Empleos actuales relacionados con Global Study Associate - Barcelona, Barcelona - AstraZeneca
-
Study Start Up Associate
hace 2 semanas
Barcelona, Barcelona, España Sin nombre A tiempo completoAbout the RoleWe are seeking a highly skilled and experienced Study Start Up Associate to join our team at Sin nombre. As a key member of our Study Start Up Team, you will play a critical role in ensuring that physicians at our research sites are prepared to start clinical trials.Key ResponsibilitiesContract Review and Negotiation: Review and negotiate...
-
Study Start Up Associate
hace 2 semanas
Barcelona, Barcelona, España Sin nombre A tiempo completoAbout the RoleWe are seeking a highly skilled and experienced Study Start Up Associate to join our team at Sin nombre. As a key member of our Study Start Up Team, you will play a critical role in ensuring that physicians at our research sites are prepared to start clinical trials.Key ResponsibilitiesContract Review and Negotiation: Review and negotiate...
-
Study Start Up Associate
hace 2 semanas
Barcelona, Barcelona, España Sin Nombre A tiempo completoAbout the RoleWe are seeking a highly skilled and experienced Study Start Up Associate to join our team at Sin Nombre. As a key member of our Study Start Up Team, you will play a critical role in ensuring that physicians at our research sites are prepared to start clinical trials.Key ResponsibilitiesReview and negotiate clinical site investigator contracts...
-
Study Start Up Associate
hace 2 semanas
Barcelona, Barcelona, España Sin Nombre A tiempo completoAbout the RoleWe are seeking a highly skilled and experienced Study Start Up Associate to join our team at Sin Nombre. As a key member of our Study Start Up Team, you will play a critical role in ensuring that physicians at our research sites are prepared to start clinical trials.Key ResponsibilitiesReview and negotiate clinical site investigator contracts...
-
Clinical Research Associate
hace 2 semanas
Barcelona, Barcelona, España Mygwork A tiempo completoJob SummaryWe are seeking a highly motivated and organized Clinical Research Associate to join our team at ICON plc. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials by ensuring the smooth execution of study protocols, maintaining accurate records, and providing exceptional support to our clients.Key...
-
Clinical Research Associate
hace 2 semanas
Barcelona, Barcelona, España Mygwork A tiempo completoJob SummaryWe are seeking a highly motivated and organized Clinical Research Associate to join our team at ICON plc. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials by ensuring the smooth execution of study protocols, maintaining accurate records, and providing exceptional support to our clients.Key...
-
Senior Clinical Research Associate
hace 2 semanas
Barcelona, Barcelona, España IQVIA A tiempo completoAbout the RoleWe are seeking a highly skilled and experienced Clinical Research Associate to join our team at IQVIA. As a Sponsor-Dedicated CRA, you will be responsible for performing site selection, initiation, monitoring, and close-out visits, as well as supporting the development of a subject recruitment plan.Key ResponsibilitiesSite Selection and...
-
Senior Clinical Research Associate
hace 2 semanas
Barcelona, Barcelona, España IQVIA A tiempo completoAbout the RoleWe are seeking a highly skilled and experienced Clinical Research Associate to join our team at IQVIA. As a Sponsor-Dedicated CRA, you will be responsible for performing site selection, initiation, monitoring, and close-out visits, as well as supporting the development of a subject recruitment plan.Key ResponsibilitiesSite Selection and...
-
Associate Director, Development Asset Quality
hace 5 días
Barcelona, Barcelona, España Importante Empresa A tiempo completoJob Title: Associate Director, Development Asset QualityAt Importante Empresa, we are seeking an experienced Associate Director, Development Asset Quality to join our team. As a key member of our Development Quality Team, you will drive Quality Culture with Development, Regulatory, and Safety stakeholders through learning, embedding a quality mindset, and...
-
Associate Director, Development Asset Quality
hace 6 días
Barcelona, Barcelona, España Importante Empresa A tiempo completoJob Title: Associate Director, Development Asset QualityAt Importante Empresa, we are seeking an experienced Associate Director, Development Asset Quality to join our team. As a key member of our Development Quality Team, you will drive Quality Culture with Development, Regulatory, and Safety stakeholders through learning, embedding a quality mindset, and...
-
Global Product Associate Director
hace 6 días
Barcelona, Barcelona, España Almirall A tiempo completo{"title": "Global Product Associate Director", "description": "Key ResponsibilitiesWe are seeking a highly skilled Global Product Associate Director to join our dynamic Global Marketing team based in Barcelona. As a key member of our team, you will be responsible for supporting the Global Senior Director for the brand in the development of the Global Brand...
-
Global Product Associate Director
hace 6 días
Barcelona, Barcelona, España Almirall A tiempo completo{"title": "Global Product Associate Director", "description": "Key ResponsibilitiesWe are seeking a highly skilled Global Product Associate Director to join our dynamic Global Marketing team based in Barcelona. As a key member of our team, you will be responsible for supporting the Global Senior Director for the brand in the development of the Global Brand...
-
Global Health Economics Director
hace 6 días
Barcelona, Barcelona, España Ellie Mental Health - 077 A tiempo completoJob SummaryWe are seeking an experienced Associate Director to lead our Global Health Economics & Outcomes Research (GHEOR) Analytics team. The successful candidate will develop and implement HEOR Analytics strategy, including real-world study design and conduct, identification of data sources, and execution of publication plans.Key ResponsibilitiesDesign...
