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- ...and the wider organization, such as Quality Assurance. • Coordinate and support Hub & Country related audits & inspections (e.g. Clinical Development Audit, Investigator Site Inspection) as per selection and scope, from preparation to CAPA & effectiveness checks...
- ...Manager Massive Bio is a rapidly growing health-tech startup founded in New York to provide every cancer patient with access to clinical trials regardless of their location or financial stability. Our proprietary patient recruitment and enrollment enablement...
- Massive Bio is a rapidly growing health-tech startup founded in 2015 to provide every cancer patient with access to clinical trials regardless of their location or financial stability. Our proprietary patient recruitment and enrollment enablement solution for oncology...
- Massive Bio is a rapidly growing health-tech startup founded in 2015 to provide every cancer patient with access to clinical trials regardless of location or financial situation. Our proprietary patient recruitment and enrollment enablement solution for oncology clinical...
- ...Massive Bio is a rapidly growing health-tech startup founded in 2015 to provide every cancer patient with access to clinical trials regardless of their location or financial stability. Our proprietary patient recruitment and enrollment enablement solution for oncology...
- ...Analytics Massive Bio is a rapidly growing health-tech startup founded in 2015 to provide every cancer patient with access to clinical trials regardless of their location or financial situation. Our proprietary patient recruitment and enrollment enablement solution...
- ...verification. Selected candidates may be required to provide additional information within the scope of background check. CLINICAL DIRECTOR Position Title: Clinical Director Project Location: İstanbul, Türkiye Reports to: General Manager Contract...
- ...Work Schedule Standard (Mon-Fri) Environmental Conditions Office Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close...Uzaktan çalışma
- (CRA II or above, Several sites across Türkiye) Responsibilities: Perform all types of monitoring visits (site selection, initiation, routine, and close-out) in line with ICH-GCP, protocol requirements, and SOPs Independently manage assigned study sites to ...
- ...we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions. Field Clinical Specialist Graduate Working in our Rhythm Management division, you will be working daily in hospital Cath Labs or operating...
- ...To enable AbbVie’ s emergence as a world class R&D organization, the position anticipates and proactively solves study-related clinical site issues as they occur and initiates, recommends and communicates corrective action ensuring successful protocol level execution...
- ...responsibilities are: Actively engages with sites and CROs to maintain and influence a positive operational environment for clinical trials in the Turkey Managing day-to-day clinical activities, including protocol amendments, data review, and communication...
- ...Our client, a global leader in medical device manufacturing, is seeking a Clinical Application Specialist in Istanbul, Türkiye. As a Clinical Application Specialist, you will oversee all product-related marketing and application activities for our client's surgical...
- ...As a Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: P l a n n i n g , m a n a gement, and o v e r s i g...
- Clinical Scientist (EMEA, NA, LATAM) - Sponsor - dedicated Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes...
- ...Senior Clinical Research Associate IQVIA is the Human Data Science Company oriented to drive human health outcomes forward. When you join IQVIA Turkey as a sponsor-dedicated CRA, you'll enjoy the stability and resources of a leading, global contract research organization...
- ...Job Overview Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project...
- ...Clinical Research Associate IQVIA Turkey is looking for talented and motivated team member to join our Sponsor dedicated team as junior CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience...
- ...provides you with the opportunity to gain relevant, project-based work experience at one of the most successful and cutting-edge global clinical research units in the market while building relationships within the company that will impact their futures. We currently are...
- ...role offers a unique opportunity to contribute to cutting-edge health-tech solutions aimed at transforming cancer patient access to clinical trials. You will work closely with cross-functional teams to develop advanced machine learning models, design innovative...
- ...perspective through scientific exchanges with payors, hospital pharmacists and others, Maximize site performance and support clinical trials, non-interventional and other RWE studies through the collection and communication of medical and scientific knowledge,...
- ...ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products that meet customer needs. Provide leadership and...
- ...should be collaborative. Perform other duties as directed by Line Manager. Qualifications ~ Bachelor's Degree In health, clinical, biological or mathematical sciences, or related field with proven experience in Data Management Req ~3 -4 years direct Data...
- ...As a CTA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: Working fully outsourced at one of our global pharmaceutical clients, the Clinical Trial Assistant plays...
- ...performance metrics, ensuring compliance with healthcare regulations and standards. - Collaborate with internal teams, including clinical and IT departments, to ensure timely and effective service delivery. - Identify opportunities for upselling and cross-selling...
- ...is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Every day we perform better because...
- ...is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings...
- ...to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating...
- ...CRA role, to really be an expert on your protocols and to own your sites. Summary of Responsibilities Manage all phases of clinical site activity: pre-study, initiation, monitoring, and close-out visits Ensure protocol compliance, data accuracy, patient safety...
- ...expert on your protocols and to own your sites. Summary of Responsibilities: Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard Operating Procedures (SOPs), ICH guidelines and GCP; including Pre-study, Site Initiation,...