Remote Jobs RockRemote Jobs Rock

Senior PV Associate

πŸ•’ 4 days ago
PharmacovigilanceICSR ProcessingICSR Follow-upSAE/SUSAR Management
Apply Now

πŸ“œ Description

  • Process Individual Case Safety Reports (ICSRs) in line with regulations, company procedures, client requirements, and timelines.
  • Perform ICSR follow-up and manage SAE/SUSAR activities, including unblinding, clinical trial reconciliation, and protocol and safety plan reviews.
  • Reconcile clinical and partner data, and handle product quality complaints in coordination with Quality Assurance.
  • Perform MedDRA and WHO coding, prepare database outputs and client reports, and support workflow and resource management.
  • Support client and internal PV processes, project team activities, and local pharmacovigilance network responsibilities as assigned.

πŸ› οΈ Requirements

  • Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance
  • Minimum 1 year of work experience in pharmacovigilance
  • Organization skills, including attention to detail and multitasking
  • Management skills, including time and issue management
  • English - advanced (spoken, written)
  • Advanced literacy (MS Office)

✨ Benefits

  • 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
  • Integrity & Trust
  • Drive & Passion
  • Agility & Responsiveness
  • Collaborative Partnerships
  • Support personal data protection and interactions with Medical Information.
Full job description

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.

Job Description

  • Providing support to other activities undertaken by the project team on behalf of the client and the company
  • Performing activities in the scope of ICSR management unit within agreed extent and timeframe (including, but not limited to):
    • Processing Individual Case Safety Reports (ICSRs) from all sources in compliance with applicable regulations, PrimeVigilance procedures and in accordance with client specific requirements and timelines
    • Performing ICSR follow up
    • SAE/SUSAR Management (unblinding, clinical trial reconciliation, protocol review, Safety Management Plan review)
    • Reconciliation (clinical, partners)
    • Personal data protection
    • Product Quality Complaint handling and interaction with Quality Assurance
    • Medical Information interaction
    • MedDRA and WHO coding
    • Database Outputs and Reports (including data for monthly reporting to clients)
    • Workflow & resource management
  • Support of PV processes related to the ICSR management within PrimeVigilance and also to clients
  • More senior colleague may perform tasks assigned as per SOP to more junior position
  • Performing activities in the scope of ICSR management unit within agreed extent and timeframe
  • Supporting the RA & PV Network Department as needed, including acting as the LCPPV (Local Contact Person for Pharmacovigilance) for the specified country and taking on the role of PRLS (Person Responsible for Local Screening) for the designated language, as agreed with the line manager

Qualifications

  • Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance
  • Minimum 1 year of work experience in pharmacovigilance
  • Organization skills, including attention to detail and multitasking
  • Management skills, including time and issue management
  • 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

We look forward to welcoming your application.

Ergomed

Senior Pharmacovigilance Associate

πŸ•’ 11 days ago
ErgomedπŸ‘₯ 501 - 1000 employees🏒 Biotechnology

Manage Individual Case Safety Reports (ICSRs) and related pharmacovigilance activities, ensuring regulatory and client requirements are met while supporting patient safety and timely safety-data reporting.

PharmacovigilanceICSR ManagementICSR Follow-upSAE/SUSAR Management

Leads clinical data management across study startup, conduct, closeout, and reporting, ensuring trial data quality and integrity while coordinating with cross-functional teams, CROs, and vendors.

Clinical Data ManagementClinical TrialsClinical Data Quality And IntegrityElectronic Data Capture (edc)
Mindoula Health

Senior Behavioral Health Integration Clinician (BHIC) & Clinical Excellence Lead

πŸ•’ 3 days ago
Mindoula HealthπŸ‘₯ 201 - 500 employees🏒 Hospital & Health Care

The Senior Behavioral Health Integration Clinician (BHIC) & Clinical Excellence Lead is a clinical leadership role that combines patient care with oversight of the Collaborative Care team to ensure high-quality behavioral health services.

Behavioral HealthCare CoordinationClinical SupervisionEvidence-based Treatment
Summit Therapeutics

Associate Director, Site Alliances and Strategy

πŸ•’ 3 days ago
Summit TherapeuticsπŸ‘₯ 201 - 500 employees🏒 Biotechnology

Develops strategic partnerships with clinical trial sites and networks while shaping Clinical Operations strategy, optimizing study start-up, and translating site insights into scalable, inspection-ready trial execution.

Clinical Trial OperationsSite Alliance StrategySite ManagementStudy Start-up
Home Instead

Lead Care Professional Atherstone and Coleshill area

πŸ•’ 3 days ago
Home InsteadπŸ‘₯ 201 - 500 employees🏒 Hospital & Health Care

Leads new-client care starts through hands-on first visits, then mentors matched care professionals and checks care quality, compliance and records in close partnership with the Registered Manager.

Home CarePerson-centred CareSafeguardingMedication Administration

Trusted by Remote Workers