17 Jobs für Pharmacovigilance Associate
Stellenangebote Pharmacovigilance Associate Jobs
Job vor 2 Tagen bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The
Associate Medical Director/ Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on assigned trials. Serve as a medical expert during project delivery lifecycle. Provide therapeutic and medical expertise to business development activities. Essential Functions The [. .. ] Adverse Events (AEs) . # # May perform medical case review of Serious Adverse Events (SAEs) , including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. # # May provide medical support for the Analysis of Similar Events (AOSE) , in collaboration with or on behalf of Pharmacovigilance department. # # May perform medical review of adverse event coding. # # Performs review of the Clinical Study Report (CSR) and patient narratives. [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Medical Director-Psychiatry (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Job Overview The
Associate Medical Director/ Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. They will participate in all aspects of medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] science involvement on assigned trials, serve as a medical expert during the project delivery lifecycle, and provide therapeutic and medical expertise to business development [. .. ] of trial-related Adverse Events (AEs) . May perform medical case review of Serious Adverse Events (SAEs) , including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. May provide medical support for the Analysis of Similar Events (AOSE) , in collaboration with or on behalf of Pharmacovigilance department. May perform medical review of adverse event coding. Performs review of the Clinical Study Report (CSR) and patient narratives. Attends Kick-Off meetings, weekly team meetings, and client [. .. ]
Job vor 2 Tagen bei Jooble gefunden
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern
[. .. ] protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete via review of site source documents and medical records. [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with project site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates, and may, with supervision, lead, global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends [. .. ]
Job vor 2 Tagen bei Jooble gefunden
Veeva Systems
• Berlin
Beratungs-/ Consultingtätigkeiten
[. .. ] tangible business value. R D Business Consulting supports biopharma, medtech, animal and consumer health customers with solving business problems across the R D value chain but also [...]
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[...] specifically within Clinical, Pharmacovigilance and Regulatory domains. You will be part of a global team delivering meaningful and high-impact projects with a variety of organisations from Top 20 Pharma to small/ mid-sized organisations. What Youll Do Lead project workstreams from end-to-end, ensuring the high-quality design and delivery of customer solutions Solve complex problems for Life Sciences leaders, leveraging Veevas unique data and software insights Mentor and manage Associate Consultants, overseeing their work and professional development within your workstream Drive practice growth by contributing to business development and internal IP creation Requirements Experience: 3+ years in Life Sciences Consulting (Business or Management Consulting preferred) Domain Knowledge: Proven expertise in Clinical Data/ Operations, Regulatory or Pharmacovigilance/ Drug Safety Analytical Rigor: [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Biontech
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
As
Associate Director Audit Management, you will play a pivotal role in ensuring the quality and compliance of Bio NTechs clinical trials and processes. As part of the Global Development [...]
