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Senior Clinical Research Associate
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Madrid, Madrid, España Worldwide Clinical Trials A tiempo completoClinical Trials Career Opportunities **About Us** Worldwide Clinical Trials is a leading global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications from discovery to reality. **Our Mission** We are united in cause with our customers to...
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Senior Clinical Research Associate
hace 2 semanas
Madrid Centro, Madrid, España Worldwide Clinical Trials A tiempo completoAbout the RoleWorldwide Clinical Trials is seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a vital role in ensuring the quality and excellence of our clinical research programs.Key ResponsibilitiesConduct site qualifications, initiation, interim monitoring, site management, and study...
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Senior Clinical Research Associate
hace 2 semanas
Madrid Centro, Madrid, España Worldwide Clinical Trials A tiempo completoAbout the RoleWorldwide Clinical Trials is seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a vital role in ensuring the quality and excellence of our clinical research programs.Key ResponsibilitiesConduct site qualifications, initiation, interim monitoring, site management, and study...
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Senior Clinical Research Associate
hace 2 semanas
Madrid, Madrid, España Worldwide Clinical Trials A tiempo completoAbout the RoleAt Worldwide Clinical Trials, we are committed to advancing new medications and improving the lives of patients through innovative therapies. As a Clinical Research Associate, you will play a vital role in ensuring the quality and excellence of our clinical research programs.Key ResponsibilitiesConduct site qualifications, initiation, interim...
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Senior Clinical Research Associate
hace 2 semanas
Madrid, Madrid, España Worldwide Clinical Trials A tiempo completoAbout the RoleAt Worldwide Clinical Trials, we are committed to advancing new medications and improving the lives of patients through innovative therapies. As a Clinical Research Associate, you will play a vital role in ensuring the quality and excellence of our clinical research programs.Key ResponsibilitiesConduct site qualifications, initiation, interim...
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Senior Clinical Research Associate
hace 3 semanas
Madrid, Madrid, España Worldwide Clinical Trials A tiempo completoJob SummaryWe are seeking a highly skilled and experienced Clinical Research Associate to join our team at Worldwide Clinical Trials. As a Clinical Research Associate, you will play a vital role in ensuring the quality and excellence of our clinical research programs.Key ResponsibilitiesConduct all types of visits, including site qualifications, initiation,...
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Senior Clinical Research Associate
hace 3 semanas
Madrid, Madrid, España Worldwide Clinical Trials A tiempo completoJob SummaryWe are seeking a highly skilled and experienced Clinical Research Associate to join our team at Worldwide Clinical Trials. As a Clinical Research Associate, you will play a vital role in ensuring the quality and excellence of our clinical research programs.Key ResponsibilitiesConduct all types of visits, including site qualifications, initiation,...
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Senior Clinical Research Associate
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Madrid, Madrid, España Worldwide Clinical Trials A tiempo completoAbout the RoleAs a Senior Clinical Research Associate - Clinical Operations Site Management at Worldwide Clinical Trials, you will play a vital role in ensuring the execution of our clinical research programs with the highest quality and excellence our sponsors expect.Key ResponsibilitiesConduct all types of visits, including site qualifications, initiation,...
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Senior Clinical Research Associate
hace 3 semanas
Madrid, Madrid, España Worldwide Clinical Trials A tiempo completoAbout the RoleAs a Senior Clinical Research Associate - Clinical Operations Site Management at Worldwide Clinical Trials, you will play a vital role in ensuring the execution of our clinical research programs with the highest quality and excellence our sponsors expect.Key ResponsibilitiesConduct all types of visits, including site qualifications, initiation,...
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Senior Clinical Research Associate
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Madrid, Madrid, España Worldwide Clinical Trials A tiempo completoCompany OverviewWorldwide Clinical Trials is a leading global contract research organization (CRO) that partners with biotechnology and pharmaceutical companies to create customized solutions that advance new medications from discovery to reality.Our MissionWe are united in our mission to improve the lives of patients through new and innovative therapies....
