The Clinical Data Manager (CDM) is responsible for the oversight, integrity, and quality of clinical trial data from collection through database lock. Oversee data cleaning activities, including the g...

The Design Program Manager role is critical to ensuring Audible design and research teams deliver exceptional user experiences through operational excellence. As a UX Design Program Manager, you will.

This role will represent the voice of the customer, partnering with Engineering, Data Science, Brand, Creative, and Marketing to define a customer-obsessed product roadmap, empowering the organization...

Minimum of 5 years of experience as a Clinical Data Manager in the biopharmaceutical industry. Ensure data quality and accuracy through data review, query resolution, and data cleaning. Develop and im...

The Clinical Data Manager (CDM) is responsible for the oversight, integrity, and quality of clinical trial data from collection through database lock. Oversee data cleaning activities, including the g...

The Design Program Manager role is critical to ensuring Audible design and research teams deliver exceptional user experiences through operational excellence. As a UX Design Program Manager, you will.

Minimum of 5 years of experience as a Clinical Data Manager in the biopharmaceutical industry. Ensure data quality and accuracy through data review, query resolution, and data cleaning. Develop and im...

Deliver clinical healthcare services, including immunizations, diagnostic testing, and medication therapy management.

Deliver clinical healthcare services, including immunizations, diagnostic testing, and medication therapy management.

Minimum of 5 years of experience as a Clinical Data Manager in the biopharmaceutical industry. Ensure data quality and accuracy through data review, query resolution, and data cleaning. Sign in to set...

Minimum of 5 years of experience as a Clinical Data Manager in the biopharmaceutical industry. Ensure data quality and accuracy through data review, query resolution, and data cleaning. Sign in to set...

He/she will be responsible for data management aspects of clinical trials and research, from review of study design and data collection tools through study closeout, including eCRF design and build, d...

He/she will be responsible for data management aspects of clinical trials and research, from review of study design and data collection tools through study closeout, including eCRF design and build, d...

Clinical Data Management and clinical development technology solutions. Understanding of the clinical trial processes, including common data standards (CDISC) and Study Data Tabulation Model (SDTM). R...

Clinical Data Management and clinical development technology solutions. Understanding of the clinical trial processes, including common data standards (CDISC) and Study Data Tabulation Model (SDTM). P...

Oversee the development of CRFs and CCGs with other functional area representatives, ensuring all data management databases are developed and validated. Manage all data management activities according...

Oversee the development of CRFs and CCGs with other functional area representatives, ensuring all data management databases are developed and validated. Manage all data management activities according...

The Lead Clinical Data Manager will independently perform all data management functions to ensure timely and quality database lock for studies conducted in-house and offshore CRO. The Lead Clinical Da...

The Lead Clinical Data Manager will independently perform all data management functions to ensure timely and quality database lock for studies conducted in-house and offshore CRO. The Lead Clinical Da...

Responsible for reviewing the data management documentation, data management plan (DMP), CRF, study database specifications, data validation plan, edit check specifications, data transfer specificatio...

Provide ongoing operational support for Medidata RAVE activities during clinical trial conduct including development of clinical databases and associated external data transfer documents including imp...

Provide ongoing operational support for Medidata RAVE activities during clinical trial conduct including development of clinical databases and associated external data transfer documents including imp...

Follow the processes set forth by the department SOPs and the study Data Management Plan to ensure the highest data quality within the organizations managed databases and for outsourced EDC databases....

Follow the processes set forth by the department SOPs and the study Data Management Plan to ensure the highest data quality within the organizations managed databases and for outsourced EDC databases....

Keeps abreast of industry trends in data mapping, data management, standards compliance methodologies, metadata management and data warehousing. Accountable for ensuring submission data sets conform t...

Keeps abreast of industry trends in data mapping, data management, standards compliance methodologies, metadata management and data warehousing. Accountable for ensuring submission data sets conform t...

Clinical Data Management key focus is to ensure data quality, integrity & completeness of all data types (eCRF and non eCRF) collected in BMS clinical trials from study start to database Lock. This ro...

Clinical Data Management key focus is to ensure data quality, integrity & completeness of all data types (eCRF and non eCRF) collected in BMS clinical trials from study start to database Lock. This ro...

Provide ongoing operational support for Medidata RAVE activities during clinical trial conduct including development of clinical databases and associated external data transfer documents including imp...

Provide ongoing operational support for Medidata RAVE activities during clinical trial conduct including development of clinical databases and associated external data transfer documents including imp...

Under limited supervision, works collaboratively with vendor Project Managers and Clinical Data Managers to assure that Data Management functions are performed in compliance with regulations and accor...

Under limited supervision, works collaboratively with vendor Project Managers and Clinical Data Managers to assure that Data Management functions are performed in compliance with regulations and accor...

Responsible for the initiation and approval of the building, testing and validation of clinical databases, subsequent changes in clinical databases and data validation activities. Leads and performs c...

Responsible for the initiation and approval of the building, testing and validation of clinical databases, subsequent changes in clinical databases and data validation activities. Leads and performs c...

Hands-on experience with tools such as Databricks, Dataiku, ETL technology, programming language (SQL, Python), and AWS cloud platform (S3, Data Lake), Data Lake, Data Warehousing, and analytics infor...

Hands-on experience with tools such as Databricks, Dataiku, ETL technology, programming language (SQL, Python), and AWS cloud platform (S3, Data Lake), Data Lake, Data Warehousing, and analytics infor...

Review CRO Data Management Plans, Data Review Plans and other applicable data management documents for completeness and accuracy. Oversee CRO data management counterparts for assigned clinical trials ...

Review CRO Data Management Plans, Data Review Plans and other applicable data management documents for completeness and accuracy. Oversee CRO data management counterparts for assigned clinical trials ...

Invicro is involved in the development and manufacture of radioisotopes for injection into patients/volunteers, as part of clinical programmes. Taking the lead in assembling vials used for clinical pr...

Providing aid/cover for the team as required and to carry out other reasonable duties as requested by the line manager. Ability to organise own assigned activities as well as reporting issues or delay...