Clinical Research Associate
17 hours ago
IQVIA is looking for a Clinical Research Associate to provide service to the multisponsor team.
You would be responsible for:
- Performing visits (such as selection, initiation, monitoring and close-out) according to ICH-GCP guidelines.
- Support of the site(s) i.v.m. patient recruitment.
- RCA and CAPA management.
- Reporting of visits and progress of the studies.
- Management and archiving of study documents in eTMF.
- Collaboration with the project/study team.
- Documentation in Monitoring Visit Reports and follow-up letters.
We are looking for:
- MSc and/or BSc education level. Preferable in Health Sciences.
- Proficient level of Romanian and English.Romania based.
- Good knowledge and application of ICH-GCP.
- Minimum of 1 year of experience as a CRA.
- Experience in using CTMS, eTMF and EDC systems.
- Experience in different studies, phases, visits and therapeutic indications.
- Passion for science, helping patients and collaborating with the sites.
- Availability to travel across the country, driving license.
What we offer
- Working with one of the TOP 5 sponsors globally on international projects.
- Focus on quality, not quantity We invest in keeping our teams stable, so workload is consistent.
- The chance to work on cutting edge medicines right at the forefront of drug development.
- Genuine career development opportunities for those who want to grow as part of the organization.
- Flexible conditions and an attractive remuneration package.
- Hybrid model, office based and home based roles available
We invite you to join IQVIA
- FORTUNE Magazine's World's Most Admired Companies list for the third year in a row (January 2020)
- Recognized by the 2016 Scrip Awards as the Best Full-service Provider Contract Research Organization (CRO)
- Awarded the 2016 Eagle Award from the Society for Clinical Research Sites (SCRS) for the fourth consecutive year.
- A site-nominated award recognizing contract research organizations (CRO) and biopharmaceutical sponsors dedicated to building positive relationships with research sites through leadership, professionalism and integrity .
- IQVIA named in The International Association of Outsourcing Professionals (IAOP) 2017 Global Outsourcing 100 List which recognizes the world's best service providers across a range of industries.
We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us . You will have the opportunity to play an important part in helping our clients drive healthcare forward and whatever your career goals, we are here to ensure you get there
Are you interested or do you know the ideal candidate?
- If you know the right candidate or for more information on this role please contact
- Please note is necessary that your application is registered in our Talent Network to process your candidacy
IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more
-
Clinical Trial Web Application Developer
18 hours ago
Bucharest, , Romania Everest Clinical Research Full time 30,000 - 60,000 per yearEverest has been a CRO since January 2004 with a strong foundation as a statistical, programming, and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Headquartered in Toronto, Canada, with subsidiary offices in New Jersey, USA; Shanghai, China; Taipei, Taiwan;...
-
Freelance Clinical Research Associate
17 hours ago
Romania Rho Full time 15,000 - 30,000 per yearJoin us in redefining what it means to work for a CRO. When you work at Rho, it's more than just a job—you become part of the Rho Factor. We're a proud bunch of science nerds who love tackling big challenges together. We're not your typical CRO, and we're not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is...
-
Regional Clinical Product Marketing Specialist
17 hours ago
Greece or Romania Mindray Medical Full time €40,000 - €80,000 per yearRegional Clinical Product Marketing Specialist – (Anaesthesia & Ventilation)Covering Southeast EuropeLocation: Greece or RomaniaDepartment: Medical Devices – Patient Monitoring & Life Support (Anaesthesia, Ventilation, Defibrillation, Infusion & Surgical)Type: Full-Time | Field-Based | Travel RequiredAbout the RoleAre you passionate about advancing...
-
Clinical Systems Specialist-ROMANIA
17 hours ago
Romania Indero Full time 15,000 - 30,000 per yearThe Clinical Systems Specialist is responsible for providing support to internal end users for the Clinical Systems including training, troubleshooting, reporting, and managing user access.More specifically, the Clinical Systems Specialist:Manage and support the Clinical Systems, including system implementation, set-up, maintenance, support, training,...
-
Brand and Market Researcher
17 hours ago
Romania Superbet Full time 20,000 - 40,000 per yearIt's an exciting time to join Superbet, we're entering new markets, developing new technologies, and moving step by step towards our goal of exciting the world. As our business grows, the number of exciting people initiatives grows with it, and we're looking for a new colleague to partner with our team to bring these to life.We're looking for a Brand and...
-
Associate Director, Pharmacovigilance Safety
17 hours ago
Romania Who we are Teva Full time 40,000 - 80,000 per yearWho we are Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day....
-
Drug Device Safety Officer I
17 hours ago
Romania Premier Research Full time 25,000 - 35,000 per yearPremier Research is looking for a Drug Device Safety Officer I to join our Pharmacovigilance and Records Management team.You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we...
-
Site Selection Specialist
17 hours ago
Romania Indero Full time 15,000 - 30,000 per yearThe Site Selection Specialist is a key collaborator to project teams as the main point of contact for site selection activities (including site identification and feasibility).This role is perfect for you if:You have experience working with clinical research sites;You want to work in a collaborative environment;You want to have an impact in a fast-growing...
-
Senior Regulatory Affairs Associate
18 hours ago
Romania-Bucharest-Metropolis Center Parexel Full time €30,000 - €60,000 per yearWhen our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...
-
eCOA & RTSM Application Specialist (Romania)
17 hours ago
Romania Indero Full time 30,000 - 60,000 per yearThe eCOA and RTSM Application Specialist is responsible for supporting the design, deployment, configuration, and oversight of electronic Clinical Outcome Assessment (eCOA) solutions—including ePRO, eConsent, and other patient-centric electronic data capture tools— and of Randomization and Trial Supply Management (RTSM) across global clinical...