14 Clinical Operations Management jobs in Remote - Kingdom of Belgium.

Hiring now: Clinical Research Associa @ Iqvia, Site Care Partner Lead Cr @ Parexel, Experienced Clinical Rese @ Syneos Hea, Clinical Research Associa @ Precision .Explore more at jobswithgpt.com.

šŸ”„ Skills

Clinical Trials (4) monitoring (3) Good Clinical Practice (3) regulatory submissions (3) CRA (3) Functional Service Provider (3) Site Care Partner (3) project management (3) clinical studies (3) Clinical Research Associate (2)

šŸ“ Locations

Kingdom of Belgium (14)

Iqvia

Skills & Focus: Clinical Research Associate, site selection, monitoring, Good Clinical Practice, subject recruitment, regulatory submissions, data query resolutions, collaborating, organizational skills, 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: Experience in Pharma Industry, and/or Clinical Trials environment
Type: Full time
Benefits: Company car, mobile phone and attractive benefits packaging.

Parexel

Skills & Focus: Clinical Trials, CRA, Functional Service Provider, Site Care Partner, Biostatisticians, Data Managers, Project Leaders, Regulatory Consultants, Statistical Programmers, Emerging Talent Opportunities
About the Company: Parexel is a global biopharmaceutical services organization that offers solutions to expedite the development of safe and effective medical products.

Iqvia

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.
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.

Syneos Health

Skills & Focus: Clinical Research Associate, monitoring, Good Clinical Practice, Site Management, site qualification, informed consent, data integrity, clinical trial, regulatory compliance, patient safety
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Previous monitoring experience in Belgium
Type: Full-time
Skills & Focus: site contracts, negotiation, clinical study agreements, budget management, stakeholders, healthcare, clinical trials, CRO, French contracts, 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: Strong experience in a CRO/pharmaceutical industry and related clinical trial expertise.
Type: Full-time
Benefits: Career development and progression; supportive management; technical training; peer recognition and total rewards progr…
Site Activation Specialist Kingdom of Belgium
Skills & Focus: Site Activation, Clinical Trials, Submissions, Regulatory Affairs, Contract Negotiation, Project Management, Budget Management, Compliance, Team Collaboration, Problem Solving
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success by translating unique clinical, medi…
Experience: Detailed understanding of clinical trial process across Phases II-IV and ICH GCP. Ability to understand clinical protocols and associated study specifications.
Type: Full-time
Benefits: Supportive and engaged line management; technical and therapeutic area training; peer recognition; total rewards progra…

Parexel

Skills & Focus: Clinical Research, Site Management, Recruitment, Patient Safety, Study Activation, Stakeholder Collaboration, Data Management, Quality Assurance, Site Oversight, Project Management
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

Syneos Health

Skills & Focus: medical writing, clinical study protocols, IND submissions, FDA regulations, ICH guidelines, peer reviewer, clinical development, project management, review documents, 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: Bachelor of Science degree with relevant writing experience or Bachelor of Arts degree (Social Sciences, English or Communications, preferred) with relevant scientific and/or medical knowledge and expertise.
Type: Full-time
Benefits: Professional development, supportive management, and rewards programs.

Parexel

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

Precision For Medicine

Skills & Focus: clinical studies, monitoring, investigative sites, SOPs, ICH-GCP, onsite monitoring, regulatory submissions, protocol, oncology experience, domestic travel
About the Company: Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help th…
Experience: At least 2 years independent on site monitoring experience within the CRO or Pharmaceutical industry
Type: Full-time
Skills & Focus: clinical studies, protocol expertise, site monitoring, investigator meeting, regulatory submissions, ICH-GCP, oncology experience, travel commitment, quality outcomes, risk mitigation
About the Company: Precision for Medicine is not your typical CRO. We have brought together new technologies, expertise and operational scale to help the life sciences improve th…
Experience: At least 2 years independent site monitoring experience within the CRO or Pharmaceutical industry
Type: Full-time

Iqvia

Skills & Focus: clinical trial, operational planning, risk management, clinical studies, protocol development, GCP/ICH, stakeholder management, virtual teams, communications, negotiation
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: ≄ 4 years of recent involvement in clinical research or drug development
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.