19 Clinical Operations Management jobs in Remote - Serbia.

Hiring now: Risk Surveillance Lead Fs @ Parexel, Site Contracts Spec @ Syneos Hea, Srprincipal Clinical Data @ Precision , Sr Clinical Data Mgrprinc @ Precision , Regulatory And Start Up D @ Iqvia.Explore more at jobswithgpt.com.

🔥 Skills

clinical research (4) Data Management (4) Clinical Trials (4) Clinical Research (3) clinical trials (3) project management (3) EDC vendor (3) programming (3) clinical trial (3) risk management (3)

📍 Locations

Serbia (19)

Parexel

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

Syneos Health

Skills & Focus: contracts management, clinical trials, negotiation, budgets, clinical development, quality control, project management, contract templates, site-specific contracts, vendor management
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success by translating unique clinical, medi…
Experience: Moderate contracts management experience that includes experience in a contract research organization or pharmaceutical industry
Type: Full-time

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, CRF Specifications, Data Management Documentation, Training, Medical Coding, SOPs, Clinical Study Protocol
Experience: Lead Data Manager for a Clinical Research Organisation or Pharmaceutical company
Type: Remote

Syneos Health

Skills & Focus: Clinical Regulatory Affairs, Oncology, Site Start-Up, project regulatory pathway, patient enrollment, project deliverables, quality standards, clinical trial agreements, project budgets, regulatory activities
About the Company: Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medica…
Experience: Minimum 6 years CRO industry experience and/or a minimum 5 years’ experience working in a SSU or clinical trial environment.
Type: Full-time
Benefits: Career development and progression; total rewards program.

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

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: contract management, clinical trials, budget preparation, negotiation skills, project management, clinical development process, vendor management, communication skills, team orientation, organizational skills
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…

Parexel

Skills & Focus: Investigator Payment, clinical trial, payment setup, project team, risk management, budgeting, audits/inspections, payment strategy, timely payments, data analysis
About the Company: Parexel is in the business of improving the world’s health by providing a suite of biopharmaceutical services that help clients across the globe transform scie…
Type: Remote
Benefits: competitive base salary and a benefits package including holiday as well as other benefits

Syneos Health

Skills & Focus: project management, clinical trial, regulatory documents, team communication, administrative support, quality assurance, data queries, audits, Good Clinical Practice, organization
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.

Precision For Medicine

Skills & Focus: Drug Safety, Pharmacovigilance, Clinical Trials, Signal Detection, Risk Management, Safety Reporting, Safety Data Management, Adverse Events, Regulatory Compliance, Medical Review
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level usi…
Experience: minimum of 7 years in Drug Safety related activities in pharma/biotech
Type: Remote
Skills & Focus: clinical databases, EDC vendor, Data Management, Project Management, programming, scripting, Microsoft Office, clinical research, data management, leadership
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.
Skills & Focus: pharmacovigilance, safety reporting, clinical support, risk management, signal detection, safety data management, adverse events, compliance, drug safety, clinical trials
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level usi…
Experience: Minimum of 7 years in Drug Safety related activities in pharma/biotech.

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.

Precision Medicine Group

Skills & Focus: Drug Safety, Pharmacovigilance, regulatory requirements, medical review, risk management, safety reporting, clinical trial, safety data analysis, signal detection, Good Clinical Practice
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level usi…
Experience: 7 years
Type: Full-time

Parexel

Skills & Focus: Procurement, Patient Recruitment, Remote, Functional Service Provider, Clinical Trials, Vendor Management, Project Management, Regulatory Compliance, Stakeholder Engagement, Contract Negotiation

Iqvia

Skills & Focus: Regulatory Affairs, Technical Writing, Project Management, Budget Management, Russian Language, Post Approval Regulatory, Lifecycle Management, Clinical Research, Regulatory Procedures, Client Relationships
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 throug…
Experience: At least 5 years relevant experience in lifecycle management regulatory affairs for Russian market
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, Trial Master File, administrative support, CRAs, clinical documentation, GCP, ICH guidelines, regulatory requirement, data flow, Case Report Forms
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: 3-4 years administrative support experience. Minimum one year clinical research 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.