurance Auditor Lisboa Senior Specialist, Quality Assurance AuditorLisboa Lisboa, Lisboa, Portugal Job Description The Position The Senior Specialist, Quality Assurance Auditor, ensures quality and compliance with local and international regulatory requirements by conducting internal and external audits. This role provides...
-
Quality and Compliance Training Specialist
4 semanas atrás
Lisboa, Portugal Ergomed Tempo inteiro**Company Description** Ergomed Group is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia Our company allows for employee visibility...
-
Quality and Compliance Training Specialist
2 meses atrás
Lisboa, Portugal Ergomed Tempo inteiro**Company Description** Ergomed Group is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia Our company allows for employee visibility...
-
Medical Affairs Specialist
2 semanas atrás
Lisboa, Portugal Kenvue Tempo inteiro**Medical Affairs Specialist**-2307006941W Description At Kenvue, we believe there is extraordinary power in everyday care. Built on over a century of heritage and propelled forward by science, our iconic brands—including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® —are category leaders trusted by millions of consumers...
