Last updated: 2025-05-22

19 Biopharmaceutical Leadership jobs in Remote - România.

Hiring now: Srprincipal Clinical Data @ Precision , Clinical Scientist @ Precision , Medical Dir Dermatology @ Parexel, Mgr Clinical Ops Sponsor @ Iqvia, Sr Clinical Research Asso @ Syneos Hea, Sr Feasibility Associatef @ Precisionm, Sr Clinical Data Mgrprinc @ Pfm.Explore more at at kaamvaam.com

🔥 Skills

Data Management (5) clinical research (5) programming (5) CDISC standards (5) EDC vendor (4) scripting (4) Project Management (3) data management (3) Clinical Research (3) EDC (3)

📍 Locations

România (19)

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 data, data quality, oncology standards, GCP/ICH compliance, electronic data capture (EDC), Data management, clinical operations, oncology clinical trials, risk management, team collaboration
About the Company: Precision for Medicine is focused on delivering customized scientific and operational support to the evolving life sciences landscape, enabling the acceleratio…
Experience: At least two (2) years in clinical operations and/or data management or related discipline in either the CRO or pharmaceutical industry and/or experience conducting oncology clinical research.
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.

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 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
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.

Parexel

Skills & Focus: Medical Monitoring, Consultative relationships, Drug Development, Client Engagement, Protocol Development, Safety Processing, Clinical Protocols, Team Collaboration, Medical Expertise, Regulatory Consulting
About the Company: Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe tr…
Experience: 5-10 years

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 trial, database development, quality control, data entry, SOPs, EDC, medical coding, stakeholders, leadership
Experience: Lead Data Manager for a Clinical Research Organisation or Pharmaceutical company
Type: Remote

Parexel

Skills & Focus: Procurement, Patient Recruitment, Remote, FSP, Clinical Trials, Global, Biopharmaceuticals, Project Management, Regulatory, Data Management
About the Company: Parexel is a global biopharmaceutical services company known for its clinical research and consulting services.
Skills & Focus: Medical Director, Dermatology, Clinical Research, Medical Sciences, Remote, Biopharma, Patient Care, Regulatory Compliance, Team Leadership, Data Management

Iqvia

Skills & Focus: clinical operations, clinical trials, management, GCP, ICH, leadership, performance assessment, resource allocation, training, quality management
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 4 years in a similar role with prior clinical trial 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: Clinical Research, Site Management, Regulatory Compliance, ICH-GCP, Pharmacovigilance, Data Integrity, Monitoring, Patient Recruitment, Clinical Trial, Auditing
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…

Iqvia

Skills & Focus: Regulatory Affairs, Russian market, Technical writing, Post-approval, Stakeholders, Regulatory submissions, Health Authority, Lifecycle management, Project management, Regulatory procedures
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.

Parexel

Skills & Focus: Regulatory Affairs, CMC, Pharmaceutical, Biologics, Quality Control, Submission Strategies, Market Expansions, Risk Management, Collaboration, Technical Documentation
About the Company: Parexel is a global biopharmaceutical services company that provides expertise in regulatory affairs, clinical research, and other related fields to help bring…
Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
Type: Remote
Benefits: Flexible work arrangements, supportive and inclusive environment, opportunities for career growth.

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

Iqvia

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.

Pfm

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