Senior/Principal Data Manager

Alira Health•Boston, MA

About The Position

ROLE The Senior Data Manager e nsure s DM tasks for the assigned studies are performed on time and within budget , p artner s with Sponsors, clinical and statistics to develop the data collection specification from all data sources The Senior Data Manager m anage s in-stream data flow activities and deliver a quality database in accordance with the project plan , l ead s and drive the DM team , and a ct s as the reference point for the Sponsor and the appointed person responsible for the project from the data management perspective .

Requirements

Recent experience in using Medrio as Study Data Manager and CRF building
Degree in life science, pharmaceutical, biology or related field or at least 3 years’ experience in data management field or similar in a pharmaceutical environment or equivalent
Knowledge of Data Management processes, Good Knowledge of pharmaceutical industry guidelines like ICH, GCP etc , Good Knowledge of coding dictionaries like MedDRA and WHO-DD or equivalent, Good Knowledge in one or more DM systems, Good
English, Good
MS Office Suite, Good
Professional
Trustworthy
Ability to effectively prioritize
Quality focused
Personable
Attitude
Willingness to learn
Team Player
Effective Stress Management Techniques
Learning Agility
Ability to Manage Conflict
Problem Solving Skills
Effective Verbal Communication Skills
Commercial and Technical Writing Skills
Networking Skills

Responsibilities

Accountable for driving achievements of project milestones from study start up through to delivery of database
Provide Data Management input into the protocol
Design the Case Record Form and guide process for CRF approval
Define and develop the Data Management Plan, Data Validation Plan and their annexes ( e.g. Reconciliation Plan), with input from the study team
Validation of the database and computerized checks, including SAS listings or SAS checks
For EDC studies, define the User Acceptance Test Plan (UAT) and execute the test activities in the test environment to ensure quality eCRF
For EDC studies timely response to issues identified by the eCRF Helpdesk
Prepare CRF completion guidelines
Prepare study specific data-entry guidelines and train data-entry staff
Perform term coding for clinical studies, raise manual queries for uncoded terms as Query management: review discrepancies, review answered queries, resolve and close where appropriate , manage the data cleaning process including manual checks and Medical Review listings
Create and test import programs for electronic data received from external vendors
Perform timely data integration of CRF and non CRF data (data import from external sources)
Perform reconciliation of external data ( e.g. SAE, Central Labs, ECGs, etc )
Run and monitor study data progress reports including query management and take appropriate actions ( e.g. escalation, re-training, etc ), escalate any study issues within study team
Define and execute QC plan, lead and execute database release and database freeze activities
Lead the DM team, coordinate other DM staff providing direction regarding work assignment, scheduling and prioritizing
Input into and monitor progress against study project plan and escalate issues to resolution at the appropriate level
Effectively contribute in formal training for new starters
Demonstrate good application of document management process and procedures
Follow SOPs and guidance documents as well as applicable industry standards like ICH, GCP etc to day-to-day activities
Make recommendations for process improvements and development of new standards
Develop and maintain a network of contacts within the study team
Lead the DM team, coordinate other DM staff providing direction regarding work assignment, scheduling and prioritizing; monitor progress of activities
Maintain continuous and appropriate communication with sponsor and share with them critical and general issues
Effectively represents Data Management in internal or external meetings ( e.g. Investigator’s Meetings)
Conduct other activities as