29 days old

Mgr Clinical Data Solutions

USA - 2778 Millennium Pharmaceuticals, Inc.
Boston, MA 02109
  • Job Code
    R0021594

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Job Description

Position Title: Manager, Clinical Data Solutions

OBJECTIVES:

Responsible for timely and high quality data management deliverables supporting the Takeda portfolio.

Confirms asset and study level strategies and services are being implemented at the study level, including the application of standards.

Conducts oversight of data management activities performed by Strategic Partners and/or other CROs and other 3rd party vendors to meet Takedas obligations described in ICH-GCP and Takedas business objectives. Activities include from protocol synopsis through database release and submission

Contributes to the management of vendor partnerships to verify contractual assumptions in the study SOWs including the verification of monthly invoices.

Acts as a first point of contact for CRO partners seeking sponsor input on study level problem solving and decision making.

Serves as an expert for clinical data management best practices and acts as an ambassador on CDISC standards.

ACCOUNTABILITIES:

Participates in study level vendor oversight activities. May represents data management function on the Clinical Sub-team ensuring aligned expectations between the CRO and

Takeda for all data related deliverables, especially in support of key decision points and regulatory submissions.

Serves as a first point of contact for CROs partners when collaboration is needed to ensure established milestones and deliverables are met with the highest degree of quality.

Partners with appropriate stakeholders and CRO partners to mitigate and resolve risks. Acts as a process expert for operational and oversight models.

Maintains SOPs, process maps and templates and timelines to support functions operational and oversight models.

May prepare metrics to support the functions KPIs.

Tracks study deliverables and evaluates study metrics to mitigate risk for major data management deliverables and milestones.

Confirms archival and inspection readiness of all Data Management Trial Master File (TMF) documents Verifies external Data Management SOWs and timelines to ensure accuracy of invoices, investigates variances and supports forecasting.

Participates in preparing function for submission readiness and may represent function in a formal inspection or audit. Other duties as assigned

EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:

BS/BA required preferably in a health-related, life science area and with a minimum of 6 years data management and/or drug development experience.

Proven track record of strong project management skills and experience managing data management activities for large drug development programs

Experience with all phases of development and at least 2 therapeutic areas.

Ability to handle multiple development programs simultaneously.

NDA/CTD Experience.

Strong knowledge of electronic data capture and data warehouse technologies as applied to clinical trials.

Strong working knowledge of (e)CRF design and data management functions/activities as applied to standards library development and maintenance.

Good understanding of CDISC standards, and experience implementing standards.

Strong knowledge of clinical study reporting requirements including SAS programming.

Advanced knowledge of office software (Microsoft Office).

Solid understanding of clinical trial documents (protocols, statistical analysis plans, CRFs, study reports) and processes.

Advanced knowledge of FDA and ICH regulations and industry standards and quality control principles.

Experience in medical coding in the pharmaceutical/biotechnology industry including knowledge of coding tools.

Good working knowledge of general statistical programming processes and practices. Advanced knowledge of medical terminology, medical coding, laboratory reference ranges, clinical diagnostic procedures, anatomy/physiology and nature of disease processes. Demonstrated strong matrix leadership and communication skills

Able to influence without authority

Excellent teamwork, organizational, interpersonal, conflict resolution and problem-solving skills

Entrepreneurial and innovative; takes measured risks; thinks outside the box; challenge the status quo

Pragmatic and support change Is comfortable with ambiguity

Locations

Boston, MA

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time





Posted: 2020-07-17 Expires: 2020-08-15
Sponsored by:
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Sponsored by:
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Mgr Clinical Data Solutions

USA - 2778 Millennium Pharmaceuticals, Inc.
Boston, MA 02109

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