IQVIA Lead/Senior Lead/Principal Clinical Data Manager (Home/Office-Based) - IQVIA Biotech in Waltham, Massachusetts
IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.
In anticipation of future growth, IB is proactively seeking to identify Data Managers with Lead experience.
POSITION TITLE: Senior Lead Clinical Data Manager
REPORTS TO: Manager or Director-level Data Management or Designee
Senior Lead Clinical Data Manager position is to manage all data management (DM) tasks to include more complex and/or larger studies and/or a program of studies from start-up through database closure and archival producing high-quality databases for analysis and potential regulatory submissions.
ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:
Manages DM-related aspects of the program and/or project
Collaborates with the project team on overall data management strategy for the program and/or projects, assuring overall quality and efficiency
Represent DM as the functional lead at internal and sponsor project team meetings
Provides proactive, timely communication of project status, data trends and issue resolution with internal team and Sponsor
Develops, generates and analyzes project progress and/or metric reports, reporting summary of findings and remediation activities, as required, to DM management, project team and Sponsor
Assumes ownership for DM project deliverables within DM scope of services including creation and management of DM-specific timelines and providing resource and budget projections
Discusses roadblocks to DM deliverables and potential strategies for overcoming with project team and/or DM management and implements solutions
Performs peer reviews of key DM study documents or other DM deliverables to assure quality of content and, where appropriate, consistency across a program of studies
Reviews and provides DM staffing projections for program and/or projects
Presents EDC and/or CRF completion at Investigator Meetings
Participates in regulatory and Sponsor audits for program and/or projects
Oversees daily team member activities
Serves as a Data Management team leader
Reviews DM team member activities and deliverables to ensure plans and processes are followed
Assures project activities are performed within budget and according to expected timelines and meet high quality standards.
Reviews resource allocation with the assigned DM project leads to ensure projects and budgets are managed effectively
Provides training of DM staff on project specific processes
Oversees the DM project and/or program team and performs DM tasks, as required, based on the approved Data Management and Data Review Plans including but not limited to:
Data Reconciliation (e.g., Vendor, SAE) including coordination of transfers and issue resolution with other functional areas and/or 3rd party vendors
Investigation and remediation of reviewer-reported data issues such as from statistical, medical or Sponsor reviews
Assumes ownership for DM project deliverables within DM scope of services including overseeing overall quality, adherence to Study Plans and standard operating procedures, coordinating with manager for resourcing requirements
Oversees System Development and Modifications:
Implements DM strategy on the project/program based on scope of services and as laid out by DM management
Coordinates with Technical Design and Clinical Programming team as well as Project Management to develop and maintain DM startup timelines including the development, testing and implementation of all data capture tools
Coordinates with vendors and cross-functional teams to assure timely completion of tasks to meet established timelines
Coordinates with the Technical Design and Clinical Programming team and/or 3rd party vendor to develop and test the CRF and edit check specifications as well as custom EDC reports to support protocol requirements
Coordinates with the EDC programmers and/or 3rd party vendors in the setup and testing of electronic data capture (EDC) technologies such as Interactive Response Technology (IRT), electronic patient reported outcomes (ePRO), and electronic clinical reported outcomes (eCOA) as required per the scope of work.
Facilitates project team and Sponsor reviews of system documents including but not limited to Time and Events Schedule, CRFs, Edit Checks, revision specifications
Consolidates reviewer comments from internal team/sponsor and collaborates with the project and Clinical Programming team, as required, for revisions
Coordinates with the project team as well as the Technical Design and Clinical programming team to manage post go-live EDC modifications assuring effective implementation (including consistency across program when applicable) and team communication for program and/or projects
Oversees System and Data Listing Testing Activities:
Coordinates testing activities for the EDC technologies per scope of services
Performs testing for EDC systems as required per scope of services and standard operating procedures
Verifies reports created in EDC or other ad hoc reporting tool like J-Review, BOXI and associated change control requests
Provides feedback to the other project team members and managers to improve the deliverables.
Develops, Maintains and Archives DM Project Documentation including:
Data Management Plan, Data Review Plan, CRF Completion Guidelines. and other study-specific plans as required
Data review listing specifications
Database Design Documents, Edit Specifications, Reconciliation guidelines, and Report specifications
Database lock documentation
Represents Data Management at Bid Defense Meetings (BDM)
Prepares project-specific slide presentation from DM template functional slides
Participates in BDM preparation meetings including discussing overall DM strategy
Presents DM slides at BDM and constructively participates in discussion
Recommends and assists in the development of standards and/or improvements to existing standards including processes, CRFs, data listing reports and document templates
Serves as Data Operations mentor
Creates and maintain documentation for templates (DMP, CRF Completion guidelines, Database Design Documents, Edit specifications, Reconciliation guidelines, Report specifications)
Trains others on specific departmental processes including database design document creation, edit check creation, change control processes, database lock
Provides open environment for question/issues about DM topics from within department and cross-functionally
KNOWLEDGE, SKILLS AND ABILITIES:
Team player with ability to learn new skills, tasks and technologies and teach others
Ability to collaborate and strategize with both technical and clinical team members (CRAs, Safety, Biostatistics, etc)
Ability to effectively communicate technical issues to non-DM team members and Sponsor
Ability to maintain positive and open relations with internal, sponsor, and vendor team members
Ability to facilitate team meetings ensuring accurate attendees and take meeting minutes
Ability to develop study-specific procedures
Knowledge of clinical trials concepts
Ability to create detailed DM project instructions and documents (CRF Completion Guidelines, Database design documents, edit check specifications, Data Review Plan, etc.)
Proficiency with multiple clinical EDC systems (preferred systems are InForm and Rave)
Proficiency with IQVIA Biotech SOPs, WPs
Efficient with organizational skills to meet established timelines
Organized and thorough with attention to details
Excellent verbal, written and listening communications skills
Effective interpersonal skills including ability to provide and accept constructive feedback
Effective logical thinking ability regarding problem-solving skills
Proficiency in computer applications and time management tools (e.g., MS Office)
CRITICAL JOB FUNCTIONS IN ACCORDANCE WITH ADA CRITERIA:
Very little physical effort required to perform normal job duties (unless otherwise indicated)
Occasional travel for Bid Defense Meetings, Investigator Meetings, client face-to-face meetings, user group meetings or training courses. Travel not anticipated to exceed 2-3 times per quarter.
MINIMUM RECRUITMENT STANDARDS:
Bachelor’s degree, or educational equivalent, in clinical, biological or mathematical sciences, or related field, or nursing qualification
7 years of experience in clinical trials within a similar function, including:
proven competence in managing delivery of multiple projects / programs independently through full data management study life-cycle
experience in handling bid defense meetings
Equivalent combination of education, training and experience
This position is classified as exempt under the Fair Labor Standards Act; employees are not eligible for overtime compensation.
Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.
Forge a career with greater purpose, make an impact, and never stop learning.
IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled
IQVIA, Inc. provides reasonable accommodations for applicants with disabilities. Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA’s Talent Acquisition team at email@example.com_ to arrange for such an accommodation.
At IQVIA, we have a vision. Where every healthcare decision is based on evidence. Where data science and human science come together to improve global health. Where new and creative solutions aren’t just possible – they are expected.
Thank you for your interest in growing your career with us. It takes insight, curiosity, and intellectual courage to transform healthcare. The 56,000+ employees of the IQVIA family of companies, including Q2 Solutions, are reimagining a world without the consequences of disease. We are brave minds bringing powerful ideas to reality. At IQVIA, you can truly make an impact in an environment where you’re supported to succeed.
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