Local PV Officer Consultant

Reposted 13 Days Ago
Be an Early Applicant
Hiring Remotely in France
Remote
Mid level
Pharmaceutical
The Role
The Area Safety Officer manages safety activities for compliance with regulations and policies, oversees training, audits, and reporting while coordinating with stakeholders.
Summary Generated by Built In

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….

 

ClinChoice is searching for an Area/Local Safety Officer Consultant for 12 months Contract with possibility of extension to join one of our clients.

Work from the office in Issy-les-Moulineaux, France. is required a minimum of 2 days/week. The individual can work from home the other days of the week.

The Area Safety Officer is responsible for ensuring that the local operating company (LOC) Safety activities related to all products are managed in compliance with local regulations and company policies/procedures at a local, regional, and global levels and in accordance with any product vigilance agreements with third party business partners.

ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.  

 

Main Job Tasks and Responsibilities:

 

Safety and PV System Management

  • Perform the quality check of the PV cases and ensure that the English translation has been properly performed.
  • Keep up to date a local tracker of the individual safety reports.
  • Be the subject matter expert at local level on the case management activities.
  • Closely follow the respect of the regulatory timelines of the submission of the safety reports to the local health authorities and communicate any potential delay to the appropriate teams.
  • Establish and maintain local indicators on the compliance of the safety reports submission.
  • Oversee the training of the local employees and the business partners. Maintain KPI and present them during regular team meetings.
  • Perform regulatory monitoring for impact on vigilance activities and responsibilities.
  • Perform reconciliation with other departments (distributors, third parties, vendors, and internal stakeholders).
  • Maintain oversight of proper identification of local literature articles for AE reporting as required.
  • Perform reporting/ submissions of safety reports/ updates/information (e.g., SAE, SUE, SUSARs, PSUR, RMP) to local health authorities and other Client departments as applicable.
  • Supporting Area Safety Lead in notifying local health authorities of any safety issues including SSI/ESI and Signals.
  • Maintain up-to-date knowledge of local requirements for pharmacovigilance, cosmetic and device vigilances including reporting requirements (for all applicable product classes in the territory) and collaborating with the global team to implement process changes required for identification of new requirements.
  • Record self-identified non-conformances and collaborating with the global team to investigate non-conformances while developing and implementing effective CAPAs.
  • Perform other agreed tasks assigned by manager
  • Perform document management and archiving as required

Procedural Document

  • Ensure current knowledge of all relevant company procedures and training.
  • Develop, update, and implement local procedures to ensure compliance with Clients global procedures and national requirements.

Audit & Inspection readiness

Support in local health authority inspections and audits conducted locally, including responding to queries during the conduct and collaborating with the global team to develop and implement CAPA (Corrective and Preventative Action) plans as applicable

PV contract management

Provide PV clauses to be included within local agreements and contribute to the PSMF with contracts-related information

Business Continuity

Ensure implementation of local business continuity plans (e.g., inspection readiness, AE reporting coverage)

 

Education and Experience:

 

Education: health care science professional or equivalent training

  • Significant training in data management with strong IT skills.
  • 2-4 years of relevant experience (e.g. case data management, reconciliation manager, vigilance IT project manager…).
  • Fluent in English. French as a mother tongue.
  • Excellent communication skills and ability to work with cross-functional teams.
  • Rigor is a key skill for this mission.

 

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

 

Who will you be working for?

 

About ClinChoice    

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.           

 

Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are  the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology.   The success of these core values is evidenced by our below industry average turnover rates.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.

 

Key words: Area Safety Officer, Local Safety Officer, PV, QC, CAPA,QPPV

 

#LI-PB1


Skills Required

  • Education in health care science or equivalent training
  • 2-4 years of relevant experience in data management or vigilance
  • Fluency in English and French
  • Strong IT skills
  • Excellent communication skills

ClinChoice Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ClinChoice and has not been reviewed or approved by ClinChoice.

  • Flexible Benefits Flexible arrangements, including telecommuting and flextime with no core hours in some regions, are highlighted for many roles. Feedback suggests flexibility is commonly available but depends on role and location.
  • Leave & Time Off Breadth Vacation, personal, and sick days are part of the core package, with some markets granting paid leave from the date of hire. Feedback suggests time off is standard-to-decent across locations, though specifics vary.
  • Healthcare Strength Health coverage is positioned as a core benefit, with some accounts describing overall benefits as full or good. In the U.S., healthcare sits within a conventional CRO package alongside medical, dental, and vision.

ClinChoice Insights

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The Company
Horsham, Pennsylvania
5,000 Employees
Year Founded: 1995

What We Do

ClinChoice is a global full-service Contract Research Organization (CRO) specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies, aiming to accelerate the development and commercialization of innovative drugs and devices.

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