Last updated: 2025-05-22

24 Clinical Operations Management jobs in Remote - Kingdom of Spain.

Hiring now: Site Care Partnersr Cra F @ Parexel, Clinical Research Associa @ Iqvia, Srprincipal Clinical Data @ Precision , Srprincipal Clinical Data @ Precision , Sr Dir Global Program Tea @ Astrazenec, Site Contracts Spec Sr Si @ Syneos Hea, Sr Feasibility Associatef @ Precisionm, Sr Clinical Data Mgrprinc @ Pfm.Explore more at at kaamvaam.com

šŸ”„ Skills

Clinical Trials (5) clinical research (5) Data Management (4) programming (4) CDISC standards (4) Quality Control (4) project management (4) clinical trials (4) Clinical Research (3) EDC vendor (3)

šŸ“ Locations

Kingdom of Spain (24)

Parexel

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

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 Medicine Group

Skills & Focus: clinical databases, EDC vendor, Data Management, Project Management, scripting, Object Oriented Programming, clinical research, programming, CDISC standards, database management
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 For Medicine

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.

Precision Medicine Group

Skills & Focus: Data Management, Clinical Trials, Database Development, Quality Control, Data Entry, Clinical Research, Project Management, Medical Coding, EDC, SOPs
Experience: Must have worked as a Lead Data Manager for a Clinical Research Organisation or Pharmaceutical company

Precision For Medicine

Skills & Focus: clinical database management, clinical data management, EDC, data management, clinical research, programming, scripting, CDISC standards, drug development, object-oriented programming
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…

Precision For Medicine

Skills & Focus: clinical studies, protocol expertise, investigator meetings, regulatory submissions, site visits, oncology, quality outcomes, risk mitigation, conflict resolution, study monitoring
About the Company: Precision for Medicine is a CRO passionate about cultivating culture with high CRA retention rates, allowing employees to have an influence and support from ma…
Experience: 2 years or more as a CRA in a CRO or pharmaceutical/biotech industry.

Precision Medicine Group

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

Astrazeneca

Skills & Focus: program ownership, global development strategy, oncology, drug development, clinical plans, project management, regulatory influence, collaborative, leadership, biopharmaceutical
About the Company: AstraZeneca is a global pharmaceutical company focused on the discovery, development, and commercialization of prescription medicines. They are committed to im…
Experience: Ten (10)+ years in drug development in pharmaceuticals, biopharmaceuticals, or biotechnology
Type: Full-time

Precision For Medicine

Skills & Focus: Regulatory strategy, Clinical trials, Regulatory submissions, Compliance, Project management, Regulatory Authorities, Drug development, Clinical Research Organisation, ICH, Quality initiatives
Experience: 5 to 7 years Regulatory experience

Iqvia

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 Companyā„¢, 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.

Parexel

Skills & Focus: Clinical Trials, Investigator Contracts, Spain, FSP, Remote Work, Biopharmaceutical, Regulatory Affairs, Patient Experience, Consulting, Medical Writing
About the Company: Parexel is a global biopharmaceutical services organization that provides solutions in consulting, clinical research, and commercialization. The company specia…
Type: Full-time

Syneos Health

Skills & Focus: clinical, contracts, clinical trial, management, negotiating, regulatory, startup, phases, assurance, compliance
About the Company: Syneos HealthĀ® is a fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success in clinical development, medical affai…
Experience: High level of contracts management experience

Iqvia

Skills & Focus: contract negotiation, clinical research, contract management, budget templates, proposal development, clinical trials, investigator grants, compliance, financial contracting, team collaboration
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: 2 to 5 years relevant sponsor or clinical research organization clinical site contracting 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 trials, project management, resource planning, risk management, financial management, communication, interpersonal skills, leadership, customer service, Microsoft Office
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: Five years related 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: Contract Management, Clinical Trials, Site Selection, Quality Control, Regulatory Compliance, Budget Management, Communication, Documentation, Problem-solving, Multi-tasking
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Associate’s Degree or equivalent combination of education and training preferred.
Type: Contract
Benefits: Career development and progression; supportive management; technical and therapeutic area training; peer recognition an…

Parexel

Senior Medical Writer Kingdom of Spain
Skills & Focus: Medical Writing, Clinical Research, Clinical Documents, Regulatory Submissions, Project Management, Client Liaison, Quality Control, Team Management, Mentoring, Scientific Writing
About the Company: Parexel is in the business of improving the world’s health by providing a suite of biopharmaceutical services that help clients transform scientific discoverie…
Benefits: competitive salary, bonus, and benefits package including holiday, pension, bonus

Precisionmedicinegroup

Skills & Focus: feasibility analysis, site identification, clinical protocols, study assumptions, client information, feasibility site outreach, post-award feasibility, patient advocacy groups, enrollment modeling, clinical trial
Experience: 5 years

Pfm

Skills & Focus: clinical, data, management, database, protocol, CRF, UAT, bioinformatics, regulatory, healthcare
Skills & Focus: clinical, data, management, database, protocol, CRF, UAT, bioinformatics, regulatory, healthcare
Skills & Focus: feasibility analysis, site identification, clinical protocols, study assumptions, epidemiology analysis, study delivery, study feasibility, site outreach, post-award feasibility, data analysis
Experience: At least 5 years

Parexel

Skills & Focus: Regulatory Affairs, project management, clinical trials, client relationships, compliance, project execution, budget management, resource planning, cross-functional teams, therapeutic areas
About the Company: Parexel is a global biopharmaceutical services organization that provides a broad range of expertise to support the development and market access of innovative…
Experience: extensive experience in Regulatory Affairs, PMP or equivalent certification preferred

Pfm

Skills & Focus: feasibility analysis, site identification, clinical trials, pre-award, post-award, site outreach, feasibility projects, biotech, pharma, biopharmaceutical
Experience: 5 years