Associate Case Processing Manager (Line Management position)

Posted 23 Days Ago
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Guildford, Surrey, England, GBR
Hybrid
Senior level
Biotech • Pharmaceutical
The Role
Lead and line-manage an ICSR processing team for assigned projects, oversee workflow and KPIs, support ICSR processing and 2nd QC, propose process improvements, manage deviations, act as team SME and liaise with clients to ensure quality and efficiency.
Summary Generated by Built In
Company Description

Medicine moves forward here. So will you. 

At PrimeVigilance, patient safety is not one part of the job. It is why we exist. 

We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of every decision, from early development through to post-marketing surveillance. Increasingly, the value we create is not only in processing safety data but in interpreting it: spotting the signal that matters early and turning it into insight our clients can act on. 

That work takes curious minds, problem-solvers and experts who care about getting it right. It also takes a culture worth staying for. Across Europe, North America, South America, Asia and Australia, we work in an environment built on kindness, flexibility, growth and belonging, where colleagues support one another and good ideas are heard wherever they come from. 

If you want a role with real purpose, global reach and the chance to keep growing while you help protect patients, you will feel at home here. We would love to hear from you.

Job Description

  • Leads the team responsible for ICSR management for a selected project or group of projects as Team Leader 
  • Ensures adequate distribution of tasks for assigned projects and teams and oversees the workflow process 
  • Assures and exerts of activities leading to effective cooperation with clients in the area of ICSR Management 

​​Role and Responsibilities​ 

  • Providing support to other activities undertaken by the project team on behalf of the client and the company 
  • Line Manages assigned ICSR staff 
  • Creates and maintains project specific KPIs for contracted ICSR activities (this includes optimizing procedures, trainings and any other actions to increase ICSR team efficiency) 
  • Proposes process changes to ICSR Operational Lead 
  • Manages ICSR deviations with ICSR Operational Lead support 
  • Reviews trackers and timesheet data and ensures accuracy 
  • Is involved in ICSR processing and 2nd QC of cases 
  • Operates as the assigned team SME and supports other SMEs 

Qualifications

Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance 

Extensive experience in pharmacovigilance within which demonstrated work experience in line manager role. 

  • Excellent communication (written and verbal) skills 
  • Organization skills, including attention to details and multitasking 
  • Delegation skills 
  • Planning and time management 
  • Technical skills 
  • Team working 

Additional Information

When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.  

We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here. 

  • Quality: we hold ourselves to the standard patients deserve. 
  • Integrity and trust: we do the right thing, especially when it is hard. 
  • Drive and passion: we care about the outcome, because someone is waiting on it. 
  • Agility and responsiveness: we move quickly, because patients cannot wait. 
  • Belonging: everyone is welcome, and every voice counts. 
  • Collaborative partnerships: we go further by going together. 

We look forward to welcoming your application. 

Skills Required

  • Life science degree (pharmacy, nursing) or healthcare-related qualification OR pharmacovigilance experience
  • Extensive pharmacovigilance experience including prior line management experience
  • Experience with ICSR processing and second quality control of cases
  • Ability to create and maintain project-specific KPIs and optimize procedures
  • Strong written and verbal communication skills
  • Organizational skills with attention to detail and multitasking
  • Delegation, planning and time management skills
  • Technical skills relevant to pharmacovigilance operations (unspecified)
  • Teamwork and ability to act as team SME and support other SMEs
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The Company
HQ: London
535 Employees
Year Founded: 1997

What We Do

Founded in 1997, Ergomed is a global provider of high-quality services to the biopharmaceutical industry, spanning all phases of clinical trials, post-approval pharmacovigilance, and medical information. Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance (PV) solutions, integrated under the PrimeVigilance brand, and Ergomed Clinical Research, a complete, global Phase I-IV clinical development and trial management services with a strong heritage in the development of drugs in rare diseases and oncology. • 1,400+ highly qualified professionals • Global full-service CRO • 25+ years of experience • Therapeutic specialization in oncology • Strong expertise in rare disease trials • Robust clinical safety system • Choice of leading drug safety databases Our key services include: • Clinical Research Services • Pharmacovigilance • Medical Information • Regulatory • Medical Writing • Site Management • Study Physician Support • Biostatistics • Patient Study Support

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