13.06.2025 | Full-time | InderoThe Central Monitoring Manager is responsible for the strategic and operational oversight of centralized monitoring activities across studies, from study start-up through database lock. This includes leading the development and implementation of study-specific centralized monitoring plans
Uita-te mai târziu13.06.2025 | Full-time | InderoThe Senior Project Assistant works with Project Managers, Project Coordinators and Clinical Research Associates (CRA) at many stages during clinical studies. Works independently to coordinate and manage study deliverables and administrative tasks, as required by the project team. More specifically
Uita-te mai târziu12.06.2025 | Full-time | SchaefflerStakeholders Support in the development of training courses in the area of occupational safety Collaboration in interdisciplinary, overarching, international working groups Your profile Degree in mechanical engineering, occupational safety or a comparable course of study Several years of professional
Uita-te mai târziu12.06.2025 | Full-time | InderoAnd oversight of the clinical investigative sites as well as the clinical monitoring deliverables the trials. The APM, EPTR must ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard operating procedures (SOPs), good clinical practices, regulatory
Uita-te mai târziu12.06.2025 | Full-time | Cotnari | LONDON SCHOOL OF EXCELLENCE LTDRemote role based in Romania, offering an exciting opportunity to help students achieve their educational goals in the UK. Tasks - Serve as the first point of contact for Romanian-speaking students interested in studying in the UK. - Provide clear, accurate information about UK university programs
Uita-te mai târziu12.06.2025 | Full-time | PSI CROJob Description As a Clinical Supplies Specialist, you will be contributing to the smooth conduct of global clinical trials, ensuring high-quality clinical supplies flow, and be involved in something new, outstanding and challenging. Hybrid role Bucharest, Romania Responsibilities - Clinical study
Uita-te mai târziu12.06.2025 | Full-time | ElfieTeam, culture, and what it's like to relocate to Vietnam? Click to find out more on our careers page! About The Role The Product Manager for Elfie Research will design and deliver study-specific product experiences that align with clinical protocols while keeping participants engaged. You’ll bridge
Uita-te mai târziu11.06.2025 | Full-time | ParexelAnd according to the assigned role (Global Lead Physician or Regional Lead Physician) Participate actively in study planning with feasibility leaders, solution consultants Participate in team project and investigator meetings Provide training of study teams on TA indication and protocol (Note that this does
Uita-te mai târziu11.06.2025 | Full-time | TFS HealthScienceTo demonstrating credibility and depth of knowledge to potential sponsors. We are looking for someone confident, articulate, and experienced enough to engage with clients at a high level and reinforce the strength of our clinical team. This role is pivotal in shaping study design, leading bid defenses and ensuring
Uita-te mai târziu11.06.2025 | Full-time | StefaniniJob Details Software Tester - determined 2 years Job Description Ensure the correct functioning of clinical trial software with focus on patient safety and integrity of clinical study data Verify that requirements are clear, testable, and consistent with the clinical trial protocol Ensure all
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