Jobs at BIOCON "A"

Job Description

• To provide medical support to marketing team in strategizing brand plans and sales team.
• Providing scientific and medical input to  Product Management Team for development of visual aid, LBLs, Recent guidelines, Treatment algorithms, Reference folders and patient education literature.
• Conduct medical and orientation programme on Anatomy, Physiology , various related Clinical conditions and Product based knowledge to newly inducted sales employees.
• To develop Protocol, CRF's and other trial related documents, coordinating with Investigators ethical committee submission for all the Phase IV, PMS and Investigators initiated studies. 
• To meet KOL's and Investigators to develop a mindspace for Biocon and provide scientific support.

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GlaxoSmithKline hiring Biostatistician "A"

GlaxoSmithKline Pharmaceuticals Ltd. (GSK Rx India) is one of the oldest pharmaceuticals company and employs over 5000+ people. Globally, we are a £ 27.4 billion, leading, research-based healthcare and pharmaceutical company. In India, we are one of the market leaders. At GSK, our mission is to improve the quality of life by enabling people to do more, feel better and live longer. This mission drives us to make a real difference to the lives of millions of people with our commitment to effective healthcare solutions.

Post : Biostatistician

Job description 
- participate in the clinical/epidemiological development plan (trial designs, sample sizes, interim analysis, etc.) in collaboration with clinical development managers, safety physicians, clinicians and epidemiologists. In particular, provide statistical, and scientific input into clinical development planning
- be responsible for the statistical designs of clinical/epidemiological studies, creating statistical sections for study synopses and protocols
- input in study set up (case report forms, database, randomization)
- explore new statistical approaches and methodologies through innovative and creative thinking
- propose and evaluate the performance of statistical methods in order to prepare statistical analysis plans
- write and execute SAS programs to analyze the data and to report results creating tables and standard listings
- perform statistical analysis, run simulations and discuss with internal and external experts
- support scientific writers and clinicians to correctly interpret the statistical results and align them with the clinical report conclusions
- write the statistical sections of clinical study reports, statistical publications and prepare materials for publications and create statistical text for clinical study communications
- input in standard processes (review of Standard Operating Procedures, guidelines, definition of new processes needed)

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Sun Pharma: Executive- Global Pharmacovigilance "A"

Job Description

• End to End Case processing in Safety database (Argus)/ application including Case Narrative writing/ medical writing in accordance with source data. 
• Processing of Spontaneous, regulatory, clinical trial and literature cases/ all type of case reports
• Seriousness and Listedness (expectedness/ event labeling) assessment
• Coding of events, drugs, medical history and lab test as per MedDRA & WHO dictionary.
• Reconciliations of records

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Govt Job "A"

The Central Pollution Control Board (CPCB) of India is a statutory organisation under the Ministry of Environment, Forest and Climate Change (MoEF&CC). It was established in 1974 under the Water (Prevention and Control of pollution) Act, 1974. CPCB is also entrusted with the powers and functions under the Air (Prevention and Control of Pollution) Act, 1981. It serves as a field formation and also provides technical services to the Ministry of Environment and Forests under the provisions of the Environment (Protection) Act, 1986.



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Work at BIOCON "A"

Biocon is an integrated biotechnology enterprise focused on the development of biopharmaceuticals. With successful initiatives in drug discovery and development, bioprocessing, manufacturing and global marketing, Biocon delivers products and solutions to partners and customers in over 75 countries. Biocon has the defining science, world class capabilities and a focused vision to deliver the promise of innovative and affordable medicine to a waiting world. Today, Biocon together with group companies employs more than 5000 employees with approxmimately Rs 2500 crore turnover and is expected to grow further during the current financial year .
Job Title : QA Executive FOR Visakhapatnam



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Opening for Clinical Scientific Expert-II at Novartis "A"

Job Description:
Clinical Scientific Expert II is responsible for ensuring the collection, review/ reporting of high quality trial data, and study reporting/publishing in compliance with Novartis processes, GCP/ICH and regulatory requirements. In addition, Responsible for ensuring high quality scientific inputs to the clinical development process and support program level activities as assigned.
• In collaboration with Trial Statistician, support development of Reporting and Analysis Planning (RAP) modules in line with program standards.


• Responsible to provide expert support in development of and implementation of relevant data capture tools in collaboration with CSD, GTL and IIS as documented in data handling plan or equivalent document (e.g. CRFs, protocol deviations, questionnaires, diaries, translations, edit checks) • Responsible for performing expert review of ongoing clinical trial data as outlined in the data handling plan or equivalent, supports GTL to prepare database lock; and performing data reconciliation along the whole trial duration in collaboration with  management.
• Collaborate with Medical Lead/BSL to identify any safety trends; and as needed, reports on trial data to safety and clinical boards (e.g. SMT, GCT, and GPT).

