Walk in Interview for Tablet Manufacturing on 6th February 2014, Thursday, Timings - 10:00 am - 01:30 pm at Cadila Healthcare Ltd, Sarkhej- Bavla N. H No.8A, Near Modern Denim, Moraiya, Tal Sanand, Dist- Ahmedabad 382 210 |
Opening in Tablet Manufacturing for Technical Supervisor/ Sr. Techinical Supervisor/ Officer |
Candidate Required Profile : |
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inVentiv Health Clinical hiring Sr. Statistical Programmer || Life Science graduate eligible |
Job Description : |
· The Sr. Statistical Programmer is a member of the Biostatistics team and plays a lead role in performing all SAS programming tasks required for clinical trial analysis and reporting. |
· This position works closely with other members of the Biostatistics, and Data Management departments on various clinical projects. |
· May function as Lead Statistical Programmer on multiple projects. |
Project Co-ordinator |
by Cliantha Research Limited in Vadodara/Baroda |
Experience: 0 to 1 yrs. | Opening(s): 2 Posted on: 29 Jan |
Job Description |
1. Handling of BA/BE projects from start to closure |
2. Communicating and co-ordinating with other departments regarding on going projects |
3. Communicating with sponser and IEC |
4. Review of protocols, CRF & ICF. |
5. Conducting protocol training. |
6. Montotring of on-going projects. |
*Sr. Clinical Data Coordinator |
Quintiles - Bangalore |
Posted 2 days ago |
Qualifications : |
• A Bachelors/ Masters degree (preferably in Health Sciences, Science or Clinical) |
• Other relevant degree with minimum 1-2 years of relevant work experience (clinical trials experience in function similar to DM) and a total work experience of at least 4 years. • A background in Medical Terminology, Pharmacology, Anatomy, and Physiology required for many tasks. • A thorough understanding of clinical drug development process. • The position expects excellent organizational, communication, and data management skills. |
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Clinical Trials Assistant |
Quintiles - India |
Posted 7 days ago |
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES |
• Awareness of knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and |
International Conference on Harmonisation (ICH) guidelines |
• Knowledge of applicable protocol requirements as provided in company training |
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint |
• Strong written and verbal communication skills including good command of English language |
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Apply for Medical coder position at Accenture |
Job Description : |
· Graduates in Life Sciences with 1 to 3 years of working knowledge in encoding Serious Adverse Events information according to Medical standards may apply. |
· Experience with MedDRA and WHODD coding standards is a prerequisite. |
· Qualification : Graduates/ Postgraduates in Life Sciences |
· Location : Chennai |
· How to Apply : |
· Interested candidates can apply online using the link below: |
As Team Lead – Safety Repoting & IT you will be part of a young and dynamic team currently consisting of 93 dedicated employees. Close collaboration with our colleagues in Denmark is essential. |
The job entails daily management of the Safety Reporting & IT team, for ensuring employee training, task allocation, optimization of the working processes and, importantly, for daily interaction with the Global Safety organisation in Denmark. |
The tasks demand self dependence and competence in making decisions, as well as flexibility, a good comprehensive view and a many-functioned, often international, co-operation. Conduct 3P, individual development plans, job descriptions and performance evaluation. |
In addition to the management responsibility, further tasks for this exciting and challenging role include, data extraction, using SAS and SQL, from the Oracle based safety database, on going systematic data compilation and initial review of safety information. This is to develop customized summary reports based on internal and external requirements. Further tasks will be within the area of optimized automated report generation using SAS and SQL. |
Also review and verification of SAS and SQL programmes and database data verification and validation. Qualifications |
You have documented experience of 5+ years from current/former positions in the pharmaceutical industry. Experience utilising databases, preferably as SAS/SQL programmer. Prior experience in either project management or people management within drug safety and/or clinical drug development is an advantage. You have an advanced knowledge of database technology (i.e. SQL, Business Objects, TOAD, SAS, and Oracle) and other relevant IT technologies. You use Microsoft Excel on an advanced level. Good ability to guide and instruct other employees on a professional level. |
You are diligent and have an eye for detail. You show a high level of flexibility and you have excellent communication and cooperation skills. Furthermore, you have a good sense of humour. We invest a lot in both professional and personal development and have a thorough individualised development plan for each employee. As part of your job you will receive intensive training in Pharmacovigilance. Contact |
Please send your application marked ”Team Lead–Safety Reporting & IT” to GSGSCHIRING@novonordisk.com. Deadline: 5 Feburary 2014. |
Position: Medical Writer (BPO Company) Exp.: Fresher / Exp. CTC: Up to 1.50 lac p.a. Job Location: Pune (Bibvewadi) Job Profile: Data Entry & Management, Medical Writing Skills: good communication, fluency in English. Interview Venue: Bibwewadi Interview Date & Timing: 3rd Feb 2014 between 10.00 PM to 11.30 PM For details please contact: Mr. Bharat 8983455881 B.Pharm, M.Pharm Experience: 0 to 2 yrs. Posts: 3 |
1. D Pharma /BPharma with 0-1 year of experience. 2. Billing, Picking and dispensing. 3. Should be willing to work in all the shifts. 4. Should have Karnataka registration Experience: 0 to 1 yrs. Posts: 2 Posted on: 30 Jan |
Clinical Data Programmer II |
Icon - Chennai |
Posted 1 day ago |
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, skill, and/or ability required • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions, • USILATAM/CAN, At least 4 years prior experience in clinical data programming. • EU/APAC: Proven experience in clinical data programming. |
QC Specialist, Scientific and Medical Writing |
by Cactus Communications in Mumbai |
Experience: 2 to 5 yrs. | Opening(s): 2Posted on: 31 Jan |
Desired Candidate Profile |
Education: |
UG - Any Graduate - Any Specialization PG - M.Sc - Any Specialization Doctorate - Ph.D - Advertising/Mass Communication |
This position requires: |
· Minimum 2 years of experience in the medical writing industry; freshers with substantial knowledge of the publication landscape and with published papers are also eligible |
· PhD or Masters degree in Research, or equivalent industry experience |
· Ability to work efficiently and independently, multitask, and prioritize |
· Excellent attention to detail, and zero tolerance to errors |
· Ability to concentrate and work under pressure and meet tight deadlines |
· Excellent written and oral communication skills |
· Functional with Microsoft Word, Excel, and PowerPoint |
· Flexible and adaptable to changing project priorities and work assignments |
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Contact Details |
Recruiter Name: Melissa Dias |
Contact Company: Cactus Communications |
Address: Off Link Road Andheri (West) MUMBAI,Maharashtra,India |
Telephone: 67148888 |
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