Recruitment for M.Pharm as Medical Coder at Clinical Development Services Agency | Emoluments Up to Rs. 50,000 pm

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Clinical Development Services Agency (CDSA) mission is to create, develop, nurture world class clinical product development capacity in India.
CDSA invites applications from high performing professionals with a desire to serve public health needs of the country for the below mentioned administrative position.

Post : Medical Coder (Surfactant Study)

Emoluments: up to Rs. 50,000/- per month consolidated) 12 Months

Age Limit: <40 years

Qualifications and Skills :
1. Medical degree / Life sciences equivalent (BDS/BAMS/BHMS/M. Pharma)
2. Accredited residency training program or equivalent clinical experience
3. Fluent in English - verbal and written
4. Computer proficiency (e.g. proficiency Microsoft Office suite) Skill: Effective verbal and written communication skills, effective team player, interpersonal skills, high learnability, very high level of integrity, ability to work amidst demanding timelines.


Minimum of 2 years’ experience of working in Medical Coding/ Terminology at a CRO or Pharmaceutical Company.

Job profile
* Responsible for Medical coding and review of all safety data.
* Responsible for Medical review of all coded terms for right mapping of VT with SOC and LLT, PT, HLGT, HLT.
* Assist data manager in creating, reviewing and processing Data Clarification Forms, quality control and updating clinical databases related to safety for ensuring data validity as per the protocol.
* Assists in review of manual data listing as needed.
* Manage all phases of data management activities from study startup to database close.
* To complete database close / lock / freeze checklists.
* To perform reconciliation of the clinical database against safety data, laboratory data and other third party data as appropriate.
* Review CRF / eCRF data entry conventions.
* Performing day to day clinical data quality control and data processing according to the principles of Good Clinical Practice.
* Preparing interim reports for clinical trial status and participating in data extraction in collaboration with the statistician
* Assists the Medical team in other miscellaneous activities as required.

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