Clinical Data Manager: Average Salary in Massachusetts in 2024

Senior Manager, Clinical Data Management in Lexington, MA with the following requirements: Master’s degree in Pharmaceutical Sciences, Pharmacology or Toxicology or related field or foreign academic equivalent plus 6 years of related experience. Prior experience must include: Develop and maintain st...

This is an amazing opportunity for a data manager with strong leadership skills to lead projects and supervise a team of Clinical Data Managers. Lead and supervise Clinical Data Managers (CDMs). My client is seeking a professional with excellent communication abilities and a proven track record in c...

Senior Manager/Associate Director - Clinical Data Management. Drive data management strategy within the clinical team. Experience in clinical data management and vendor management. Demonstrated experience in clinical data management. ...

We are looking for a Senior Clinical Data Manager to oversee data management activities across our studies in solid tumors and hematological tumors. Data Management Plans, eCRF completion guidelines, Data Validation Plans, etc). Oversee internal and external database cleaning, query resolution and d...

Oversee the development and testing of clinical databases and data cleaning procedures, utilizing Medidata Rave/Veeva, and enforce data integrity through comprehensive documentation and quality control. Serve as the key data management expert on clinical project teams, guiding timelines and delivera...

Are you an experienced Clinical Data Manager with a passion for improving lives through clinical research? This is your chance to be part of an organization dedicated to delivering innovative healthcare solutions globally. Create and maintain study-specific documentation such as Data Management Plan...

This is an amazing opportunity for a data manager with strong leadership skills to lead projects and supervise a team of Clinical Data Managers. Lead and supervise Clinical Data Managers (CDMs). My client is seeking a professional with excellent communication abilities and a proven track record in c...

The Clinical Data Manager will be responsible for the clinical data management (CDM) activities for the entire life cycle of Oncology Pivotal Phase III trial(s) from protocol concept review through completion of the clinical study report. Coordinates study start-up activities; review and sign off of...

Works closely with Director of Data Management, Clinical Data Managers and Clinical Data Analyst to mentor data management staff. Serves as Project Manager on clinical studies, as needed. Oversees and manages all aspects of Data Management Operations including staffing and resourcing, project manage...

Manage Data Management tasks from study start-up to database lock for assigned studies. Minimum 10 years of experience in Clinical Data Management. Maintain study-specific documentation, including Data Management Plans, eCRF specifications, and other related documents. Coordinate with Sponsor and Ve...

Oversee, develop and maintain study-specific documentation, including Data Management Plans, eCRF specifications, CRF Completion Guidelines, Data Validation Guidelines, Data Transfer Specifications, Coding Guidelines, Post Production Database Change Control Documentation, Database Audit and Lock Pro...

Develop and maintain study-specific documentation, including Data Management Plans, eCRF specifications, CRF Completion Guidelines, Data Validation Guidelines, add Data Transfer Specifications, Coding Guidelines, Post Production Database Change Control Documentation, Database Audit and Lock Procedur...

Responsibilities Develop, build, and maintain databases of clinical trial data and establish tracking tools to track study-related data per the protocols Contribute to the development of study-specific data management processes including Statistical Analysis Plans, Data Management Plans, Case Report...

Position Summary The Manager, Clinical Data Management will lead clinical data management activities in support of CRISPR studies across all stages of clinical development. Minimum Qualifications Bachelor’s degree in a health-related field required with 7-10+ years or experience in clinical da...

Direct experience with different Data Management systems and technologies, Clinical Data Management Systems and CDISC data standards. Develop and execute data validation guidelines and measures to ensure accurate data gathering from clinical studies. Organize and direct the initial stage of the stud...

Expert knowledge of Data Management processes, efficient design/build of an EDC data management system and other Clinical Trial/Data Management Systems. Review CRO data management plans, CRF completion guidelines, edit check specifications, external data transfer specifications and other study docum...

Principal Clinical Safety Data Manager will lead and implement best practices for safety data handling, integration, reconciliation, and reporting for clinical trials. Multi-faceted background devising plans for operational challenges such as preparing data optimized for clinical data review, creati...

Responsible for reviewing the data management documentation, data management plan (DMP), CRF, study database specifications, data validation plan, edit check specifications, data transfer specifications, data issue logs, data review plans and ensures all documents follow study design and regulatory ...

Manager, Clinical Data Management. Our client is a renowned full-service clinical research organization (CRO) recognized for its expertise in clinical operations, data management, biostatistics, medical writing, and pharmacovigilance. Supervise and lead a team of Clinical Data Managers (CDMs). Offer...

Oversee the development and testing of clinical databases and data cleaning procedures, utilizing Medidata Rave/Veeva, and enforce data integrity through comprehensive documentation and quality control. Serve as the key data management expert on clinical project teams, guiding timelines and delivera...

Participate in the development of all Data Management documentation including the electronic Diary Specifications CRF, Data Management Plan, CRF Completion Guidelines, Data Validation Specification, Data Transfer Specifications, etc. Manage clinical trial data through review, cleaning, auditing, val...

Responsible for reviewing the data management documentation, data management plan (DMP), CRF, study database specifications, data validation plan, edit check specifications, data transfer specifications, data issue logs, data review plans and ensures all documents follow study design and regulatory ...

Senior Manager, Clinical Data Management in Lexington, MA with the following requirements: Master’s degree in Pharmaceutical Sciences, Pharmacology or Toxicology or related field or foreign academic equivalent plus 6 years of related experience. Prior experience must include: Develop and maintain st...

Hands-on experience with Clinical Data Management, including Case Report Form (CRF) design, CRF annotation, database design, data collection, data-entry, data validation, discrepancy management, medical coding, data extraction, database locking, and regulatory requirements. This person will be respo...

Principal Clinical Data Manager. Manage Data Management tasks from study start-up to database lock for assigned studies. Minimum 8 years of experience in Clinical Data Management. Maintain study-specific documentation, including Data Management Plans, eCRF specifications, and other related documents...