8 Clinical Data And Biostatistics jobs in Stockholm.

Hiring now: Clinical Research Coordin @ Parexel, Clinical Trial Asst @ Iqvia, Global Trial Associate @ Johnson Jo, Sr Safety Data Sheet Spec @ Astrazenec.Explore more at jobswithgpt.com.

🔥 Skills

Clinical Trials (4) Data Management (4) Clinical Research (3) Remote (2) Regulatory (2) Biostatisticians (2) CRA (2) Biostatistics (2) Project Leader (2) Functional Service Provider (2)

📍 Locations

Stockholm (4) Solna (3) Södertälje (1)

Parexel

Skills & Focus: Clinical Research, Coordinator, Clinical Trials, Research Associate, Bilingual, Phlebotomist, Remote, Regulatory, Biostatisticians, Data Management
About the Company: Parexel helps biopharmaceutical companies and medical device manufacturers develop medical treatments and deliver them to market while ensuring patient safety.
Skills & Focus: Clinical Research, Clinical Trials, CRA, Biostatistics, Regulatory, Data Management, Project Leader, Functional Service Provider, Statistical Programming, Emerging Talent
About the Company: Parexel is a global biopharmaceutical services organization dedicated to providing expert solutions for regulatory and clinical development.
Type: Full-time
Skills & Focus: Clinical Research, Nurse, Clinical Trials, Registered Nurse, Remote, Associate, Project Leader, Biostatistics, FSP, Patient Safety

Iqvia

Skills & Focus: Clinical Research Associates, Trial Master File, administrative activities, clinical documents, compliance, project timelines, Case Report Forms, clinical monitoring, Good Clinical Practice, clinical 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: 3 years administrative support 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.

Johnson & Johnson

Skills & Focus: Clinical Trial, Project Management, Regulatory Compliance, Site Management, Investigator Meeting, Logistical Support, Pharmaceutical Development, Training, Data Management, Safety Updates
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: Must be graduating no more than 12 months prior to the target start date of July 2025.
Type: Hybrid

Iqvia

Skills & Focus: site monitoring, clinical research, Good Clinical Practice, protocol adherence, regulatory submissions, study management, data integrity, subject recruitment, documentation, communication skills
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: at least 2 years of year 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.

Astrazeneca

Skills & Focus: Safety Data Sheets, hazard communication, Global Chemical Regulations, CLP, GHS, regulatory queries, continuous improvement, project management, collaboration, pharmaceutical industry
About the Company: AstraZeneca, one of the world’s most forward-thinking and connected BioPharmaceutical companies, is committed to delivering life-changing medicines to patients…
Experience: Extensive expertise in Global Chemical Regulations, particularly CLP or GHS; Proven experience in the creation of Safety Data Sheets.