PPD looking for Clinical Data Associate,
The objective of a
Clinical Data Associate II is to perform advanced aspects of the data cleaning
process with a high level of accuracy and in accordance with Good Clinical
Practices and Standard Operating Procedures/Working Practice Documents, in
order to assess the safety and efficacy of investigational products and/or
medical devices.
Clinical Data
Associate II's are expected to perform the tasks of a Clinical Data Associate I
with increased efficiency, while maintaining a high level of accuracy, and to
work more independently. In addition
they will be expected to perform data management activities such as Serious
Adverse Event and Third Party Vendor reconciliations as well as Data Listing
reviews.
Education and
Experience:Bachelor's degree or certification in a related allied health
profession from an appropriately accredited institution (i.e. RN, MT, PA, RPh,
RT)Minimum of 6-12 months experience in data management In some cases, a
demonstration of applicable technical and behavioral competencies, and a combination
of education and prior directly related experience may be considered as
equivalent to the above requirements provided that the individual possesses the
following knowledge, skills, and abilities to perform the job requirements
satisfactorily Knowledge, Skills and Abilities:Proven ability in achieving
applicable technical competencies per the CDM competency gridAbility to
effectively apply knowledge and skills in a highly organized fashion while
adhering to regulatory guidelines, global Standard Operating Procedures and
client expectations Strong attention to detail and skill with numbersAbility to
use interactive computer programsGood written and verbal communication
skillsGood organizational skillsGood analytical/problem-solving skillsAbility
to work productively with moderate supervisionAbility to maintain a high degree
of confidentiality with clinical data and client's proprietary dataAbility to
attain, maintain and apply a working knowledge of Good Clinical Practices and
applicable Standard Operating ProceduresStrong customer focus and excellent
interpersonal skillsProven flexibility and adaptabilityAbility to work in a
team environment and independently as neededMust demonstrate good judgment in
making decisions Must be able to set and meet timelines or be able to negotiate
schedule changes in response to project demandsStrong command of English
language and grammarKnowledge of medical/clinical trial terminologyPPD is an
equal opportunity employer (EOE) that will not discriminate in its employment practices
due to an applicant’s race, color, religion, sex, national origin, and veteran
or disability status by embracing diversity and the responsibilities of
corporate citizenship in our communities. PPD values our former military and
transitioning service member’s service.
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