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Icon Clinical Research India Private Limited

ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialise in the strategic development, management and analysis of programs that support Clinical Development - from compound selection to Phase I - IV clinical studies. ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually st... Read More

Address      ICON Clinical Research No.56/4,Sharadha Towers(Unit II), 2nd floor Nandidurg Road Bangalore India
Website      www.iconplc.com
Holding      No Holding Details

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CDMS Programmer I/ii/iii (central Designer) at Ico

ABOUT ICON: ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialise in the strategic development, management and analysis of programs that support Clinical Development from compound selection to Phase I - IV clinical studies. ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart. To learn more about ICON, please go to www.iconplc.com Job title : CDMS Programmer I/II/III (central Designer) Job Location : Chennai JOB FUNCTIONS/RESPONSIBILITIES: Recognize, exemplify and adhere to ICON's values which centers around our commitment to People, Clients and Performance. As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs. Travel (approximately 0%) domestic and/or international *Participates in study specific database set-up within CDIVIS system (i.e. Oraclo RDC, Phase Forward Inform, Medidata Rave, Cerner Discovere, Oracle Clinical and CRF VVorkManager) *Builds clinical study database CRFMatabase screens per CRF/database Specifications provided by Clinical Programming Leads. *Creates/Programs edit checks per a IDVS *Works closely with centralized CDIVIS Testing Group to ensure all programming issues are resolved in a timely manner and study timelines are met *Completes and maintains all study documentation as per ICON procedures *Trouble-shoots and solves study building issues and edit check programming issues_ May participate in study team meetings as an ad hoc study team member. Attends sponsor audits and assists with in-progress audits, as needed. QUALIFICATIONS/EXPERIENCE REQUIRED: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily_ The requirements listed below are representative of the knowledge, sklI, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Successfully manage multiple tasks and timelines. Ability to perform assigned tasks with moderate supervision. Ability to liaise professionally with team members. Team player with strong verbal and written communication skills. Demonstrated ability to learn new technologies, applications and techniques What is on Offer? Come to ICON and be an important part of a well-respected and growing company that believes the details of your career are every bit as critical as the work you do. You will be valued for your passion, commitment, individual perspective and personal contribution to the success of this company. Successful candidates can enjoy all the benefits associated with working for a truly global company including a highly competitive benefits package. We also encourage work/life balance, offer training and development, provide flexible working arrangements etc. Salary:Not Disclosed by Recruiter Industry:Pharma / Biotech / Clinical Research Functional Area:Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology Role Category:R&D Role:Bio-Statistician

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Vacancy type:

Full Time

Contact Mode:

not provided

Fax:

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Contact Name:

HR

Job Duration:

not provided

Phone:

not provided

Email:

ganga.ashok@docsglobal.com

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