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[...] Quality Assurance team, you will lead audits across Good Clinical Practice (GCP) , Good Laboratory Practices (GLP) , Good Pharmacovigilance Practice (GVP) , and Information Technology (IT) domains. Your work will directly contribute to advancing Bio NTechs mission by ensuring adherence to regulatory standards and fostering continuous improvement in clinical development activities. Your Contribution: Lead global audits with a focus on clinical investigator sites and vendor audits in the EU, UK, [. .. ]
Job vor 5 Tagen bei Jooble gefunden
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern
[. .. ] protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Applies query resolution techniques remotely and on site, and [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according [. .. ]
Job am 15.04.2026 bei Jooble gefunden
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
[. .. ] protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Applies query resolution techniques remotely and on site, and [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according [. .. ]
Job am 15.04.2026 bei Jooble gefunden
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
[. .. ] protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete via review of site source documents and medical records. [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with project site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates, and may, with supervision, lead, global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Veeva Systems
• Berlin Berlin, DE
Beratungs-/ Consultingtätigkeiten
[. .. ] of choice for 85 of the top 20 Pharmaceutical companies, to define and realize the strategic value of Regulatory Affairs, Clinical Strategy Operations as well as Quality [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and Safety (eg. Pharmacovigilance) . As a Consultant, you will manage workstreams on consulting projects for Veeva customers in R D planning, organizing, and tracking all aspects of delivery. You will analyze problems, build insightful solutions, and develop close working relationships with customer stakeholders (through face-to-face discussions, workshops, email, etc. ) to [. .. ] the customer Be a primary client contact for operational project questions, developing the relationship through face-to-face discussions, workshops, phone, and email contact Manage the work and priorities of Associate Consultants in your workstream Support and mentor Associates in developing skills and professional capabilities Build trusted relationships with customer stakeholders Bring to your customers a good level of industry/ market/ functional insights Input into business development opportunities and proposals Help develop and disseminate thought leadership Requirements Bachelor s or Masters [. .. ]
Job am 08.04.2026 bei Jooble gefunden
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
[. .. ] protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Applies query resolution techniques remotely and on site, and [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Biontech
Associate Director, Safety Scientist
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
The
Associate Director, Safety Sciences provides scientific expertise for medical safety tasks. Core responsibilities include safety data review and analysis from different sources, periodic report authoring and the oversight [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of the safety surveillance activities for the assigned program (s) . The Safety Scientist ensures that all processes are conducted according to Bio NTech [. .. ] inspections for key safety processes such as Safety Surveillance and aggregate report generation A Good Match: Advanced degree in life sciences/ healthcare; Ph D in a relevant discipline or post-doctoral pharmacovigilance certification preferred At least 5 years of experience in clinical research with significant exposure to pharmacovigilance activities within biotech/ pharmaceutical industries or CROs Expert knowledge of pharmacovigilance laws/ regulations as well as GCP/ GVP guidelines Proven experience in designing and implementing clinical safety processes/ tools and assessing/ reporting safety data [. .. ]
Job am 08.04.2026 bei Jooble gefunden
CRA-Future Roles (Germany)
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
[. .. ] protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] deviation/ violations and pharmacovigilance issues. For the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes Conducts Source Document Review of appropriate site source documents and medical records Verifies required clinical data entered in the case report form (CRF) is accurate and complete Applies query resolution techniques remotely and on site, and [. .. ] oversight of the Lead CRA, to changing priorities to achieve goals/ targets. May act as primary liaison with project site personnel, or in collaboration with another CRA or Central Monitoring Associate (CMA) . Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Projektmitarbeiter der Geschäftsführung (m/w/d) Vollzeit in München
• München, Bayern
Führungs-/ Leitungspositionen Homeoffice möglich Abgeschlossenes Studium
Betriebliche Altersvorsorge
