
1001 - 5000 employees
Founded 1997
đź Consulting
đĽ Healthcare
đŚ Logistics
Consulting ⢠Healthcare ⢠Logistics
ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.
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1001 - 5000 employees
Founded 1997
đź Consulting
đĽ Healthcare
đŚ Logistics
Consulting ⢠Healthcare ⢠Logistics
ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.
⢠Develop regulatory strategy based on regulatory requirements ⢠Drive regulatory and pharmacovigilance deliverables according to established plans ⢠Serve as liaison between regulatory and other functional areas, external partners, clients, authorities and consultants ⢠Act as Local Contact Person for Pharmacovigilance for the designated country ⢠Lead and functionally represent medium/high-complexity projects ⢠Coordinate and manage regulatory deliverables and ensure targets and procedures are met ⢠Develop strategy and manage project setup activities, including project management plans, joint operating procedures, POAs and core documents ⢠Provide strategic input and identify and address risks through preventive measures ⢠Resolve performance issues and delivery failures ⢠Maintain LCP CVs, job descriptions, training records, contact details and monthly reports ⢠Ensure LCP training assignments and compliance ⢠Monitor project tasks, time allocations, budgets and out-of-scope work ⢠Support proposal development, budgets and business development meetings ⢠Prepare client invoices and review or approve vendor project invoices ⢠Train, coach and mentor junior staff ⢠Maintain professional relationships with internal and external contacts ⢠Monitor regulatory legislative changes and maintain the regulatory intelligence database ⢠Support audit and inspection preparation ⢠Track LCP KPIs and prepare monthly summary reports ⢠Provide vendor performance feedback ⢠Contribute to company initiatives and SOPs, working practices and guidance
⢠Bachelor's Degree in Chemistry or Life Sciences, Nursing, or equivalent experience ⢠Strong experience within pharmaceutical or CRO industry or Regulatory body ⢠Good knowledge of ICH GCP and/or GVP and national regulations for territories of competency ⢠PV training and/or working experience and other educational or professional background as required locally ⢠Fluent in English, both written and verbal ⢠Proficient in the official language of the country in which they are based ⢠Good planning and organizational skills ⢠Strong interpersonal skills in a fast-paced, deadline oriented, and changing environment ⢠Good attention to detail
⢠Remote work availability ⢠Flexible work environment ⢠Growth opportunities ⢠Collaborative and supportive team culture ⢠Professional development through training, coaching and mentoring ⢠Global team and international exposure ⢠Belonging-focused workplace culture
Apply Nowđ June 30
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