Senior Study Start Up Associate

Description ̈ Collect, track and perform a quality review of all essential & investigator documents required for effective and compliant study site activation and maintenance ̈ Ensure that all assigned maintenance and Start-up activities are on track and in accordance with client expectations, ICH/GCP, SOPs, budget, quality and applicable laws and...

̈ Collect, track and perform a quality review of all essential & investigator documents required for effective and compliant study site activation and maintenance ̈ Ensure that all assigned maintenance and Start-up activities are on track and in accordance with client expectations, ICH/GCP, SOPs, budget, quality and applicable laws and guidelines ̈ Serve...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Help create a healthier world: START RIGHT HERE AT IQVIA.Proficiency in English, both verbally and written are necessary.Please submit resume in English.Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs),...

Job Description To enable AbbVie' s emergence as a world class R&D organization, the position plays a key role in ensuring successful protocol level execution of CSM deliverables involving start-up, execution, and close-out of studies.Responsibilities:For assigned sites/study(s), ensure successful protocol level execution of CSM deliverables involving...

Company DescriptionTo enable AbbVie' s emergence as a world class R&D organization, the position plays a key role in ensuring successful protocol level execution of CSM deliverables involving start-up, execution, and close-out of studies.Responsibilities: For assigned sites/study(s), ensure successful protocol level execution of CSM deliverables involving...

Study Lead - South America Grow your career and project management expertise as part of the Rio Tinto Studies Team Join a global leadership group that is safety focused and values inclusive Based in Santiago, ChileAbout the roleFinding better ways to provide the materials the world needsWe are looking for a Study Lead to support our growing portfolio of...

The Clinical Research Associate II (CRA II) is responsible and accountable for site monitoring and site management. Has responsibility for clinical studies according to Company, and/or Sponsor Standard Operating Procedures, and local regulatory guidelines. Assures the implementation of project plans, as assigned. Act in the project role of a Local Project...

Job DescriptionWith support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites.• Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.• Performs clinical study site...

Job DescriptionWith support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites.• Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.• Performs clinical study site...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.With our patients at the centre of all that we do, we help to accelerate the development...

Are you passionate about education and travel?We are Southbridge Access, an Educational Tourism Company that creates turnkey solutions for faculty-led programs. We are currently looking for our next Costing Associate for our Operations Department.The objective of the position is:Source and update every needed quote for SBA programs in direct contact with...

At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives.Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration,...

Job Description:This role is responsible for comprehensive trial and site administration. Under the oversight of the Senior COM or COMs, the person prepares, collates, distributes and archives clinical documents.The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.The...

Job Description:The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our policies and procedures, quality standards and adverse event reporting requirements internally and externally....

Company DescriptionWe are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

Job ID- #BH-671 Category Consulting and Strategy,Engineering & Maintenance,Mining Location Chile, Chile Job Type Full Time Posted Date 21 July 202 Closing Date 18 August 2023The CompanyGlobe 24-7 in partnership with a key client in Santiago are working together to source a highly capable and motivated professional to join our LATAM Resources Engineering...

With support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site management/monitoring activities...

Join Our Team as a Senior Developer in the European Energy SectorProductized, a software development company based in the Netherlands, is seeking a skilled Senior Developer to contribute to our projects in the European energy sector.About the ProjectIn this project, we will partner with a stock-listed company to develop cutting-edge tools aimed at...

Job DescriptionDescription –>Under the supervision of a head of office, the Executive Associate is accountable for procedural communications, operations and administrative support services, as well as specialized administrative functions, to enhance the smooth running of the supervisor's day-to day activities, as well as his/her section. Executive...