19 Clinical Data And Biostatistics jobs in Remote - Kingdom of Spain.

Hiring now: Study Ops Mgr Spain Fsp @ Parexel, Principal Clinical Scient @ Precision , Clinical Research Associa @ Iqvia, Srprincipal Clinical Data @ Precision , Medical Writer Ii Lay Sum @ Syneos Hea.Explore more at jobswithgpt.com.

🔥 Skills

Clinical Trials (8) CRA (4) clinical research (4) programming (4) CDISC standards (4) Data Management (4) Clinical Research (3) data management (3) EDC vendor (3) Database Development (3)

📍 Locations

Kingdom of Spain (19)

Parexel

Skills & Focus: Clinical Research, FSP, Remote, CRA, Biostatisticians, Clinical Trials, Project Leaders, Data Managers, Regulatory Consultants, Statistical Programmers

Precision For Medicine

Skills & Focus: Clinical Trials, Oncology Standards, Data Cleaning, Clinical Research, Electronic Data Capture (EDC), Data Review, Medical Monitor, Cross-functional Communication, User Acceptance Testing (UAT), Clinical Data Review Guidelines
About the Company: Precision Medicine Group, LLC is an Equal Opportunity Employer focused on the life sciences and healthcare sectors.
Experience: Minimum of 8 years of clinical research experience; Minimum of 1 year of leadership experience
Type: Remote
Skills & Focus: clinical database management, clinical research, data management, EDC vendor, programming, scripting, CDISC standards, object-oriented programming, clinical research tasks, biomarkers
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…
Experience: Experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline; Medidata Rave EDC Certified Study Builder; Rave API integration experience.

Iqvia

Skills & Focus: Clinical Research, site selection, monitoring, Good Clinical Practice, International Conference on Harmonization, regulatory submissions, data query resolutions, effective working relationships, problem-solving skills, therapeutic knowledge
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Experience: Experience in Pharma Industry, and/or Clinical Trials environment
Type: Full time
Benefits: Resources that promote your career growth, flexible work schedules, excellent working environment

Precision For Medicine

Skills & Focus: Clinical Database Manager, clinical data management, EDC vendor, Medidata Rave, Rave API, programming, scripting, CDISC standards, drug development, clinical research
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…
Experience: Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline

Precision Medicine Group

Skills & Focus: clinical databases, Data Management, EDC vendor, operational training, programming, clinical research, Object Oriented Programming, scripting language, CDISC standards, database management systems
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…
Skills & Focus: Data Management, Clinical Trials, Database Development, Quality Control, Data Entry, Clinical Protocol, Training, Documentation, Medical Coding, SOP Development
Experience: Bachelors and/or a combination of related experience; Must have worked as a Lead Data Manager for a Clinical Research Organisation or Pharmaceutical company

Precision For Medicine

Skills & Focus: Principal Clinical Scientist, oncology, clinical trials, data management, data cleaning, electronic data capture systems, clinical research experience, scientific input, user acceptance testing, cross-functional communication
About the Company: Precision Medicine Group is dedicated to enabling innovation in the healthcare sector, particularly in clinical trials focusing on oncology and other medical d…
Experience: Minimum of 8 years of clinical research experience; Minimum of 1 year of leadership experience
Type: Remote

Iqvia

Skills & Focus: clinical trials, study management, Vendor Management, project management, patient outcomes, data management, healthcare intelligence, protocol development, regulatory documents, 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 industri…
Experience: 2-5 years of experience in managing late phase clinical trials at global level
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 Data Management, project management, Good Clinical Practices, customer negotiations, data management products, quality deliverables, milestone deliverables, issue escalation, data management plan, subject matter expert
About the Company: IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through…
Experience: 5+ years direct Clinical Data Management experience in CRO or pharmaceuticals industry, including 3+ years as a CDM project lead
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: medical writing, regulatory writing, clinical study reports, lay summaries, plain language summaries, patient information, quality checks, document preparation, health literacy, clinical research
About the Company: Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
Experience: Minimum 2 years of regulatory writing experience.

Precision Medicine Group

Skills & Focus: Clinical Data Management, Database Development, Data Quality Control, Clinical Trials, Regulatory Compliance, Project Management, Data Entry Guidelines, Medical Coding, SOP Development, Stakeholder Communication
Experience: Must have worked as a Lead Data Manager for a Clinical Research Organisation or Pharmaceutical company
Type: Remote

Syneos Health

Skills & Focus: quality control, clinical documents, copyedit, proofread, format, data content, clinical study protocols, submission standards, attention to detail, EDMS
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Must be performing at Senior level.
Benefits: We are passionate about developing our people, through career development and progression; supportive and engaged line …

Precision Medicine Group

Skills & Focus: Clinical Data Management, Oncology, Orphan Drug, Database Development, Quality Control, CRF specifications, SOPs, Data Entry Guidelines, CDISC standards, Medical Coding
About the Company: Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation,…
Experience: 8+ years’ experience with strong Oncology and/or Orphan Drug therapeutic experience
Type: Full-time

Parexel

Skills & Focus: Clinical Trials, CRA, Functional Service Provider, Site Care Partner

Iqvia

Skills & Focus: Statistics, Psychometrics, Clinical Trials, Data Analysis, Statistical Methodology, Programming in SAS, Programming in R, Psychometric Instruments, Patient Outcomes, Consulting
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Parexel

Skills & Focus: Functional Service Provider, Clinical Trials, Site Care Partner, CRA, Clinical Research Associate, Project Leader, Biostatistics, Regulatory Affairs, Data Management, Statistical Programming
About the Company: Parexel helps accelerate the development of new medical treatments and therapies.
Type: Full-time

Syneos Health

Skills & Focus: biostatistics, clinical trials, HEOR, HTA, statistical design, analysis, regulatory submissions, programming, CSR, SAS
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 with late phase studies working within HEOR and/or HTA is required.
Benefits: Career development and progression; supportive and engaged line management; technical and therapeutic area training; pe…

Parexel

Site Care Partner I Kingdom of Spain
Skills & Focus: Clinical Trials, Functional Service Provider, CRA, Site Care Partner, Biostatistics, Statistical Programming, Data Management, Regulatory Consulting, Project Leadership, Emerging Talent
About the Company: Parexel is a global biopharmaceutical services company that provides expertise in clinical research and regulatory consulting.