Data Management Lead

Parexel; Dover (DE); Remote; USD 110,000 - 170,000; Full time

Benefits offered by this job

Remote work (US)

Job summary

Parexel is seeking a remote-based Data Manager Lead / Data Manager II to join our global Data Management team. You will provide technical leadership across all data management activities, manage study data delivery timelines, and serve as the primary DM contact for assigned studies.

You will mentor junior staff, collaborate with Clinical, Biostatistics, Programming, Medical Writing, and cross-functional teams across time zones, ensure inspection-ready TMFs, and drive QA compliance and sponsor

Qualifications

• Strong hands-on Data Management experience in clinical research.
• 6+ years of data management experience across studies and phases.
• Experience with DM systems (Rave/InForm) and regulatory standards.

Responsibilities

• Lead cross-functional Data Management activities across global teams.
• Manage study data delivery timelines, Go-Live, and database lock.
• Ensure quality, timeliness, and inspection readiness of DM deliverables.
• Mentor Assistant Data Managers and peers as needed.
• Support audits, CAPAs, and sponsor metrics.

Skills

Global team leadership

Negotiation

Communication

Learning agility

Time management

Ownership & accountability

Travel ability

English fluency

Problem solving

Education

Bachelor's degree in science or related field

Tools

Medidata Rave

InForm

Veeva

DataLabs

Microsoft Excel

CDISC/SDTM knowledge

Job description

We are hiring a remote based Data Manager Lead / Data Manager II to join our Parexel team.

Location: Continental US

About the Role

The Data Manager Lead / Data Manager II provides technical expertise across all aspects of Data Management and serves as the primary Data Management point of contact for assigned studies. This role is responsible for ensuring contracted Data Management deliverables are met with a focus on quality and timeliness, while collaborating closely with cross-functional teams across global geographies.

The successful candidate will manage study data delivery timelines, including Go-Live, Interim Deliveries, and Final Database Lock, while working with minimal guidance from Line Managers and/or Subject Matter Experts. The Data Manager II may also provide mentorship to Assistant Data Managers and Data Management peers.

Key Responsibilities

Cross-Functional Data Management Leadership

• Manage study data delivery timelines, including Go-Live, Interim Deliveries, and Final Database Lock.

• Collaborate with Clinical, Biostatistics, Database Programming, Medical, Medical Writing, and other cross-functional stakeholders across global regions.

• Manage and coordinate the integration and utilization of ancillary systems, as appropriate.

• Identify risks and issues impacting study delivery, define mitigation strategies, and drive issue resolution with stakeholders.

• Review and analyze study metrics to identify trends and summarize study health.

• Review Master Services Agreements, Service Level Agreements, and contracts to manage sponsor-specific metrics and Key Performance Indicators.

• Attend cross-functional meetings and prepare agendas, meeting minutes, action logs, and decision logs.

Bid Pursuits and Proposals

• Demonstrate technical and operational Data Management expertise and capabilities tailored to sponsor needs.

• Provide input for bid pursuit presentations and materials.

• Effectively represent the Data Management function as part of a cross-functional team during sponsor presentations.

Quality Management and Compliance

• Ensure compliance with Standard Operating Procedures and ICH/GCP guidelines.

• Maintain inspection-ready Trial Master Files.

• Identify and document quality issues, ensuring appropriate resolution and closure.

• Prepare for and participate in internal, sponsor, and regulatory audits and inspections.

• Drive and implement corrective and preventive actions and share lessons learned across projects and programs where appropriate.

Financial and Resource Management

• Collaborate with Delivery Leads and line management to ensure appropriate project resourcing and staff assignments.

• Identify and request functional resources required for project delivery.

• Support the resolution of Data Management-related project variances, including scope changes where applicable.

Company Initiatives

• Provide Data Management input to organizational initiatives.

• Collaborate with cross-functional stakeholders to provide meaningful feedback on initiatives.

• Ensure information maintained in management systems is accurate and up to date.

Training and Development

• Maintain required training compliance, including on-the-job training.

• Deliver project-specific training to internal Data Management teams.

• Support identified development goals and training needs.

• Provide on-the-job training when needed.

Required Skills

• Strong ability to lead and collaborate with global teams across multiple time zones and cultures.

• End to Strong negotiation and influencing skills.

• Excellent interpersonal, written, and verbal communication skills.

• Strong learning agility and knowledge-sharing mindset.

• Flexibility and adaptability in changing environments.

• Effective presentation skills.

• Strong customer focus with the ability to build rapport and trust.

• Commitment to quality with a methodical and accurate approach to work.

• Strong time management and prioritization skills.

• Proven problem-solving and root cause analysis capabilities.

• Strong sense of ownership and accountability.

• Ability to travel as required.

• Written and spoken fluency in English.

Knowledge and Experience

• Strong experience within the clinical research industry.

• 6+ years of hands on Clinical Data Management experience

• Hands-on Data Management expertise across all phases (startup, conduct, closeout)

• Experience authoring/coauthoring standard Data Management documents

• Hands on experience working in Medidata Rave

• Proven experience leading project and program teams.

• Good understanding of project tools, reports, and processes related to project financial management, including forecasting, revenue recognition, scope of work, and departmental budgets.

• Good understanding of Clinical Study Team roles outside of Data Management.

• Strong knowledge and application of ICH-GCP guidelines, local regulatory requirements, Standard Operating Procedures, and study-specific procedures.

• Awareness of SDTM, CDISC, and CDASH standards.

• Strong technical proficiency with Clinical Trial/Data Management Systems such as InForm, Rave, Veeva, DataLabs, and Microsoft Office applications.

Education

• Bachelor’s degree and/or other qualifications in a science or clinical-related field.

#LI-REMOTE

EEO Disclaimer

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.