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mpharm,bpharm,Opportunity for Life Sciences Candidates msc,bsc


Source:
TIMESJOBS.COM
Location:
Secunderabad, Telangana
Date:
03-11-2016
Job Code:
56694217
Categories:
  • Biotechnology & Science
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Job Details

Dear Candidate,Greetings for the day!!!It was really nice to see your resume in one of the job portal i.e. (timesjobs.com) and we have an requirement for Clinical Trial Programmer.& drug safety Associate furthermore we feel that your experience is matching to our requirement.I was just wondering if you are available or know of anyone who is looking for new openings at this time. If so, please apply by emailing your resume along with the contact details and we can discuss further about the job opening.Please feel free to share contact details of any of your friends or former colleagues, who are looking for opportunities.Title clinical Trail Programmer Location Hyderabad.Eligibility All fresher s and candidates with 0-2 year experience can applyCLINICAL DATA MANAGEMENT Job Description- Utilize current study documentation including protocol, Case Report Forms (CRFs), Cleaning guidelines etc.- Conduct in-house data review- Generate and close queries or apply self evident corrections to the data according to the relevant guidelines- Identify and report protocol violations- Manual and Patient Profile review, issue queries- Conduct reconciliation of SAEs, send out queries as required and notify relevant Safety Groups of possible issues for their action- Track and integrate queries- Perform clinical coding if appropriate to role within the project team- Ensure all documents coded for submission to central files- Lock site(s) within EDC system - remove user's data modification privileges- Interact with site (via mail) as required- Perform early and final database QC activities- Update all relevant tracking system on an ongoing basisCandidateprofile- Good computer skills including but not limited to the knowledge of Clinical Trial/Data Management Systems Oracle Clinical / Inform , MS-Office products such as Excel, Word.- Demonstrate a sound awareness of all relevant regulations, including GCP- Ability to successfully work in a team environment- If required, knowledge of medical terminology and awareness of coding dictionaries (e.g. MedDRA & WHODRUG)- Solid interpersonal, verbal and written communication skills- Sense of urgency in completing assigned tasks- Effective time management in order to meet daily metrics or team objectives- Shows commitment to and performs consistently high quality work- Educated to minimum of Graduation in LifeSciences or equivalent experience- Fluent in English
Additional Degree: B.Pharm. (Pharmacy) | B.Sc. (Science) | BDS (Dental Surgery)

Experience: 0-2

Requirements

Bio-Statistician | Bio/Pharma Informatics | Clinical Research | Data Management/ Statistics
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