
201 - 500 employees
đĽ Healthcare
đź Consulting
đŚ Logistics
Healthcare ⢠Consulting ⢠Logistics
Biomapas is a comprehensive outsourcing solution provider catering to the global life science sector. The company acts as a strategic partner for biopharmaceutical and medical device companies, offering extensive clinical research services worldwide. Biomapas covers the entire product lifecycle from regulatory compliance to pharmacovigilance and medical information. The company operates across various regions including Europe, CIS, EAEU, MENA, LATAM, and the US, ensuring high-quality, efficient, and cost-effective methodologies to deliver superior service and strategic advantages. With a focus on clinical trials, pharmacovigilance, and regulatory affairs, Biomapas is equipped to navigate complex regulatory environments and manage clinical trial data effectively, contributing to clients' commercial success.
Selected: đ Date Added.
đ 3 days ago
Senior Pharmacovigilance Specialist managing global and local pharmacovigilance systems. Ensuring regulatory compliance, PV project delivery, safety reporting, and audit readiness for life sciences partners.
đ 6 days ago
Senior Director leading global pharmacovigilance operations for a life science company. Overseeing centralized PV delivery, regulatory compliance, delivery hubs, outsourcing, and strategic client support.
đ 6 days ago
Pharmacovigilance Specialist serving as Local Safety Officer for DACH countries. Ensuring regulatory compliance, safety information processing, audits, literature monitoring, SOPs, and PV training.
đŠđŞ Germany â Remote
â° Full Time
đ˘ Junior
đĄ Mid-level
đŤđ¨âđ No degree required
đť Ghost score 10%
đŁď¸đŠđŞ German Required
đ August 20
Freelance Senior Start Up Associate managing clinical-trial start-up submissions in Greece under CTR via CTIS. Supporting site activation, regulatory communications, contracts, translations, and trial documentation.
đ August 18
Pharmacovigilance Associate supporting compliant drug-safety operations for DACH projects. Processing safety cases, monitoring literature, and preparing regulatory safety-report data remotely from Germany.
đŁď¸đŠđŞ German Required
đ August 18
Pharmacovigilance Specialist processing safety cases, medical reviews, and regulatory reports for pharmaceutical and CRO projects. Managing triage, quality checks, reconciliations, follow-ups, and safety-data line listings.
đ August 12
Freelance pharmacovigilance specialist supporting Icelandic safety operations and medical information. Managing safety reports, regulatory reviews, training, and client PV tasks remotely.
đŽđ¸ Iceland â Remote
âą Part Time
đ˘ Junior
đĄ Mid-level
⨠Support Specialist
đť Ghost score 10%
đŁď¸đŽđ¸ Icelandic Required
đ August 11
Senior clinical research leader overseeing multi-project portfolios for healthcare and CRO operations. Managing budgets, teams, sponsors, proposals, and business development across EU-based remote operations.
đ August 10
Clinical Project Manager overseeing compliant clinical trials for life sciences company. Coordinating teams, budgets, vendors, sponsors, and project plans across EU-based remote operations.
đ Lithuania, Poland, +4 more countries â Remote
â° Full Time
đĄ Mid-level
đ Senior
đĽ Clinical Operations
đť Ghost score 10%
đ July 10
Medical/Clinical Safety Specialist in Pharmacovigilance, ensuring compliance with regulations and safety reviews. Collaborating on safety data reporting and regulatory document preparation.
đđş Hungary â Remote
â° Full Time
đĄ Mid-level
đ Senior
⨠Clinical Specialist
đť Ghost score 19%
đ June 23