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Hiring Drive : Clinical SAS Programmers in Bangalore 11th NOV 2016 "A"

Job Description:



Locally coordinate and take responsibility for trial level programming activities (analysis datasets, pooled datasets, listings, tables and figures) of individual Phase I-IV clinical trials to support program programmers and statistician in project level activities.
Be responsible for statistical tasks on assigned clinical trials e.g. RAP.
Maintain efficient interfaces with internal and external customers with support of ONC Biometrics management and the Program Programmer/Statistician.
Make certain that documents and specifications are consistent and comply with company standards by providing input into CRF and data structures tables, listings and figures for phase I-IV clinical trials and submission activities.
Program and deliver, according to specifications, analysis datasets, pooled datasets, listings, tables, and figures for phase I-IV clinical trials and for pooled analysis with high quality and within milestones.
In consultation with the statistician, develop specifications for analysis datasets, pooled datasets, and listings
Maintain records for all assigned projects and archiving of trial / project analysis and associated documentation.
Provide input on process improvement initiatives and participate in non-clinical project activities with support from GH

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Medical Coding job at DELL "A"

 Job Description : 

• To work with a variety of medical records and assigns appropriate codes based on medical documentation using CPT-4 and/or ICD-9 and ICD-10 coding guidelines
• Handle a team of 50 medical coders and responsible for their deliverables.
• Develop training materials and update the contents that are relevant to the specialty.

Job Requirement :

• 6+ years of team handling experience along with coding expertise.
• Strong knowledge in human anatomy and physiology along with any speciality of Medical coding
• Active CPC certification is mandatory.
• Excellent communication and presentation skills.
• Leadership skills in working with extended teams.
• Should have very good attitude flexible to work in shifts.
• Understand business requirements and cooperate when needed.
• Any life science graduate (BPT, nursing, medical transcription preferred)

Please send your resume to kathiravan_u@dell.com

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Business Executive_metabolics_cardio-diabetic at BIOCON "A"

Job Description

• To attain or exceed the targeted sales volume in the assigned territory.
• To develop relations with the selected doctors in the assigned territory.
• To implement HO strategies on the field.      

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Medical Coding Jobs "A"

Job Description:

• Design & implement work flow processes.
• Ensure quality of Deliverables
• Interaction with clients and ensure timely communication
• Ensure proper execution of projects
• Monitor the quality of the team
• Accountable for Team performance and Quality
• Conduct and recommend trainings to improve team performance
• Manage Customer Engagement and Client Interaction when needed
• Maintain process documents and ensure regular updates
• Ensure all updates from clients are recorded
• Ensure proper allocation of work to team members
• Participate in conference calls with the clients/ top management
• 
  
• Apply here 

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Freshers Job "A"

Biocon is an integrated biotechnology enterprise focused on the development of biopharmaceuticals. With successful initiatives in drug discovery and development, bioprocessing, manufacturing and global marketing, Biocon delivers products and solutions to partners and customers in over 75 countries. Biocon has the defining science, world class capabilities and a focused vision to deliver the promise of innovative and affordable medicine to a waiting world.
Job Title – Executive
Location – Bangalore/Bengaluru

Experience – 0 – 2 Years



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Project Vacancy – Walk-In Interview @ NIPER "A"

Applications are invited for one position each of Laboratory Technician and Data Entry Operator under AIIMS and NIPER Collaborative project titled “New Biotherapeutic Approaches to the Treatment of Tuberculosis” funded by DoP, MC&F, New Delhi.
Post Name : Laboratory Technician
Educational Qualification : Aggregate 55% marks in M. Sc. biochemistry, biotechnology, zoology, microbiology, life sciences, M. (Pharm) in Biotechnology or Pharmacology.

Upper age limit: 28 yrs. (relaxation: 05 yrs. for SC/ST/PH/OBC/woman candidates). Qualification/experience can be relaxed for deserving candidates with relevant experience in the project area.



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PPD hiring for Clinical SAS programming "A"

Job Description

Coordinates the development and implementation of Standard Operating Procedures and Working Practice Documents. Interacts extensively with a multi-disciplinary senior management team to identify critical needs and develop strategic initiatives.
Coordinates process improvement and implements programming standards.
Provides programming oversight for strategic client relationships, and/or oversight for significant client portfolios.

Understands and follows department's working practice documents and SOPs, and contribute to their development as needed.
Understands and follows appropriate corporate SOPs.
Participates in client contract negotiations when modifications are required.
Participates in senior management meetings and be an active participant in long range department planning.
Interacts with business development and visits client sites in an effort to develop client relationships for current and future projects.
Increases knowledge base and professional skills of staff in areas including programming technology and techniques, clinical trials, and the pharmaceutical industry through on the job training, mentoring, and internal or external training courses.

