Proposals Manager - Pharmacovigilance

Reposted 2 Days Ago
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Hiring Remotely in Zagreb, HRV
In-Office or Remote
Senior level
Biotech • Pharmaceutical
The Role
Lead and coordinate development of client-focused pharmacovigilance proposals and budgets. Gather and QC stakeholder inputs, support contract negotiation and change orders, and streamline proposal processes. Train and mentor junior staff, participate in RFP triage and special projects, and ensure senior management engagement on key opportunities.
Summary Generated by Built In
Company Description

PrimeVigilance (part of Ergomed Group) is 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

Responsibilities include:

  • Strategically support and lead the development of proposals, including support strategy development and leading TCs
  • Ensure proposal input obtained from a variety of stakeholders, typically involving contributions from sales, marketing, operational teams, finance, legal and top management
  • QC and sense check of stakeholder feedback
  • Ensure high quality client-focused proposals, budgets and client grids are delivered for new business opportunities
  • Attend department meetings including global RFP Triage, P&C internal meetings, and other adhoc calls
  • Support and Participate at Proposals training which includes the onboarding of new staff as well as ongoing training of existing staff as well as personnel outside the P&C team
  • Support in activities related to coordination, development, negotiation and execution of client contracts and change orders for key accounts and key opportunities
  • Support the development of Standardized procedures on a departmental level, and support in streamlining processes on proposal preparation and efficient turnaround timelines
  • Support the development of junior staff by organizing  lessons learned and continued education programs to optimize team performance and growth
  • Support process improvement initiatives that result in the development of costs and proposals of the highest accuracy and effectiveness
  • Ensure Senior Management are appropriately involved in QC and contribution to Key Opportunities and their strategies are effectively communicated to the client
  • Ensure continuous departmental process improvements and participate in special projects periodically assigned, in addition to day-to-day duties

Qualifications

  • Proven experience developing proposals and managing budgets within the Clinical Research Organization (CRO) industry.
  • Background in Pharmacovigilance (Safety Services) or with PV providers is a plus

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. 

#LI-remote

Skills Required

  • Proven experience developing proposals and managing budgets within the Clinical Research Organization (CRO) industry
  • Background in Pharmacovigilance (Safety Services) or with PV providers
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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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