Clin Data Assoc II

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.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.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.