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Walkins at Cognizant for Pharmacovigilance "A"

Job Description

Walk-In Event for Pharmacovigilance role for Mumbai Location :-

Job Responsibilities :-

• Working knowledge on Med DRA
• Track all adverse event reports received and completed
• Review and assess all source documents, and compile data in an adverse event report
• Data enter report into the client safety database
• Code adverse events in the client safety database
• Release report to client through client safety database

Walk-In Details :-

Work Location :- Mumbai

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Jobs in WHO "A"

WHO began when our Constitution came into force on 7 April 1948 – a date we now celebrate every year as World Health Day. We are now more than 7000 people working in 150 country offices, in 6 regional offices and at our headquarters in Geneva.
Vacancy Notice No: SE/CO/NPO/2016/FT16
Title : National Professional Officer (AMR & Labs)
Grade : NO-C
Contract type : Fixed-term Appointment
Duration of contract : Two years
Date : 14 October 2016
Application Deadline : 4 November 2016 (21 day(s) until closing deadline) Currently accepting applications

Duty Station: New Delhi, India

Please visit the following websites for detailed information on working with WHO:
http://www.who.int – To learn more about WHO’s operations

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BCIL hiring Life Science candidates "A"

Biotech Consortium India Limited (BCIL) is a company promoted by the Department of Biotechnology, Government of India with shareholding from the All India Financial Institutions and corporate sector for facilitating commercialization of biotechnology.BCILhas been providing specialized consultancy in different areas of biotechnology to various Government departments and private organizations. It has successfully undertaken a number of assignments for Government and other agencies such as preparation of feasibility studies/Detailed Project Report for commercial biotech ventures /Market Survey for biotech products/technology. BCIL is looking for suitable candidate having desired profile as mentioned below:
Position level: Project Officer (Consultancy)

Nature of job: Tenurial post on contract for three years (extendable on yearly basis based on performance). Promising candidate would be considered for suitable
permanent position in the company during the tenure.

How to Apply :
Interested candidates fulfilling the desired qualification and experience may apply only through e-mail along with their recent photograph, detailed resume and profile summary strictly in the prescribed format given below to: shuklashivkant@biotech.co.in

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Drug Safety Physician required "A"

Job Description 


Report preparation [e.g. Periodic Safety Update Reports (PSURs), Addendum PSURs, Bridging Reports, PSUR Line Listings, US PADERs] from aggregate data for products, in accordance with client conventions and requirements;
Quality checks of aggregate reports; Signal detection-related analyses and reports including cumulative analyses, issue event analyses, Drug Safety Reports , review of published literature and case listings; Vigilance over important/designated medical events;
Interaction with client personnel to discuss potential signals and issues detected with products; Support preparation and maintenance of Risk Management Plans;
Follow-up and interaction with clients to obtain incomplete/missing information, with a view to resolving and clarifying issues;
Performing medical review of individual case safety reports (ICSRs); performing medical review of narratives for Clinical Study Reports (CSRs);
Providing medical advice to drug safety scientists to assist them with processing of ICSRs and CSR narratives;
Maintaining an excellent knowledge of the adverse event safety profile of assigned drugs, labelling documents, and client guidelines and Standard Operating Procedures (SOPs);
Maintaining an awareness of global regulatory reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for report submissions;
Maintaining records in compliance with guidelines and SOPs

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Recruitment drive at Novartis, Bangalore "A"

Job Description

Novartis Healthcare is hiring ...!



Job location : Hyderabad.
Golden opportunity to meet us directly in Bangalore over a weekend - 12 NOV 2016 @ 9:00 AM

Venue: Will be updated here soon.
.

1. Trainee / Junior Programmers - 1 - 3 Yrs..
2. Statistical Programmer -      3- 5 Yrs.

Job Description:
Locally coordinate and take responsibility for trial level programming activities (analysis datasets, pooled datasets, listings, tables and figures) of individual Phase I-IV clinical trials to support program programmers and statistician in project level activities.
Be responsible for statistical tasks on assigned clinical trials e.g. RAP.
Maintain efficient interfaces with internal and external customers with support of ONC Biometrics management and the Program Programmer/Statistician.
Make certain that documents and specifications are consistent and comply with company standards by providing input into CRF and data structures tables, listings and figures for phase I-IV clinical trials and submission activities.
Program and deliver, according to specifications, analysis datasets, pooled datasets, listings, tables, and figures for phase I-IV clinical trials and for pooled analysis with high quality and within milestones.
In consultation with the statistician, develop specifications for analysis datasets, pooled datasets, and listings
Maintain records for all assigned projects and archiving of trial / project analysis and associated documentation.
Provide input on process improvement initiatives and participate in non-clinical project activities with support from GH
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Vee technologies hiring Medical Coders "A"

Job Description

Immediate Openings for IP-DRG Medical Coding -  @ Vee Technologies 
Job Description: 

2+ Years of experience in IP-DRG Coding.

Coding certification like CIC, CPC, CCS, CPC-H, CCS-P. is added advantage.Apply here

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Freshers Jobs @ Syngene "A"

Incorporated in the year 1994, Syngene International is one of India’s premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area. Based in Bangalore, Karnataka, the Company is situated in a 90 acre Special Economic Zone with over 100000 sq. mt of built up facilities.
Job Title – Research Associate/Senior Research Associate
Experience – 0-1 years

Location – Bengaluru/Bangalore



Job Description –
The candidate is expected to perform electrophysiology experiments, prior electrophysiology experience not mandatory, will be trained in-house Will be responsible for data analysis and documentation Should be able to work well with other scientists in the team.

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