Senior Pharmacovigilance Physician

Ergomed; Barcelona; Presencial; EUR 50.000 - 90.000; Jornada completa

Descripción de la vacante

An established industry player is seeking a Senior Pharmacovigilance Physician to join their dynamic team. In this pivotal role, you will be responsible for the medical review of individual case safety reports, signal detection, and mentoring junior physicians. The company prides itself on fostering a supportive and inclusive work environment, emphasizing personal and professional growth. You will collaborate with a global team, contributing to important safety assessments and regulatory submissions. If you are passionate about improving patient safety and thrive in a collaborative setting, this opportunity is perfect for you.

Servicios

Training and career development opportunities

Strong emphasis on personal and professional growth

Friendly, supportive working environment

Opportunity to work with international colleagues

Formación

• Medically qualified physician with experience in pharmacovigilance.
• Expertise in signal detection and aggregate report review.

Responsabilidades

• Review and approve post-marketing Individual Case Safety Reports.
• Mentor junior PV Physicians and support QPPV in safety issues.
• Participate in signal detection and risk evaluation processes.

Conocimientos

Pharmacovigilance

Signal Detection

Medical Review

Interpersonal Skills

Communication Skills

Presentation Skills

Organizational Skills

Teamwork

English (Advanced)

Educación

Medical Degree

Herramientas

MS Office

Descripción del empleo

Company Description

We are PrimeVigilance (part of Ergomed Group), 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 Assurance.

PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and becoming one of the global leaders in its fields. We cover all therapy areas including medical devices.

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.

Job Description

The Senior Pharmacovigilance (PV) Physician I is responsible for medical review of ICSRs, writing and/or reviewing signal detection reports, writing and/or reviewing aggregate reports (DSURS, PSURS, PBRERs, PADERS), reviewing risk management reports (RMPs) and mentoring junior PV Physicians. The Senior PV Physician I is also expected to support the QPPV in medical aspects and safety issues as may be required by Company or Client.

For the Client

1. To review and approve post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports for medical/causality assessment. Review includes coding, assessment of seriousness, listedness/expectedness and Company causality, as well as writing of Company comment, follow-up questions and Analysis of Similar Events, when required, including completion of all required supporting documentation such as trackers.
2. To complete the adverse event tracker for all ICSRs reports.
3. To act as a Qualified Person for Pharmacovigilance or support the Qualified Person for Pharmacovigilance (if not medically qualified) in the medical understanding and evaluation of any safety issues.
4. To review and approve literature screening search strategy.
5. To review articles to determine if they contain ICSRs/SAEs related to the relevant Medicinal Product or other safety related findings.
6. To cooperate in the preparation of and provide input in Risk Management Plans.
7. Supporting/to lead the preparation of responses to regulatory authority requests.
8. Can act as EEA QPPV and/or Deputy for up to 2 clients if required.
9. To review and provide input in Periodic Safety Update Reports, Development Safety Update Reports, ACOs or Annual Safety Reports.
10. To act as Company Lead in a specific pharmacovigilance area requiring medical input (e.g. for preparation of reference safety information – Company Core Data Sheet).
11. Actively participate in the Drug Safety Review Committee - signal detection and risk evaluation process for Client company medicinal products in the product's life cycle. Serves on Client’s advisory and scientific committees.

Signalling

1. Participating in signal detection activities including meetings, reviewing of signal detection reports, and providing consultation to clients on aspects related to benefit/risk assessment and risk minimisation.
2. Evaluating and categorizing possible signals.
3. Proposing a course of action whenever a possible signal is identified.
4. Supporting preparation and review of benefit-risk reports.
5. Supporting PV Project Managers in the planning of signalling schedule and resources.
6. Supporting PV Project Managers in the preparation of project-specific working instructions regarding signalling.
7. Overseeing the quality of signal detection activities and providing quality and compliance metrics to the Quality Department.

For the Company

1. To support the preparation of PV procedures.
2. To provide training and mentoring of junior PV Physicians.
3. To provide medical advice and input to project teams on a daily basis.
4. Training, mentoring and managing junior PV Physicians.
5. Continuously working on the development of the procedures on the company level.
6. Preparing or contributing to the preparation of signalling related company procedures.
7. The Senior PV Physician will support the Director of Projects, as well as the QPPV, on a day-to-day basis as needed.
8. Supporting the Medical Director in training and mentoring on signalling activities.

Qualifications

• The PV Physician should be medically qualified as a physician.
• Previous experience in pharmacovigilance.
• Ability to review different aggregate report types including PBRERs and DSURs.
• Expertise in signal detection activities is essential.
• Excellent interpersonal skills.
• Ability to plan, organise, prioritise and execute multiple tasks.
• Ability to work effectively cross-culturally and cross-functionally and value the importance of teamwork.
• Communication skills.
• Presentation skills.
• English - advanced (spoken, written).
• Advanced literacy (MS Office).

Additional Information

Why PrimeVigilance

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

Come and join us in this exciting journey to make a positive impact in patient’s lives. We look forward to welcoming your application.