Tuesday, March 30, 2010

Bangalore, Hyderabad; Clinical Research Associate; B.Pharm, M.Pharm; Parexel

Description:
The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, initiation, monitoring and termination of investigational sites in accordance with ICH GCP guidelines.

Experiance: 2-3 years

send resumes to: kirloskar.das@parexel.com

New Delhi; Trainee Clinical Research Associate/Safety/Monitor; B.Pharm; Tech Observer

Tech Observer is a client-centric global Clinical Research Organization (CRO) providing innovative solutions and analytical support for all clinical research needs. Tech Observer works closely with global Pharmaceutical and Biotechnology companies worldwide.

We are looking for a B. Pharm for multiple openings in Clinical Research – Regional CRA, Clinical Data Manager, Clinical Data Coordinator, Drug Safety Associate based in Delhi NCR area and ideally someone who can start immediately- you will be FULLY TRAINED

send resumes to: resume@tech-observer.com.







resume@tech-observer.com.

Bangalore; Safety pharmacologist; M.Pharm; Yuchra Biologicals

Job Description

M.Pharm (Pharmacology) or M.VSc (Pharmacology & Toxicology) with 1 to 2 years relevant Industrial experience


Should be familiar with animal handling and surgical techniques

Should be familiar with cannulation of blood vessels

Knowledge of handling data acquisition systems like Biopac or ADI is highly desirable



send resumes to:
career@yuchra.com

Delhi/NCR, Kolkata, Lucknow; Research Associate; B.Pharma; Client Of NGT

Desired Candidate Profile
B.Pharma candidates with 0-1 yr experience into research profile ...those who are working as trainees may also be considered

Job Description

Candidate with 0-1 yr experience working in pharmaceutical company in research and development role ... those who are working as medical representatives in leading pharmaceutical companies may also be considered


send resumes to:
resume.co.in@gmail.com

Delhi/NCR; Clinical Research Associate; M.Pharm, B.Pharm; Med Devices

Desired Candidate Profile
A minimum of 2 yrs. experience as a CRA/ Monitor in clinical research with exposure to Medical Device Clinical trial Phase II & III is preferred. Should have good knowledge and practical experience of monitoring and close out activities in C.T.

Job Description
Identify potential investigators in collaboration with the sponsor. Monitoring the progress of C.T. & to ensure satisfactory conduct of trials. Ensure site feasibility, preparation and execution of study. Close out activities.

send resumes to: hr.iclhitech@gmail.com

Mumbai, Barielly ,Jabalpur, Meerut ,Ahmedabad, Guntur; Area Sales Manager; B.Pharm; client of Pharma focus

Experience: 2 - 7 Years
Education:B.Pharm
Location: Mumbai Barielly , Jabalpur Meerut , Ahmedabad Guntur
Job Description
Candidate will be responsible to co-ordinate with field staff. To achieve companies objectives.

contact: Girish Telang, 09422008063

send resumes to: pharmafocus@indiatimes.com

Chennai; Medical Coding Executive ; B.Pharm; Perot Systems BPS India Pvt Ltd

Experience: 0 - 3 Years
Location: Chennai
Desired Candidate Profile

 Graduates in BPT/B Pharm with or without experience

 Flexible to work in shifts

Job Description

 Maintain a working knowledge of CPT and ICD-9 coding principles, governmental regulations, protocols and third party requirements regarding billing and billing documentation

 Assure that all services documented in the patient's chart are coded with appropriate CPT-4 and ICD-9 codes. When services are not documented appropriately, seek to attain proper documentation in a timely manner

 Achieve and maintain a high level of accuracy in professional fee coding while maintaining a high level of productivity. Accuracy will be monitored by periodic reviews by Manager

 Conduct a review of patient hospital charts to insure compliance with coding and documentation guidelines and governmental requirements Provide written reports to Manager with results of these audits

 Maintain a working knowledge of required billing system, the registration process and charge entry

send resumes to: Sheethal_Povada@dell.com