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Senior Clinical Research Associate
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Madrid, Madrid, España Worldwide Clinical Trials A tiempo completoCompany OverviewWorldwide Clinical Trials is a leading global contract research organization (CRO) that partners with biotechnology and pharmaceutical companies to create customized solutions that advance new medications from discovery to reality.Our MissionWe are united in our mission to improve the lives of patients through new and innovative therapies....
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Clinical Research Associate
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Madrid, Madrid, España Worldwide Clinical Trials A tiempo completo{"title": "Clinical Research Associate - Site Management", "content": "Role OverviewAs a Clinical Research Associate - Site Management, you will play a vital role in ensuring the quality and excellence of our clinical research programs. You will be responsible for conducting site qualifications, initiation, interim monitoring, site management, and study...
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Clinical Research Associate
hace 2 semanas
Madrid, Madrid, España Worldwide Clinical Trials A tiempo completo{"title": "Clinical Research Associate - Site Management", "content": "Role OverviewAs a Clinical Research Associate - Site Management, you will play a vital role in ensuring the quality and excellence of our clinical research programs. You will be responsible for conducting site qualifications, initiation, interim monitoring, site management, and study...
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Senior Clinical Research Associate
hace 3 semanas
Madrid, Madrid, España Worldwide Clinical Trials A tiempo completoAbout the RoleWe are seeking a highly skilled Clinical Research Associate to join our Clinical Operations team at Worldwide Clinical Trials. As a Clinical Research Associate, you will play a vital role in ensuring the quality and excellence of our clinical research programs.Key ResponsibilitiesConduct site qualifications, initiation, interim monitoring, site...
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Senior Clinical Research Associate
hace 3 semanas
Madrid, Madrid, España Worldwide Clinical Trials A tiempo completoAbout the RoleWe are seeking a highly skilled Clinical Research Associate to join our Clinical Operations team at Worldwide Clinical Trials. As a Clinical Research Associate, you will play a vital role in ensuring the quality and excellence of our clinical research programs.Key ResponsibilitiesConduct site qualifications, initiation, interim monitoring, site...
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Senior Clinical Research Associate
hace 2 semanas
Madrid, Madrid, España Worldwide Clinical Trials A tiempo completoAbout the RoleWe are seeking a highly skilled Clinical Research Associate to join our team at Worldwide Clinical Trials. As a key member of our Clinical Operations team, you will play a vital role in ensuring the successful execution of our clinical research programs.Key ResponsibilitiesConduct site qualifications, initiation, interim monitoring, site...
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Senior Clinical Research Associate
hace 2 semanas
Madrid, Madrid, España Worldwide Clinical Trials A tiempo completoAbout the RoleWe are seeking a highly skilled Clinical Research Associate to join our team at Worldwide Clinical Trials. As a key member of our Clinical Operations team, you will play a vital role in ensuring the successful execution of our clinical research programs.Key ResponsibilitiesConduct site qualifications, initiation, interim monitoring, site...
Senior Clinical Research Associate
hace 3 meses
.Who we areWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality.Anchored in our company's scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.Our talented team of 3,000+ professionals spans 60+ countries.We are united in cause with our customers to improve the lives of patients through new and innovative therapies.Why WorldwideWe believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join usWhat Clinical Operations Site Management does at WorldwideClinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role on every clinical trial. All CROs will promise you growth, opportunity and maybe even a challenge. But we offer more than that. We offer an uncommon experience – one you can't get anywhere else, with a team unlike anyone else.What you will do- Conduct all types of visits – site qualifications, initiation, interim monitoring, site management and study close-out visits- Review study subject safety information and informed consent and conduct source document verification for compliance, patient safety, and veracity of data- Actively participate in study team and investigator meetings- Compile and ensure completeness of regulatory documents and ethical submission documentation and review study subject safety information and informed consent and study material (e.G. CRFs, manuals)What you will bring to the role- Excellent interpersonal, oral, and written communication skills in English and local language- Superior organizational skills with attention to details- Broad understanding of clinical research principles and process- Proficiency in Microsoft Office, CTMS and EDC SystemsYour background- Four-year college curriculum in life sciences, OR- Two-year college curriculum or equivalent education / training (nursing degree or equivalent life science degree) and one year experience with clinical research (e.G. study coordinator, CTA, etc