[. .. ] type Full-time Job function Job function Project Management Industries Professional Services Referrals increase your chances of interviewing at BONAGO Incentive Marketing Group by 2x Get notified about [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] new Project Associate jobs in Munich, Bavaria, Germany. Junior Project Manager/ PMO (all genders) Team Assistant Project Coordinator (m/f/x) Corporate Communications Europe Team Tester for a car voice assistant project-English (Australian) speaker Junior Program Manager/ Junior Projektmanager Automotiv (all gender) Team Assistant Project Coordinator (m/f/x) Corporate Communications Europe Team Project Assistant-Clinical Safety Pharmacovigilance (office based in Munich) Supply Chain Project Coordinator (m/f/d) Product Process Support Tester for a car voice assistant project-Spanish (Spain) speaker JUNIOR PROJEKT LEITER/in (m/w/d) Event Promotion Junior Projektmanager Elektrotechnik (all gender) Working Student Smart Site Operations Strategy (m/f/d) Intern Sustainability Management [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Sr CRA Oncology Germany
• München, Bayern
[. .. ] protecting the confidentiality of each subject/ patient. Assesses factors that might affect subject/ patients safety and clinical data integrity at an investigator/ physician site such as protocol [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] deviation/ violations and pharmacovigilance issues. Per the Clinical Monitoring/ Site Management Plan (CMP/ SMP) : Assesses site processes. Conducts Source Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete via review of site source documents and medical records. [. .. ] are met. Must be able to quickly adapt to changing priorities to achieve goals/ targets. May act as primary liaison with project site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements. Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates, and may, with supervision, lead, global clinical monitoring/ project staff meetings (inclusive of Sponsor representation, as applicable) and attends [. .. ]
Job am 26.03.2026 bei Jobleads gefunden
Business Consultant-R D (Remote)
• Berlin
Beratungs-/ Consultingtätigkeiten
[. .. ] of choice for 85 of the top 20 Pharmaceutical companies, to define and realize the strategic value of Regulatory Affairs, Clinical Strategy Operations as well as Quality [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and Safety (eg. Pharmacovigilance) . As a Consultant, you will manage workstreams on consulting projects for Veeva customers in R D planning, organizing, and tracking all aspects of delivery. You will analyze problems, build insightful solutions, and develop close working relationships with customer stakeholders (through facetoface discussions, workshops, email, etc. ) to deliver demonstrable, [. .. ] faced by the customer Be a primary client contact for operational project questions, developing the relationship through facetoface discussions, workshops, phone, and email contact Manage the work and priorities of Associate Consultants in your workstream Support and mentor Associates in developing skills and professional capabilities Build trusted relationships with customer stakeholders Bring to your customers a good level of industry/ market/ functional insights Input into business development opportunities and proposals Help develop and disseminate thought leadership Requirements Bachelors or Masters degree [. .. ]
Job am 02.03.2026 bei Jobleads gefunden
Associate Director, Medical Affairs Amyloidosis
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] the development of a deep understanding of the respective indication area. Acquisition of sufficient knowledge of current local regulations of the pharmaceutical industry and collaboration with the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Regulatory Affairs department, Pharmacovigilance department, Quality Assurance, Legal, Commercial Department and all other company divisions. You Will Need To Have University degree in medicine (preferred) , pharmacy, or biology, Ph D desirable 5-8 years of experience in the pharmaceutical/ biotechnology industry in medical affairs Strong leadership skills and the ability to motivate teams Proven [. .. ]
Job am 20.11.2025 bei Jobleads gefunden
Manager (w/m/d) Regulatory Affairs Biocides
• Köln, Nordrhein- Westfalen
[. .. ] Menschen an und setzen uns dafür ein, unsere Mitarbeitenden bei der Entwicklung ihres individuellen Potenzials zu unterstützen. Bitte richten Sie Ihre Bewerbung an das Recruiting Team. Seniority [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] level Seniority level Associate Employment type Employment type Full-time Job function Job function Other Industries Chemical Manufacturing Referrals increase your chances of interviewing at LANXESS by 2x Get notified about new Manager (w/m/d) Regulatory Affairs Biocides jobs in Cologne, North Rhine-Westphalia, Germany. Cologne, North Rhine-Westphalia, Germany 3 weeks ago [. .. ] ago Cologne, North Rhine-Westphalia, Germany 2 weeks ago Regulatory Affairs-Labelling Specialist (w/m/d) Langenfeld, North Rhine-Westphalia, Germany 2 weeks ago Global ICT Business Partner (Regulatory Affairs Pharmacovigilance) Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr 70115425 [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Pharmacovigilance Associate pro Jahr?
Als Pharmacovigilance Associate verdient man zwischen EUR 50.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmacovigilance Associate Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 17 offene Stellenanzeigen für Pharmacovigilance Associate Jobs.
In welchen Bundesländern werden die meisten Pharmacovigilance Associate Jobs angeboten?
Die meisten Stellenanzeigen für Pharmacovigilance Associate Jobs werden derzeit in Bayern (9 Jobs), Nordrhein-Westfalen (4 Jobs) und Berlin (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmacovigilance Associate Jobs?
Pharmacovigilance Associate Jobs gehören zum Berufsfeld Pharmazie.
