Clinical Data Manager II - UK, Spain, Ireland - €3000 Sign-on Bonus

PPD Europe ,
London, Greater London
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Overview

Company description: PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 48 countries and over 23,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to help clients and partners bend the cost and time curve of drug development to deliver life-changing therapies that improve health. Job description: PPD is seeking an experienced Clinical Data Manager to join our global Data Management department. For a limited period, PPD is offering a Sign-On Bonus of €3000 to candidates who are hired. This is a full-time position, and we can offer home or office based opportunities. The objective of a Clinical Data Manager (CDM) is to act as a lead data manager for one or more projects. CDMs may lead multiple, high volume/highly complex studies. In this role, you will independently lead and/or efficiently perform, with quality, all data management activities within an assigned study. You may mentor junior level staff on all associated tasks within a study. The role also involves liaising with the sponsor as required and communicate with management regarding all data management activities within your studies. You may also participate in business development activities as required. Required profile: Education and Experience: Bachelor's degree or equivalency in education (e.g., R.N., M.T., P.A., R.Ph, etc.) and experience demonstrating theoretical knowledge of biology, chemistry, physics, and/or health sciences, or closely related 3 years of data management experience Or a combination of performance, 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: Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, Standard Operating Procedures and client expectations Strong attention to detail and skill with numbers Good written and verbal communication skills Good organizational skills Good analytical/problem-solving skills Ability to work productively with minimal 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 Ability to act as a study or department expert for DM processes Ability to assist in forecasting project resourcing and hours needed Ability to train and direct study team Must demonstrate good judgment in making decisions Ability to travel to other locations as required or as business need dictates Must be able to set and meet timelines or be able to recognize and schedule changes in response to project demands Ability to identify potential out of scope activities to project and CDM management and to assist with the contract modification process Strong command of English language and grammar What we offer: If you are passionate about your work, and want to apply and develop your skills, PPD provides rewarding career opportunities in a variety of fields. Individuals who are motivated and enthusiastic team players thrive at PPD and ultimately help our clients accelerate the delivery of safe and effective therapeutics for some of the world’s most urgent health needs. This job was originally posted as www.totaljobs.com/job/89666583

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