-
Global Health Economics Director
hace 6 días
Barcelona, Barcelona, España Ellie Mental Health - 077 A tiempo completoJob SummaryWe are seeking an experienced Associate Director to lead our Global Health Economics & Outcomes Research (GHEOR) Analytics team. The successful candidate will develop and implement HEOR Analytics strategy, including real-world study design and conduct, identification of data sources, and execution of publication plans.Key ResponsibilitiesDesign...
-
Associate, Scorecards, Risk Solutions
hace 2 semanas
Barcelona, Barcelona, España Global A tiempo completoAbout the RoleWe are seeking a highly skilled Risk Management Associate to join our team in Madrid, Spain. As a key member of our Scorecards business, you will play a critical role in delivering credit risk management services to clients across Europe.The TeamOur Scorecards team is a high-performing group of professionals who are passionate about delivering...
-
Associate, Scorecards, Risk Solutions
hace 2 semanas
Barcelona, Barcelona, España Global A tiempo completoAbout the RoleWe are seeking a highly skilled Risk Management Associate to join our team in Madrid, Spain. As a key member of our Scorecards business, you will play a critical role in delivering credit risk management services to clients across Europe.The TeamOur Scorecards team is a high-performing group of professionals who are passionate about delivering...
-
Clinical Research Associate Regional Monitoring
hace 2 semanas
Barcelona, Barcelona, España Resourcing Life Science A tiempo completoJob OverviewWe are seeking a skilled Clinical Research Associate to join our team at Resourcing Life Science. As a Regional Monitoring Clinical Research Associate, you will be responsible for monitoring clinical studies in phases II-III, ensuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.Key...
-
Clinical Research Associate Regional Monitoring
hace 2 semanas
Barcelona, Barcelona, España Resourcing Life Science A tiempo completoJob OverviewWe are seeking a skilled Clinical Research Associate to join our team at Resourcing Life Science. As a Regional Monitoring Clinical Research Associate, you will be responsible for monitoring clinical studies in phases II-III, ensuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.Key...
-
Clinical Research Associate
hace 2 semanas
Barcelona, Barcelona, España IQVIA A tiempo completoClinical Research Associate RoleIQVIA is seeking a talented and motivated Clinical Research Associate to join our Sponsor dedicated team. As a junior CRA, you will have the opportunity to gain experience in a wide variety of therapeutic areas and build a strong career within our organization.Key Responsibilities:Conduct site selection, initiation,...
-
Clinical Research Associate
hace 2 semanas
Barcelona, Barcelona, España IQVIA A tiempo completoClinical Research Associate RoleIQVIA is seeking a talented and motivated Clinical Research Associate to join our Sponsor dedicated team. As a junior CRA, you will have the opportunity to gain experience in a wide variety of therapeutic areas and build a strong career within our organization.Key Responsibilities:Conduct site selection, initiation,...
Global Study Associate
hace 3 meses
Job Description:
At AstraZeneca, we are guided in our work by a strong set of values, and we're resetting expectations of what a bio-pharmaceutical company can be.
From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that transform lives.
We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.
If you're swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person.
Accountabilities/Responsibilities:
- Contribute to clinical study startup, execution, closeout and reporting
- Collect, review and track regulatory and other relevant documents. Interface with Investigators, Strategic Partners, Site Management & Monitoring and internal staff during the collection process to support effective delivery of a study and its regulatory documents through finalization of the Clinical Study Report (CSR)
- Initiate and lead the setup of the electronic Trial Master File (eTMF) including tracking of documents. Maintain and close the eTMF ensuring International Conference of Harmonisation Guidelines for Good Clinical Practice (ICH/GCP) compliance
- Initiate and maintain production of study documents, ensuring template and version compliance
- Create and/or import clinicalregulatory documents into the Global Electronic Library (GEL) according to the Global Document List (GDL) and maintain documents according to current process ensuring compliance with the AstraZeneca Authoring Guide for Regulatory Documents to support publishing in GEL
- Plan and proactively collate the administrative appendices for the CSR
- Interface with Data Management Centre and/or Data Management Enablement representatives to facilitate the delivery of study related documents
- Coordinate administrative tasks during the study process, audits and regulatory inspections, according to company policies and SOPs
- Prepare, contribute to and distribute presentation material for meetings, newsletters and websites
Minimum Requirements
Education and Experience
-
Relevant experience from within the pharmaceutical industry or similar organization, preferably of at least 1 years - knowledge of clinical development / drug development process in various phases of development and therapy areas;
- Level of education that supports Skills and Capabilities of the position and ensures successful conduct of accountabilities/responsibilities and appropriate interactions with internal/external customers
- Proven organizational and analytical skills
- Previous administrative training/experience
- Computer proficiency
- Excellent knowledge of spoken and written English
- Project management experience desirable
- Develop working knowledge of the Clinical Study Process and an understanding of the range of working procedures relating to it, together with an understanding of the ICH/GCP guidelines
- Ability to develop advanced computer skills to increase efficiency in daytoday tasks
- Excellent verbal and written communication and presentation skills
- Demonstrate ability to work independently, as well as in a team environment
- Ability to prioritise and manage multiple tasks with conflicting deadlines
- Good interpersonal skills and ability to work in a team environment
