Study Start Up Associate I
Frankfurt am Main
Vollzeit
ICON
… & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to … and you’ll be helping shape an industry. The Role: As a member of the Study Start Up Team, you will play an integral role in making sure that … Trial operations and meeting regulatory guidelines Proficient project management skills. Benefits of Working in ICON: Our success depends on the quality of …Clinical Study ManagementData Manager (Clinical Trials)
München
Vollzeit
Medpace, Inc.
… we are currently seeking a full-time, office-based in Munich or home-based Clinical Data Manager to join our Data Management team. This position will work in … and edit checks for the electronic data capture system used for each study; Coordinate overall Data Management by serving as primary contact for the … in Munich or home-based Clinical Data Manager to join our Data Management team. This position will work in a team to accomplish tasks and projects …Study ManagementProject Management Associate (PMA)
Mannheim
Vollzeit
SCOPE International
The organization of international clinical trials requires the development of complex cross-cultural teams across … of project specific procedures Assistance with set-up and maintenance of study specific documentation (trial master file) and tracking tools Quality … setting, coupled with excellent career development prospects and a management culture that is based on an open dialogue. SCOPE International is an …Clinical Study Management
Research Assistant II, Pediatrics Research
Sachsen-Anhalt
Vollzeit
Boston Medical Center
… Makes independent judgements of suitability of potential participants for clinical trials. Conducts the enrollment of study participants, including … assistants. JOB RESPONSIBILITIES: Recruits subjects to participate in the study by using approved methodologies, such as, reaching to healthcare providers … PI and with the oversight of a child psychologist. Data Collection/Data Management Prepares and maintains Institutional Review Board (IRB) approvals and …Clinical Study StellenangeboteClinical Trial Coordinator
München
Vollzeit
Thermo Fisher Scientific
Our team of colleagues in clinical research services are at the forefront of getting cures to market. We … sites to resolve outstanding regulatory issues identified Disseminates study related information, including project tracking updates to Clients, … time Exceptional communication, collaboration, organisational and time management skills. Fluency in English and German, at least to C1 level At PPD we hire …Clinical Management StellenangeboteMedical Writer (MW)
Mannheim
Vollzeit
SCOPE International
The organization of international clinical trials requires the development of complex cross-cultural teams across … Mannheim, Germany is required. Tasks & Responsibilities Develop clinical study documentation, including clinical study reports, subject narratives, … setting, coupled with excellent career development prospects and a management culture that is based on an open dialogue. SCOPE International is an …Clinical Study ManagementClinical Research Manager
Deutschland
Vollzeit
Advanz Pharma
Date: 7 Oct 2023 Location: DE Company: AdvanzPharma Job Title: Clinical Research Manager Location: Germany, UK, Spain About ADVANZ PHARMA ADVANZ … the ability to link with and influence others. What You’ll Do: Clinical study management scope includes mainly biosimilar studies (Phase I PK, Phase III … visible and influential role will involve exposure to Senior and Executive Management and requires an individual with a collaborative approach and the ability …Study ManagementPostdoctoral Researcher (f/m/x)
Bonn
Vollzeit
Deutsches Zentrum für Neurodegenerative Erkrankungen
… strategy comprising five interconnected areas: fundamental research, clinical research, health care research, population health science, and systems … molecular mechanisms underlying aging and neurodegenerative diseases. They study metabolic adaptations that can promote the longevity of animals carrying … to a targeted career development A company pension plan as well as health management A full funded research project, initially limited to two years with the …Study Management StellenangeboteClinical Trial Site Relationship Coordinator
München
Vollzeit
Medpace, Inc.
… Coordinator, or Study Nurse preferred; Knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines … Support management in expediting feasibility, site selection and study start-up; Communication with PI and investigative sites; and May be … Develop effective plans for site contact and follow-up; Support management in expediting feasibility, site selection and study start-up; …Clinical Study Management StellenangeboteSr/CRA Germany
Berlin
Vollzeit
Thermo Fisher Scientific
… research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel … research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and … and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and …Management StellenangeboteClinical Research Associate- Must Be Located in Germany
Homeoffice
Vollzeit
RQM+
… upon 40 years of regulatory expertise, we also provide comprehensive clinical trial, lab and reimbursement services – reducing risk and supporting … Lead CRA to ensure all monitoring activities are conducted according to study requirements. Responsibilities: Participates in the investigator … process and/or study timelines, including updating the study level study management system. Ensures all study deliverables are completed per RQM+ and study …Study Management StellenangeboteClinical Research Associate II
Homeoffice
Vollzeit
ICON
As a Clinical Reserach Associate you will be joining the world’s largest & most … organisation, powered by healthcare intelligence. Key Responsibilities Study Planning Contribute to the identification of new sites for clinical … generate initiation visit report Study Execution Implement complete site management including monitoring visits, regulatory assessment, drug supply …Clinical Study StellenangeboteMathematician - Statistical Programming, Clinical Trials, QC (m/f/d)
Mainz
Vollzeit
BioNTech SE
… Programming Your main responsibilities are: Work collaboratively with Clinical Development team or CRO to meet project deliverables and timelines for … programming deliverables (e.g., analysis datasets, tables, listings) for study reports and integrated summaries Anticipate resource needs and works with … reports and integrated summaries Anticipate resource needs and works with management to ensure adequate long-term resource allocation within a therapeutical …Clinical ManagementLife Scientist - Companion Diagnostics, Performance Studies (m/f/d)
Tübingen
Vollzeit
Immatics Biotechnologies GmbH
… This role will involve, but is not limited to the following tasks: Clinical performance studies under IVDR: Establish and/ or review documentation … functions: Author and/ or review parts of device clinical performance study submission documents (e.g., clinical performance study plan, device … regulatory, commercial, business development, legal, and alliance management functions Your profile Advanced degree in Life Sciences, Biochemistry, …Study Stellenangebote