PPD is a leading global contract research organization providing discovery, development and post-approval services as well as compound partnering programs. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 32 countries and more than 9,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a commitment to quality to help its clients and partners maximize returns on their R&D investments and accelerate the delivery of safe and effective therapeutics to patients.
Post : Clin Data Assoc II
Job Description
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.
Candidate Profile
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 grid Ability 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 numbers Ability to use interactive computer programs Good written and verbal communication skills Good organizational skills Good analytical/problem-solving skills Ability to work productively with moderate supervision Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data Ability to attain, maintain and apply a working knowledge of Good Clinical Practices and applicable Standard Operating Procedures Strong customer focus and excellent interpersonal 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 trial terminology PPD 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
Additional Information
Experience : Minimum of 6-12 months
Qualification : B.Pharm, B.Sc, M.Sc
Location : Bengaluru
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Clinical Data
End Date : 25th October, 2019
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