07.06.2024 | Full-time | ParexelResponsibilitiesPartners with study teams, with responsibility management of required regulatory activities, standards and deliverables associated with CTA submission development and completion of relative associated documentation as and attends relevant meetings to advocate
Uita-te mai târziu07.06.2024 | Full-time | BoschAnd tracking of the solutions;You will be in charge to train the key-users (training on operational processing and country-specific developments).QualificationsEducation Degree in business administration or comparable field of study;Personality convincing, open-minded character who communicates
Uita-te mai târziu07.06.2024 | Full-time | IQVIAActivities in accordance with Study Protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (ICH GCP) and applicable regulatory requirements. Gain an understanding of all aspects of Real-World Late Phase Research, Site Management and Site onsibilities Develop an understanding
Uita-te mai târziu07.06.2024 | Full-time | AbbVieClinical trial data and participates in applicable safety surveillance activities for assigned studies including review and contribution to ad-hoc Safety Reports as needed. - Provide review and analysis of safety-related data from clinical trials for content, quality, potential study level trend
Uita-te mai târziu07.06.2024 | Full-time | PharmiwebOf the trial (investigator meetings, site visits, quality communication, etc.). Drive study compliance by executing activities within site initiation and start-up, site monitoring, site management and site/study close-out according to internal SOPs and policies. Ensures site staff is trained
Uita-te mai târziu07.06.2024 | Full-time | Signant HealthThe Best Team of your life?We're on the hunt for a new Localisation Specialist for one of our Global Support Services teams in Iasi working on the Operations area of the business. The position gives you a great view on how a clinical study is being set up.The team is accountable for successful delivery
Uita-te mai târziu07.06.2024 | Full-time | PharmiwebYou’ll do Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports. Build relationships. Oversee integrity of the study and utilize problem-solving skills
Uita-te mai târziu07.06.2024 | Full-time | PSI CROAnd investigators. Your focus will be on subjects’ rights, safety and well-being and quality of data compliance. Your responsibilities will include Conducting and reporting all types of onsite monitoring visits Driving the study startup phase (if applicable) Performing CRF reviews, source document verification
Uita-te mai târziu07.06.2024 | Full-time | Linde Gaz Romania SRLAnd continuously identifying sales projects and opportunities Active assistance for the reinforcement of existing partners´ loyalty The management of the bids and direct procurement procedures organized by the contracting institutions You will also develop and streamline the activity of Sleep Study Laboratories
Uita-te mai târziu07.06.2024 | Full-time | UiPathOn Inside UiPath What you'll bring to the team1-2 years experience in a deal/licensing support or sales support role OR a bachelor’s degree in a like field of studyFluent written and spoken English; German is preferableExperience with general productivity tools such MS office, G-sheets, rience
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