14 Clinical Operations Management jobs in Remote - Italian Republic.

Hiring now: Risk Surveillance Lead Fs @ Parexel, Clinical Research Associa @ Syneos Hea, Clinical Research Associa @ Iqvia, Regulatory And Start Up S @ Precision .Explore more at jobswithgpt.com.

šŸ”„ Skills

Clinical Research (5) Data Management (3) Monitoring (3) Good Clinical Practice (3) FSP (2) Trial Master File (2) Regulatory Compliance (2) clinical trial management (2) risk mitigation (2) Regulatory (2)

šŸ“ Locations

Italian Republic (14)

Parexel

Skills & Focus: Project Leadership, Risk Surveillance, FSP, Clinical Research, Project Plans, SOPs, ICH, GCP, Compliance, Budget

Syneos Health

Skills & Focus: Clinical Research, Project Planning, Protocol Documentation, Trial Master File, Study Coordination, Good Clinical Practices, Patient Safety, Quality Control, Regulatory Documentation, Data Management
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: A minimum of 1 year experience in clinical research required, preferably in coordination of clinical research projects.
Type: Part, Full time

Iqvia

Skills & Focus: Clinical Research, Site Selection, Monitoring, Data Management, Regulatory Compliance, Pharma Industry, Recruitment Plan, Quality Evaluation, Good Clinical Practice, International Conference on Harmonization
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: Experience in Pharma Industry, and/or Clinical Trials environment
Type: Full time
Benefits: Company car, mobile phone and attractive benefits package
Skills & Focus: clinical trial management, study management team, project planning, risk mitigation, compliance, stakeholder management, data collection, vendor oversight, document management, training materials
About the Company: IQVIA is working to create a healthier world through diverse expertise, innovation, and powerful capabilities in the healthcare sector.
Experience: 6-8 years clinical trial management experience in the pharmaceutical industry or CRO.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Precision For Medicine

Skills & Focus: Regulatory, Clinical Trial, Site Activation, CA/EC submissions, Project Management, Essential Documents, Informed Consent, Translation, Audit/Inspection, Communication
About the Company: Precision Medicine Group is an organization serving clients that are researching ground breaking cancer therapies.
Experience: 1 year or more as a Regulatory or SU specialist (or comparable role) in either a CRO or pharmaceutical/biotech industry

Parexel

Skills & Focus: Remote, FSP, Vendor Start Up Manager, Management, Procurement, Clinical, Research, Development, Service Provider, Biopharmaceutical
About the Company: Parexel is a global biopharmaceutical services provider, partnering with clients to accelerate the development of innovative new medicines.

Syneos Health

Skills & Focus: clinical monitoring, site management, patient safety, GCP compliance, data integrity, risk management, protocol execution, clinical trial management, project milestones, investigator payments
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Experience in Gene therapy or OGM studies is strictly required.
Type: fixed term assignment
Benefits: Career development and progression; supportive and engaged line management; technical and therapeutic area training; pe…
Sr Site Contracts Lead Italian Republic
Skills & Focus: site contracts, clinical trial agreements, negotiations, consultation, contract execution, budget management, stakeholder communication, training, mentorship, risk mitigation
About the Company: Syneos HealthĀ® 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.

Precision For Medicine

Skills & Focus: Regulatory, site activation, Clinical Trial Application, submissions, approvals, Feasibility, communication, contract negotiations, audit readiness, local regulations
About the Company: Precision Medicine Group is an organization serving clients that are researching groundbreaking cancer therapies.
Experience: 1 year or more as a Regulatory or SU specialist (or comparable role)

Syneos Health

Skills & Focus: Clinical Research, Monitoring, Regulatory Compliance, Good Clinical Practice, Data Integrity, Site Management, Risk Assessment, Training, Audit Preparation, Project Management
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience.

Parexel

Skills & Focus: Clinical Trials, Functional Service Provider, CRA, Site Care Partner, Remote, Biostatisticians, Health Research, Regulatory Consultants, Project Leaders, Statistical Programmers
About the Company: Parexel is a leading global biopharmaceutical services organization that offers a broad range of services, including biostatistics, clinical trials, site manag…
Type: Remote

Iqvia

Study Start Up Lead Italian Republic
Skills & Focus: site activation, clinical trials, regulatory compliance, project management, biotechnology, clinical practice guidelines, study initiation, budget planning, contract negotiation, regulatory intelligence
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: 7 years relevant 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, Site Management, Monitoring, Good Clinical Practice, Regulatory Requirements, Study Protocol, Recruitment, Data Management, Trial Master File, 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 3 years prior clinical experience preferred.
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, CRA, Functional Service Provider, Site Care Partner