16 Biopharmaceutical Leadership jobs in Belgrade.

Hiring now: Regulatory Affairs Mgr Cm @ Parexel, Pv Officer @ Primevigil, Sr Site Activation Coordi @ Iqvia, Regulatory And Start Up S @ Precision , Regulatory Affairs Spec @ Viatris He, Site Activation Mgr @ Syneos Hea.Explore more at jobswithgpt.com.

🔥 Skills

Clinical Research (5) Data Management (5) Statistical Programming (4) Biostatistics (4) clinical trials (4) Clinical Trials (3) Functional Service Provider (3) communication (3) project management (3) Good Clinical Practice (3)

📍 Locations

Belgrade (16)

Parexel

Skills & Focus: Regulatory Affairs, CMC, Biologics, Project Leadership, Clinical Research, Data Management, Statistical Programming, Consulting, Medical Writing, Biostatistics
About the Company: Parexel is a global biopharmaceutical services organization that provides a range of services to enhance the clinical development of drugs and medical devices.
Type: Full-time
Skills & Focus: Clinical Trials, Data Management, Biostatistics, Clinical Research, FSP, CRA, Functional Service Provider, Oncology, Statistical Programming, Epidemiology
About the Company: Parexel helps clients accelerate the development and commercialization of innovative new therapies with expertise in regulatory consulting, clinical trials, an…
Skills & Focus: Clinical Research Associate, Biostatistics, Data Management, Statistical Programming, Functional Service Provider, Clinical Trials, Oncology, Remote Work, Life Sciences, Pharmaceuticals
About the Company: Parexel is a global biopharmaceutical services organization that provides comprehensive drug development and regulatory consulting services to the pharmaceutic…

Primevigilance

PV Officer Belgrade
Skills & Focus: case processing, pharmacovigilance, Individual Case Safety Reports, SAE/SUSAR Management, database outputs, mentoring, training, procedure optimization, clinical trials, regulatory compliance
About the Company: PrimeVigilance is a company specializing in pharmacovigilance and case processing services.
Experience: Several years in case processing

Iqvia

Skills & Focus: site activation, clinical research, experience, healthcare, interpersonal skills, communication, organization, project management, regulatory compliance, data management
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Minimum of 2 years of working experience; 1+ years in the health field or similar.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs.

Precision For Medicine

Skills & Focus: Regulatory, Start-Up, Clinical Trial, Submission, Compliance, Translation, Communication, Site Activation, Project Management, Negotiation
About the Company: Precision for Medicine is not your typical CRO. At Precision for Medicine, we have brought together new technologies, expertise and operational scale to help t…
Experience: 1 year or more as a Regulatory or SU specialist (or comparable role) in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies.

Viatris Healthcare D.O.O.

Skills & Focus: Regulatory Affairs, medicinal products, registration, variations, renewal application, local regulatory requirements, compliance, interpersonal skills, pharmaceutical industry, health authority
About the Company: At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolv…
Experience: 1-3 years at similar regulatory positions
Benefits: competitive salaries, benefits, and an inclusive environment

Syneos Health

Skills & Focus: Site Start-Up, project regulatory pathway, patient enrollment, project deliverables, risk identification, budget management, project milestones, clinical trial process, vendor management, communication skills
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Project management experience in a fast-paced environment.
Type: Hybrid

Iqvia

Skills & Focus: clinical studies, management, leadership, training, resource allocation, quality metrics, employee relations, professional development, clinical research, Good Clinical Practice
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Prior clinical trial experience including experience in a management/leadership capacity or equivalent combination of education, training and experience.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.
Skills & Focus: Clinical Research, Monitoring, GCP, ICH, Site Management, Regulatory, Data Submission, Subject Recruitment, Good Clinical Practice, Training
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Requires at least 1 years of on-site monitoring experience.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Syneos Health

Skills & Focus: clinical trials, project management, stakeholders, timelines, budgets, financial reports, communication, risk management, quality assurance, mentorship
About the Company: Syneos Health is a leading integrated biopharmaceutical solutions organization built to accelerate customer success.
Experience: Bachelor’s degree (or equivalent) in life sciences, medicine, pharmacy, nursing, project management or related field.
Skills & Focus: Project Management, Clinical Research, Good Clinical Practice, Regulatory Compliance, Financial Performance, Risk Mitigation, Study Launch, Team Leadership, Client Relationships, Data Management
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Experience managing Early Phase Global Studies
Type: Hybrid
Benefits: Career development, supportive management, technical training, total rewards program, commitment to diversity.
Skills & Focus: clinical study agreements, contract negotiations, budget management, site contracts lead, subject matter expert, stakeholder communication, training materials, process improvement, risk mitigation, clinical trial management
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Strong experience in a CRO/pharmaceutical industry and related clinical trial expertise (Study Coordinator, CRA, Pharmacy, Nursing, Healthcare Administration) or site start-up experience.
Type: Hybrid
Benefits: Career development and progression; supportive and engaged line management; technical and therapeutic area training; pe…

Primevigilance

Skills & Focus: pharmacovigilance, drug safety, Individual Case Safety Reports, data entry, quality review, compliance, clinical trials, post-marketing, report reconciliation, supervision
About the Company: PrimeVigilance is a company specializing in pharmacovigilance and drug safety services.
Experience: New graduates

Iqvia

Skills & Focus: site activation, clinical trials, healthcare, communication, project management, regulations, SOPs, feasibility, collaboration, documentation
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Minimum 2 years’ work experience; 1+ years in healthcare or similar
Type: Full-time