The objective of a Clinical Data Associate is to perform all aspects of the data cleaningprocess, with minimal supervision, in accordance with GCPs and SOPs / WPDs to assess thesafety and efficacy of investigational products and / or medical devices.
Clinical DataAssociates are expected to perform the tasks of a Clinical Data Associate I with increasedefficiency, while maintaining a high level of accuracy, and to work independently.
In addition,Clinical Data Associates may begin to perform data management activities such as CRFdesign, database design, and DVM creation in conjunction with Lead Data Manager trainingprogram.
May provide training and work direction to junior staff as requiredFunctions
Considering 0-1year of experience
In some cases, a demonstration of applicable technical and behavioural 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.
Bachelor’s degree OR certification in a related allied health profession from an appropriatelyaccredited institution (i.
e. RN, MT, PA, RPh, RT).Knowledge, Skills and Abilities :
Proven ability in achieving applicable technical competencies per the CDM
Ability to effectively apply knowledge and skills in a highly organized fashion while
adhering to regulatory guidelines, global SOPs and client expectations.
Strong attention to detail and skill with numbers.
Ability to use interactive computer programs.
Good written and verbal communication skills.
Proven flexibility and adaptability.
Ability to work in a team environment and independently as needed.
Must 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 demands.
Strong command of English language and grammar.
Knowledge of medical / clinical terminology.