Clinical Trial Data Management Jobs

Thor Companies - Boston, MA, United States

of clinical trial protocols • Oversee, develop and maintain study-specific documentation, including Data Management Plans, eCRF specifications, CRF Completion Guidelines, Data Validation Guidelines, Data

from: linkedin.com - 2 days ago

Investigators Research Group, LLC - Brownsburg, IN, United States

coordination or a related role Knowledge of Good Clinical Practice (GCP) guidelines and the regulatory environment for clinical trials Familiarity with research methodologies and data collection techniques

from: linkedin.com - Yesterday

Meet - , TX, United States

to protocol, budget, and timelines. Coordinate cross-functional teams, including Clinical Operations, Data Management, Regulatory Affairs, and Medical Affairs, to drive study milestones and deliverables

from: linkedin.com - 2 days ago

Medix™ - Peoria, IL, United States

and metric data as it relates to clinical trial activities. The CRB Analyst also assists with clinical trial billing special projects, ensures timely invoicing, monetary disbursing and tracking, and monitoring

from: linkedin.com - 2 days ago

Medix™ - Warrenville, IL, United States

control procedures to ensure accuracy and completeness of data. Maintain organized and secure study-related documentation. Clinical Trial Coordination: Assist in coordinating study visits, scheduling

from: linkedin.com - 2 days ago

Bicara Therapeutics - Boston, MA, United States

. Qualifications Bachelor's Degree is required, preferably in Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy). Minimum of 2-5 years clinical trial management experience

from: linkedin.com - 2 days ago

Medasource - , OR, United States

. Perform medical review and safety analysis of clinical trial subjects; including periodic completion of the Safety Management Plan for individual trials. Assist in the determination whether new safety

from: linkedin.com - 6 days ago

Life Science People - Durham, NC, United States

III. Collaborate with cross-functional teams, including Clinical Development, Regulatory Affairs, and Data Management, to ensure seamless trial progression. Regulatory Compliance: Ensure compliance

from: linkedin.com - 5 days ago

i-Pharm Consulting - Trenton, NJ, United States

of experience in clinical operations, with at least 7 years of specialized experience in global study management. Responsibilities: Lead and oversee the operational execution of global clinical trials, ensuring

from: linkedin.com - 5 days ago

Beacon Hill - , MA, United States

, and cleaning of clinical trial data, in collaboration with relevant members of the cross-functional clinical trial team, including Clinical Operations and Data Management. Authoring clinical sections

from: linkedin.com - 6 days ago