Sr. Manager, Clinical Data Management

PPD’s 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 people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams. Our...

**Job Description**: The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our policies and procedures, quality standards and adverse event reporting requirements internally and...

Maintaining the highest level of quality in clinical trials is crucial for patient safety and data integrity. As a Country Clinical Quality Manager, you will be instrumental in achieving this goal.You will work closely with the Regional Director, Clinical Quality Management, to oversee all Clinical Quality Management activities in the respective...

Clinical trials require meticulous attention to detail to ensure patient safety and data integrity. As a Country Clinical Quality Manager, you will be responsible for overseeing Clinical Quality Management activities in the respective country/cluster.You will work under the guidance of the Regional Director, Clinical Quality Management, to develop and...

It is critical that, for all company-sponsored clinical trials, patient safety, high quality data and compliance with company requirements and regulations are delivered and sustained. The CCQM position has a significant impact in achieving those objectives. Under the guidance of the Regional Director, Clinical Quality Management (RCQM), the CCQM oversees...

As a Clinical Site Monitoring Services Manager at Alimentiv Inc, you will be responsible for overseeing the full clinical site monitoring services for one or more projects. This may include multiple services, complex in nature, and/or running on a multinational scale.Key Responsibilities:Manage and deliver project monitoring services, ensuring compliance...

CRA with a minimum of 4 years acting as primary site contact and site manager (monitoring) in a bio/pharma/CRO. Fluent in Local Language and English (verbal and written) and excellent communication skills. **Responsibilities include, but are not limited to**: - Develops strong site relationships and ensures continuity of site relationships through all...

At ICON, we are seeking a highly experienced Senior Clinical Research Associate to join our dynamic team. The ideal candidate will have a strong background in clinical trial management and a proven track record of ensuring study integrity and compliance.Job Description:The Senior CRA will be responsible for overseeing and managing clinical trial activities...

At Johnson & Johnson, the largest healthcare company in the world, we come together with one purpose: to profoundly change the trajectory of health for humanity. Diversity & Inclusion are essential to continue building our history of groundbreaking and innovation, which has been impacting the health of more than 1 billion patients and consumers every day...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

As a Country Clinical Quality Manager at Merck Gruppe - MSD Sharp & Dohme, you will play a pivotal role in ensuring the highest standards of quality in clinical trials.The position has a significant impact on achieving patient safety, high-quality data, and compliance with company requirements and regulations.You will oversee all Clinical Quality Management...

At ICON, we are looking for a skilled Clinical Trial Program Manager to join our team. As a key member of our global clinical operations team, you will be responsible for planning, management, and oversight of clinical study execution in accordance with the global program strategy.Your responsibilities will include:Leadership of the cross-functional Local...

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where our company has codified its 125-year legacy. Our company success is backed by ethical...

**Senior Clinical Research Associate** (Level dependent on experience)** **Please submit your CV in English for Quickest Review Process!** Maintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so, we have weekly all-staff meetings in which each department can...

**Senior Clinical Research Associate** **(Level dependent on experience)** Maintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so, we have weekly all-staff meetings in which each department can provide an update on a study or milestone that they have achieved....

**JOB DESCRIPTION**: This business-critical position provides extensive statistical and data programming support across multiple projects within the Evidence Synthesis, Modeling & Communication (EMC) - Clinical Outcome Assessment (COA) team. The EMC COA team largely designs and conducts statistical analyses of COA data, including patient-reported outcome...

DATA MANAGEMENT II PROYECTOS CDO Country: Chile **WHAT YOU WILL BE DOING** Desde la gerencia del Chief Data Officer (CDO), en el equipo de proyectos Big data, estamos buscando un Data Manager que tenga como rol principal liderar todas las iniciativas relacionadas a datos con el objetivo de afianzar la estrategia corporativa de los ambientes de Big Data...

Job Description It is critical that, for all company-sponsored clinical trials, patient safety, high quality data and compliance with company requirements and regulations are delivered and sustained. The CCQM position has a significant impact in achieving those objectives. Under the guidance of the Regional Director, Clinical Quality Management (RCQM),...

Sr. Data Architect , Professional Services Job ID: 2901081 | Amazon Web Services Argentina S.R.L. - F61 The AWS Professional Services organization is a global team of experts that help customers realize their desired business outcomes when using the AWS Cloud. We work together with customer teams and the AWS Partner Network (APN) to execute enterprise...

We are seeking a highly motivated and experienced Clinical Operations Manager to join our global clinical team. As a key member of our team, you will be responsible for the overall management of clinical research studies, including staff supervision, resource allocation, and project coordination.About the RoleThis position requires strong leadership and...