JOB PURPOSE / SUMMARY This person will serve as the primary CTI Clinical Data Management (CDM) contact with sponsors and represent the DM group on CTI project teams. Responsible for study-specific CDM document development and maintenance, project status to
What Youll Do: Conduct pre-entry review of clinical data Review and issue queries for case report form (CRF) data based on automated edit checks, manual review, and sponsor requirements Assist with set-up of data management study files and the collection, transfer,
Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and
Learn about knok At knok, we dare to lead and humanise the digital transformation of healthcare. We envision a world where everyone has timely access to quality healthcare through digital technology, creating a more equal society.
About Unilabs Headquartered in Geneva and part of the A.P. Moller Group, Unilabs is one of Europe’s leading medical diagnostics companies, offering a complete range of laboratory, pathology, genetics, and imaging services to patients across 14
What Youll Do: Perform medical monitoring activities under the oversight of a medical director. Medical monitoring activities include but not limited to review of the protocol and investigator’s brochure, review of medical budgets, preparing the medical
Company Description PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and
IQVIA is the world leader in the provision of health and pharmaceutical data to the health care sector. Our Real-World Solutions (RWS) department is globally renowned for providing business focused research, conducted to the highest standards. IQVIA
Job Summary: Supports the execution, operationalization, sustainability, and continuous improvement of CTI’s Risk-Based Quality Management framework across the clinical trial portfolio. This role supports the Director, RBQM by coordinating Integrated Quality and Risk Management Plan activities, facilitating cross-functional risk
At Solventum, we improve lives by helping healthcare professionals do their best work. Join a team using innovation and insight to make a real impact on the future of healthcare. All roles listed are with Solventum,
Learn about knok At knok, we dare to lead and humanise the digital transformation of healthcare. We envision a world where everyone has timely access to quality healthcare through digital technology, creating a more equal society.
Clinical Research Associate Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits after completing training period Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance
Company Description Hello! Were looking for an awesome Talent Acquisition & Operations Specialist | Deep-Tech / AI @ Personalized Medicine to join our team on our journey to revolutionize personalized medicine Job Description Were looking for
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our
At Sword, we’re building AI to heal billions and unlock humanity’s full potential. In doing so, we’re pioneering AI Care, a fundamentally new approach to healthcare built for medical reasoning, safety, and real-time treatment, not generic
As a Customer Experience Analyst, you will be responsible for supporting IQVIA clients in maximizing the value of our data, solutions and services. Acting as a trusted point of contact, you will help ensure service excellence, client
Psychologist or Psicólogo - Lisbon - Affiliate Application Deadline: 31 October 2026 Department: Clinical Employment Type: Freelance Location: Lisbon Description Job Title: Psychologist or Psicólogo Location: Lisbon Portugal Contract Type: Affiliate Contract Work Type: Onsite Work Hours:
Company Description Medicine moves forward here. So will you. At PrimeVigilance, patient safety is not one part of the job. It is why we exist. We are a global pharmacovigilance specialist. Our teams help clients navigate
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our
Description Projects Managers with experience in Dermatology and/or Rheumatology are crucial to the success of Clinical Trials managed by Indero. They are the main point of contact internally as well as externally, ensuring all activities and deliverables