Associate Director, Clinical Data Management

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POST DATE 1/17/2020
END DATE 1/31/2020

Alexion Boston, MA

Company
Alexion
Location
Boston, MA
AJE Ref #
586384730
Job Classification
Full Time
Job Type
Regular
Company Ref #
73795744
Experience
Entry Level (0 - 2 years)
Education
High School Diploma or GED

JOB DESCRIPTION

Position Summary





The Associate Director of Global Clinical Data Management (GCDM) is responsible for directly and independently managing a subgroup of clinical data management aligned around a specific therapeutic are(s) with its associated subordinates, budgets, and schedules. The position manages all priorities and workload in the GCDM department. The position manages highly complex clinical data management projects and is responsible for clinical data management tasks to collect, code, process, review, and validate clinical trial data received in-house and remotely. The position requires the ability to manage projects and its associated teams, vendors, budgets, and timelines. The position requires activities to develop, modify, and execute company policies. Activities are performed to ensure complete, accurate, high quality, regulatory compliant data in support of publications and regulatory submissions. Activities are performed according to external regulatory requirements, and internal standard operating procedures (SOPs) and deadlines. The position is responsible for preserving data integrity and adhering to deadlines in order to ensure accurate and on-time regulatory submissions and publications.





Job Duties & Responsibilities



* Manage GCDM personnel, priorities, and workload on the preparation, validation, processing, reviewing, querying, dictionary coding, and maintenance of clinical data on individual clinical trials and regulatory submissions.

* Approve request for proposals (RFPs) for external GCDM vendor contracts. Develops and evaluates external GCDM vendor contracts and budget for project procurement.

* Manage CROs, external vendors, and clinical trial project teams.

* Implement new approved technologies and/or systems.

* Serve as subject matter expert to focus expertise and problem solving strategies on one or more of the following areas below for use across all clinical trials. Lead implementation team(s) appropriately and develop, implement, and version data standards.

* MedDRA and WHO-DD Coding – Implement centralized dictionary coding and dictionary versioning.

* Electronic Data Capture, Medidata/RAVE – Implement screen/system development; expertise on underlying data structure and data storage; manage technical system problems and take corrective action; support ad-hoc report development.

* CDASH – Implement and perform versioning; develop global standard CDASH case report form library and code lists; implement in EDC.







*

* Laboratory data standardization and collection – Define global laboratory standards library and reports; perform laboratory data review, standardization, identify data discrepancies and corresponding resolutions




* Lead the clinical project team to develop CRF/eCRF according to CDASH for clinical trials.

* Validate GCDM department to ensure audit readiness. Serve as GCDM subject matter expert on regulatory audits.

* Develop and finalize global clinical data management SOPs. Develop, modify, and execute cross-functional company policies.

* Provide training and development to GCDM personnel; prepare and conduct performance reviews. Recruits for new staff.

* Perform other activities as required.






Essential Qualifications



* Experience in clinical data management of 7-9 years.

* Possess management experience; training and development of personnel.

* Possess a thorough knowledge of medical terminology; and the clinical data management and the clinical trial process.

* Proficient on regulatory requirements for data management and the regulatory submission process.

* Experience in developing SOPs

* Experience having served as a subject matter expert on regulatory audits.

* Proficient on the design and validation of data collection instruments; the data collection and data review process; data standardization; laboratory data theory, design, and collection.

* Proficient with electronic data capture (EDC) system Medidata/RAVE.

* Proficient with the development of CRF/eCRF for clinical trials and its impact into database design/development.

* Proficient on implementing new data standards, technologies, and systems. Capable of leading implementation teams.

* Proficient on developing request for proposals for external vendor contracts, and on evaluating external vendor contract for project procurement.

* Experience in solving extremely complex and increasingly difficult problems, independently taking the appropriate corrective action, and identify and implement improvements. Able to review, interpret and evaluate clinical data.

* Possess effective written and verbal communication skills necessary to interact with personnel at all levels within and external to the company.

* Demonstrate initiative, sound judgment and flexibility; possess effective time management and organizational skills; and be able to work under deadlines and on multiple projects simultaneously.

* Able to effectively coordinate personnel, vendors, teams, and projects.

* Requires a Bachelor’s degree in a scientific discipline or equivalent.

* Competence with MS Office programs, particularly Word, Excel and PowerPoint

* Self-motivated, reliable team member

* Ability to communicate effectively with senior management as well as with peers

* Excellent written and verbal communication skills

* Good planning skills

* Ability to solve problems of challenging nature

* Adherence to timelines






Preferred Qualifications



* Proficient with: (a) CDASH, (b) MedDRA and WHO-DD dictionary coding and versioning, (c) SAS for data review.

* Obtained Certified Clinical Data Manager (CCDM) from the Society of Clinical Data Management

* A Master’s degree in a related science field is preferred.



*LI-KD1

Boston, MA, United States







Some opportunities happen only once in a lifetime - like a job where you have the extraordinary opportunity to change lives. At Alexion, such opportunities arise through our unwavering mission to serve patients and families affected by rare diseases. These patients are our guiding star, and we act with integrity, urgency, and discipline because we know their lives are at stake.





Alexion is a global biopharmaceutical company focused on serving patients and families affected by rare diseases through the discovery, development and commercialization of life-changing therapies. As the global leader in complement biology and inhibition for more than 20 years, Alexion has developed and commercializes the first and only approved complement inhibitor to treat patients with paroxysmal nocturnal hemoglobinuria (PNH), atypical hemolytic uremic syndrome (aHUS), and anti-acetylcholine receptor (AchR) antibody-positive generalized myasthenia gravis (gMG). Alexion also has two highly innovative enzyme replacement therapies for patients with life-threatening and ultra-rare metabolic disorders, hypophosphatasia (HPP) and lysosomal acid lipase deficiency (LAL-D). In addition, the company is developing two late-stage therapies, a second complement inhibitor and a copper-binding agent for Wilson disease. Alexion focuses its research efforts on novel molecules and targets in the ... To view the rest of this job posting or to apply for this position please click the APPLY NOW button