Clinical Data Quality Associate

**Job Overview** The Sr. Clinical Data Coordinator performs activities related to the conduct of Phase I - III clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines. This role ensures that quality work products are produced, and timelines and deliverables are met. **This position can typically be a...

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives. ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing...

Mexico, Remote **Job ID** R0000028057 **Category** Data Management **ABOUT THIS ROLE**: We are looking for Clinical Data Analyst II (CDAII) to join our team in Mexico. CDA will perform clinical data validation activities independently, supports data validation and documentation tasks. Additionally, it will adhere to quality standards, SOPs, ICH-GCP, and...

**Job Overview** The Clinical Data Manager (CDM) is responsible for managing data activities for Phase I-III clinical trials, ensuring compliance with ICH/Good Clinical Practices (GCP) and other relevant guidelines. The CDM ensures trials are completed on time, within budget, and with the highest quality. **Key Responsibilities**: - Serve as the primary...

Mexico, Remote **Job ID** R0000028052 **Category** Data Management **ABOUT THIS ROLE**: Key Accountabilities: - Data Validation: Lead data cleaning, review, and reconciliation activities. - Documentation: Prepare and maintain DM documents as per SOPs and guidelines. - Study Start-Up: Conduct UAT on clinical database setups and review protocols. Quality...

**Work Schedule** Other **Environmental Conditions** Office At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve...

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...

As a Medical Data Reviewer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will have the opportunity to gain experience working with a large biotech company, a pioneer and industry leader in the area of Antibody research, that utilizes their innovative technology platform...

**Assoc. Clinical Operations Lead** **Essential Functions**: - Oversee the delivery of Site Management project tasks, providing advice and guidance to achieve high performance and quality project deliverables. - Ensure overall project efficiency and adherence to project timelines and financial goals; report metrics and out of scope activities. - Develop,...

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center of all that we do, we help to accelerate the development...

We are currently seeking a Clinical Study Manager II to join our diverse and dynamic team. As a Clinical Study Manager II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies. **What you will be doing**: - Lead the...

**Job Overview** Perform daily administrative activities in collaboration with Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) teams to ensure the accurate delivery of the Trial Master File (TMF). **Essential Functions** - Assist CRAs and RSU teams with updating and maintaining clinical documents and systems (e.g., TMF) to track site...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Clinical Team Manager** PPD’s (a part of Thermo Fisher Scientific) mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it’s you! We know that meaningful results not only require the right approach, but also the right...

**Based in Mexico for Sponsor Dedicated** **Job Overview** Manage a team of clinical staff working in support of clinical studies for Sponsor Dedicated model, to ensure projects are appropriately resourced and employees are trained and meeting project objectives. **Essential Functions** - Manage staff in accordance with organization’s policies and...

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center of all that we do, we help to accelerate the development...

projects are appropriately resourced and employees are trained and meeting project objectives. Essential Functions - Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work, assessing performance and guiding professional development, rewarding and disciplining...

**Job Overview** In-depth knowledge of applicable global, regional and local clinical research regulatory requirement; i.e. Good Clinical Practice (GCP) and International. Provide departmental support to Clinical Event Validation and Adjudication (CEVA) Management and project support to CEVA Project Managers/Leads. Support provided is typically broad in...