PAREXEL International has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, we supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries.
Designation : Clinical Data Analyst II
Job description :
a. Assume the ability to meet the requirements of a CDA I with a high degree of proficiency
and autonomy
b. Take responsibility for specific tasks on projects, or acts as the main CDA contact on individual projects
c. Train team members on selected tasks
d. Prepare Data Cleaning Specification
e. Review the Data Validation Specification prepared by the Technical Analyst in GTS
f. Develop or provide input to project specific guidelines, e.g. SAE handling.
g. Initiate the running of study specific programs
Desired Profile :
a. Good computer skills including but not limited to the knowledge of Clinical Trial/Data Management Systems, PMED, knowledge of MS-Office products such as Excel, Word
b. Sound awareness of all relevant regulations, including GCP
c. Ability to successfully work in a ('virtual') team environment
d. Client focused approach to work
e. If required, knowledge of medical terminology and awareness of coding dictionaries (e.g. MedDRA & WHODRUG)
Experience : 2 - 4 Year
Educational Qualification : UG - Biology, Microbiology, Zoology, Bio-Chemistry /Bio-Technology, Biomedical Science | PG : Biology, Microbiology, Zoology, Bio-Chemistry/Bio-Technology, Biomedical Science
Location : Hyderabad
APPLY FOR POST
Deadline : 19/01/12
Designation : Clinical Data Analyst II
Job description :
a. Assume the ability to meet the requirements of a CDA I with a high degree of proficiency
and autonomy
b. Take responsibility for specific tasks on projects, or acts as the main CDA contact on individual projects
c. Train team members on selected tasks
d. Prepare Data Cleaning Specification
e. Review the Data Validation Specification prepared by the Technical Analyst in GTS
f. Develop or provide input to project specific guidelines, e.g. SAE handling.
g. Initiate the running of study specific programs
Desired Profile :
a. Good computer skills including but not limited to the knowledge of Clinical Trial/Data Management Systems, PMED, knowledge of MS-Office products such as Excel, Word
b. Sound awareness of all relevant regulations, including GCP
c. Ability to successfully work in a ('virtual') team environment
d. Client focused approach to work
e. If required, knowledge of medical terminology and awareness of coding dictionaries (e.g. MedDRA & WHODRUG)
Experience : 2 - 4 Year
Educational Qualification : UG - Biology, Microbiology, Zoology, Bio-Chemistry /Bio-Technology, Biomedical Science | PG : Biology, Microbiology, Zoology, Bio-Chemistry/Bio-Technology, Biomedical Science
Location : Hyderabad
APPLY FOR POST
Deadline : 19/01/12
