A clinical research organization needs applicants for an opening for a Telecommuting Senior Project Data Manager. Individual must be able to fulfill the following responsibilities: Dveeloping effective project plans. Effectively planning and executing multiple Data Management projects.
A healthcare company is seeking a Telecommuting Senior Project Data Manager. Individual must be able to fulfill the following responsibilities: Acting as Project Leader on a stand alone contract. Acting as Functional Lead for Data Management on full service contracts.
A biotechnology company is searching for a person to fill their position for a Lead Data Manager- Home Based Contract Part Time Functional Services United States. Core Responsibilities of this position include:
Candidates will be responsible for the following: Gathering and analyzing data. Utilizing Interest in consumer finance. Position Requirements Include: Must be able to gather and analyze data. An interest in consumer finance is a must. Must love data and critical thinking.
Responding to inquiries quickly and accurately. Creating and maintaining reports that record data and produce relevant documentation from primary and secondary data sources. Maintaining data integrity and ongoing quality control of delivered reports. Position Requirements Include:
A data and analytics provider is seeking a Telecommute Construction Information Research Reporter in Madison. Core Responsibilities Include: Collecting information, documents and other customer requirements within assigned territory.
Design study questionnaires and perform in-depth quality checks and data verification. Support the launch and ongoing maintenance of research studies. Must meet the following requirements for consideration: Must attend quarterly meetings.
Co-monitoring visits or coordinating Data Verification Initiatives. Proactively identifying country related issues and developing the Country Corrective Action and Preventive Action Plans. Must meet the following requirements for consideration: Able to travel to perform co-monitoring visits.
Supporting the collection of data for regulatory filings. Conducting state - specific legal research and monitor changes in requirements to mitigate risks and achieve compliance. Supporting development and response to State and Federal regulatory requirements.
Extensive global clinical trial/study management experience. Working knowledge of Good Clinical Practices, monitoring, clinical and regulatory operations. Country-level cultural awareness and strong interpersonal skills. Ability to interpret study-level data & translate and identify risks.