The Project Data Manager (PDM) leads and oversees data management activities, timelines and finances of the Allucent Data Management (DM) department.
This position manages and coordinates DM deliverables from database design & set-up, through cleaning and reporting to database locking, ensuring that the completeness, accuracy and consistency of clinical data meets the quality standards and regulatory requirements for analysis and reporting.
This position acts as a Project Manager and is responsible for the overall coordination and management of Data Management/Biostats standalone projects, large and complex trials and/or multiple projects belonging to one client.
This position oversees day-to-day operations and coordinates planning and operational activities of assigned junior team members, like, CDM1, CDM2 and CDM3 and their assigned projects.
The PDM is a member of the Data Management staff.
Requirements
· Lead and serve as primary contact for DM with all relevant parties both internally (e.g. Biostatistics and if applicable other functional groups, such as Project Management, Clinical Operations) and externally (e.g. sponsors, vendors (EDC, external data), investigational sites)
As a Project Manager for Biometrics stand-alone studies, the Project Data Manager will:
· Lead and coordinate the Biometrics project team, ensuring the project is delivered according to planned scope and timelines in accordance with the contract
· Create and execute project management plans required for project delivery and in accordance with established processes
· Establish requirements for and ensure project-specific training plan for internal team members
· Establish clear communication lines and escalation pathways, communicate with project stakeholders, both internally (e.g. Clinical Programmers, Data Scientists, Biostatistics and other functional groups) and externally (e.g. sponsors, vendors (EDC, external data) and other external parties)
· Establish requirements for and ensures project-specific training plan for internal team members
· Lead and serve as primary contact for DM with all relevant parties both internally (e.g. Biostatistics and if applicable other functional groups, such as Project Management, Clinical Operations) and externally (e.g. sponsors, vendors (EDC, external data), investigational sites)
As a Project Manager for Biometrics stand-alone studies, the Project Data Manager will:
· Lead and coordinate the Biometrics project team, ensuring the project is delivered according to planned scope and timelines in accordance with the contract
· Create and execute project management plans required for project delivery and in accordance with established processes
· Establish requirements for and ensure project-specific training plan for internal team members
· Establish clear communication lines and escalation pathways, communicate with project stakeholders, both internally (e.g. Clinical Programmers, Data Scientists, Biostatistics and other functional groups) and externally (e.g. sponsors, vendors (EDC, external data) and other external parties)
· Establish requirements for and ensures project-specific training plan for internal team members
· Establish project risk management plan with input from client and functional stakeholders and oversee adherence and updates throughout the project lifecycle
· Lead internal meetings with internal team members and external meetings with a sponsor, and third party (data) vendors, including Kick Off Meetings (KOM) and Investigator Meetings based on project scope
· Provide support for vendor identification, qualification and selection and manage vendors
· Manage vendors and vendor relationships as required for project delivery
· Arrange, maintain and circulate project progress and status reports
In addition, as a Project Manager for Biometrics stand-alone studies and/or large, complex or multiple studies with same client, the Project Data Manager will:
· Lead the Biometrics project team, ensuring the project is delivered according to planned scope and timelines in accordance with the contract
· Ensure overall consistency across all client studies within a set of projects; this especially relates to the DM activities; Data Management Plan (DMP), CRF design, data cleaning and query management) and for Biometrics stand-alone projects also include statistical deliverables (SAP, TLFs)
· Lead internal meetings with internal project team members. Support and participate in external meetings with a sponsor, including Kick Off Meetings (KOM) and Investigator Meetings based on project scope
· Interact, negotiate and influence internal and external team members in a professional manner and with successful outcomes
· Ensure effective and efficient resource utilization across projects and programs
· Manage the study budget, evaluate financial project health and manage monthly status updates for invoicing. Participate in monthly project review meetings
· Proactively recognize and address any changes in scope. Liaise to execute contract amendments
· Oversee Sponsor relationships
· Assist in contracts negotiation and contracting process with vendors (EDC, IRT)
· May support operational Data Management activities, also to ensure and assess quality
· Oversee and ensure the Trial Master File for DM services in scope is kept up to date and audit/inspection ready.
· Contribute to other areas of business as required
· Research, propose and lead initiatives for improving efficiency
· Manage direct reporting staff, perform performance reviews and support team member personal development plans
· Oversee and supervise work done by junior team members (CDM1 level – CDM3 level)
· Actively support to staff learning & development within the company
· Share relevant information at applicable DM departmental meetings and organize and lead DM-related meetings and discussions
· Represent the company through active participation at professional meetings, webinars or seminars
· Provide and coordinate Data Management training for relevant staff. Support in development of new training material
· Train and mentor data management staff, support in development of new training material and provide training to relevant staff
· Participate in the interview process for new recruits
· Proactively track Data Management related regulatory development trends and updates, in consultation with department Global Head and/or Senior Directors, for further alignment and improvement of current processes
Quality Management
· Contribute as Clinical Data Management Subject Matter Expert (SME) to the evaluation/improvement/drafting of processes and procedures within the Quality Management System
Account Management, Sales & Acquisition
· Assure good communication and relationships with (future) clients
· Contribute to and take part in client evaluations and visits
· Support in preparation of new proposals and budgets for Data Management services
· Support Business Development (BD) in preparing and providing presentations to potential and existing clients through attendance at capabilities and/or bid defense meetings
· Provide input into tools and templates to support costing and bidding
Others
· Contribute to other areas of business as required
· 10% Travel
Education Requirements and Qualifications
· Life science, healthcare degree and/or combination of education and experience
· Minimum 8 years of relevant work experience in Clinical Data Management or related experience within Biometrics
· Minimum 8 years of relevant experience in related clinical trials environment
· Thorough knowledge and understanding of ICH-GCP, 21CFR11 data privacy (GDPR/HIPPA) guidelines and awareness of local/regional requirements
· Good understanding of Medical Terminology
· Experience as DM Lead on several studies and experience in covering all phases of a clinical study (start up, conduct and database lock). Worked on multiple indications and clinical phases (I-IV)
· Thorough understanding of relational database components and experience in technical data management practices (validation plans, testing, and documentation
· Experienced in CDISC conventions, i.e., CDASH, TAUG models and hands on experience implementing these models
· Client management experience
· Experience in developing data management standards
Skills
· Strong written and verbal communication skills including good command of English language
· Representative, outgoing and client focused
· Ability to work in a fast-paced challenging environment of a growing company
· Proficiency with various computer applications such as Word, Excel, and PowerPoint required
· Administrative excellence
· Attention to detail, strong technical, analytical and problem-solving skills
· Strong project management skills
· Ability to translate guidelines, rules and regulations in clear and usable recommendations
· Ability to simplify complex issues into understandable concepts
· Excellent organizational, negotiating and motivational skills
Benefits
Benefits of working at Allucent include:
Disclaimers:
“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”
Allucent Clinical Research Organization™ is on a mission to help bring new therapies to light by solving the distinct challenges of small and mid-sized biotech companies. We’re a global provider of comprehensive drug development solutions, including consulting, clinical operations, biometrics, and clinical pharmacology across a variety of therapeutic areas. With more than 30 years of experience in over 60 countries, our individualized partnership approach provides experience-driven insights and expertise to assist clients in successfully navigating the complexities of delivering novel treatments to patients. Allucent nurtures a high-performance culture in which we provide continuous training and put emphasis on personal and organizational development and opportunities, anchored by a commitment to high-quality and personalized customer service. We consider effective, frequent, and open communication a key component of developing strategies to meet your needs and goals. We provide lean project management to accomplish operational excellence in terms of timelines, quality, and costs.
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