Lead Data Manager for Clinical Trials

Sobre esta vaga

The Lead Data Manager will be responsible for all data management activities in large, complex studies under general supervision, or working under minimal supervision on data management activities for small to medium sized projects. Communication

Primary communication point for project teams and company departments with regard to clinical data management

Communication line for clients/vendors for all data management aspects of clinical projects and clinical data management reporting

Data Management

Coordination of data management activities within clinical projects related to EDC development, data collection, cleaning, reconciliation, Database Lock, development of final integrated database and generation of final Data Management deliverables.

Primary responsibility for clinical data management activities within clinical projects, including, but not limited to: Study documents review

Data Management plan and other project-specific guidelines and instructions development and review

Co-ordinate/perform user acceptance testing

Development of Data Validation Plan/Edit Check Specifications

Data entry coordination and supervision, feedback to data entry personnel regarding quality of data entry and other data entry issues

Data validation, including automatic and manual data inspections, data discrepancies/deficiencies review and resolution, query generation and resolution, feedback to clinical trial teams regarding quality of data

Non-CRF electronic data handling (receiving, archiving, loading into study database, review and resolution of reconciliation issues, feedback to vendors regarding quality of data and other issues)

Database edits (paper CRF studies)

Manual CRF review (non-medical checks)

Clinical database lock

Coordination and supervision of processing, dispatch and archiving of CRFs/queries

Input into design of CRFs and other data collection forms; review Case Report Form design for accuracy and adherence to protocol

Development of CRF completion guidelines

Coding medical data with coding dictionaries and coding listings review (Lead DMs with medical/biology background, additional training required)

SAE reconciliation

Electronic data transfer (import/export) specifications review and approval

Document Management Liaison with Document Center with regard to maintenance of TMF and eTMF Quality Control

Database QC checks performance and documentation

Shared responsibility for preparation and attendance at internal and client/third-party audits/inspections of Data Management

Shared responsibility for follow-up on and resolution of audit findings pertaining to Data Management

Training

Training of Assistant Data Managers

Project-specific training of investigators and clinical team in CRF completion

Corporate/Departmental Assignments

Investigator Meetings preparation/attendance

Meetings and teleconferences organized by client/vendor preparation/attendance

College or University degree or equivalent combination of training and experience that presents the required knowledge, skills and abilities

At least 3 years of experience of full scope of data management responsibilities in international EDC studies

At least 2 years of experience using CDM/EDC systems (Medidata Rave or Oracle Inform preferable)

Project data management experience is a plus

Full working proficiency in English

Organizational and managerial skills

Advance your career in clinical research and develop new skillsets whilst growing with the organization. We’re over 2,700+ strong across the globe. We’re scientists, strategists, creatives, and innovators. We value individual brilliance and build a strong foundation for teamwork across all our business. We love the challenge of our industry. We’re changing lives and redefining success every step of the way. Originally posted on Himalayas