16 days old

Data Acquisition Analyst, Clinical Data Acquisition

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--Provide technical solution in assigned functional areas, including but not limited to: Vendor Qualification Assessment, Data transfer specifications creation, Test Data Review, Data review model creation and Data loading monitoring, LNMT setup

--Accountable of on time delivery in assigned function areas with high quality

Identify, lead and support strategic initiatives within DMM to enhance operational efficiencies using systems and systems enabled processes.

--Collaborate with other Data Acquisition Analysts to develop and maintain a support model and to facilitate issue resolution and capture corrective actions; and to ensure operational efficiencies such as sharing of best practices across work areas, functions and sites.

--Implement global strategies, initiatives, processes, and standards to ensure consistent, efficient, and quality processes to meet quality, timelines and deliverables.

--Plan and execute communication plans & methods to ensure customer satisfaction and enable improvements to be implemented during the course of a study.

Improve and maintain customer satisfactory level in the function areas

--Able to resolve conflicts, influence and communicate with key stakeholders and customers.

--Provide technical expertise and business process support in systems supporting clinical trials, e.g. in DMW input model creation and validation

--Thorough understanding of the processes associated with clinical study management, data management, and regulatory operations

--Leadership, project management, administrative, and technical capabilities are expected, as well as effective verbal and written communication skills in relating to colleagues and associates both internal and external to the organization.

--Demonstrated project management skills


--Demonstrated knowledge of clinical development process including knowledge and understanding of the principles of GCP

--Demonstrated knowledge of data management processes and principles in area of responsibility.

--Working knowledge of all phases of clinical trials and ability to assess and determine study requirement from protocol review

--Demonstrates strong verbal and written communication skills including ability to communicate remotely

--1-3 years Data Management experience required

--Working knowledge of clinical research, FDA & ICH, GCP, GCDMP, and related regulatory requirements

--Proficient experience using commercial clinical data management systems and/or EDC products (e.g. , Inform preferred)

--Experience using data visualization tools (e.g. Spotfire, J-Review) preferred

--Familiarity with MedDRA/WHO-Drug

--Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)

--Bachelor's degree minimum requirement.


Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Posted: 2020-10-13 Expires: 2020-11-13
Sponsored by:
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