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.

Apply now

Apply Now

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

Apply now

Apply Now

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.



Apply here

Apply Now

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



Apply now

Apply Now

Job as Scientific Officer "A"

On line applications are invited for the Posts of the Scientific Officer (Biology), Class-II, in General State Service under the Director of Forensic Science, Home Department (Advt. 47 /2016-17) between date: 18/10/2016, 13.00 Hrs. to date 03/11/2016, 13.00 Hrs.

Post : Scientific Officer

Apply now

Apply Now

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).

Click and Apply

Apply Now

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

Apply now

Apply Now

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

Apply Now

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.      

Apply now

Apply Now

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 

Apply Now

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.

Apply here

Apply Now

Team Member - Regulators Affairs required "A"

Job Description

Participate in the regulatory activities of full spectrum of formulation development, from clinical trials to marketing to post approval activities.
Ensure the appropriate licensing, marketing and legal compliance of the finished dosages.
Review the documents at each stage of formulations development.
Highlight the regulatory issues that can be there and try to resolve them.
Coordinate with R&D, AR&D, QA, etc. to collect the complete set of documents.
Compile the ANDA document to be submitted to FDA.
Ensure the documents are error free and have minimum deficiencies.
Prepare annual reports and send them to FDA.
Manage change controls and deviation controls.
Keep themselves abreast of international legislation, guidelines and customer practices
Develop and write clear arguments and explanations for new product licenses and license renewals.
Advise PDTs on regulatory requirements.
Respond to the queries of Regulatory authorities and customers on time.
Review the process change proposals and provide guidance on change proposals.

Apply now

Apply Now

Vacancy for Pharmacist "A"

National Rural Health Mission is being implemented in the state constituting State Health Mission District Health Missions, State Health Society and District Health Societies. Kerala State Health and Family Welfare Society, named as “AROGYAKERALAM “ at the State level and District Health and Family Welfare Societies, named as “AROGYAKERALAM (indicate name of district)” ” in all the District Headquarters are registered societies under the Travancore Cochin Literary Scientific



Walk In Interview will be held on 25/10/2016 at National Health Mission, Thrissur 

Apply Now

Walkins at NIPER "A"

National Institute of Pharmaceutical Education and Research (NIPER) is the first national level institute in pharmaceutical sciences with a proclaimed objective of becoming a centre of excellence for advanced studies and research in pharmaceutical sciences. The Government of India has declared NIPER as an 'Institute of National Importance'. It is an autonomous body set up under the aegis of Department of Pharmaceuticals, Ministry of Chemicals and Fertilizers, Government of India. The Institute is conceived to provide leadership in pharmaceutical sciences and related areas not only within the country, but also to the countries in South East Asia, South Asia and Africa. NIPER is a member of Association of Indian Universities and Association of Commonwealth Universities.

The Indian Institute of Chemical Technology, Hyderabad as Mentor Institute is conducting Walk-in-Interview for the following position for NIPER, Hyderabad on a purely temporary basis at 09.00 A M on 21st October 2016 at Committee Room of CSIR- IICT Hyderabad:

Eligible candidates may download the application form from our websites iictindia.org or www.niperhyd.ac.in and appear for Interview along with the duly filled in application form supported by Bio-data and one set of attested photo copies of Certificates of educational qualification, age, experience, caste (in case of SC/ST/OBC candidates), latest passport size photograph and the candidates are required to bring all the original certificates for verification. Registration of candidates will commence from 09.00 A.M to 10.00 A.M. on 21.10.2016

Apply Now

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

Apply now

Apply Now

Inventiv Health hiring Safety Associate "A"

Job Description

• Complete data entry in safety database including writing of adverse event narrative and preliminary assessment of event seriousness and expectedness/ listedness as per Reference Safety Information.
• Generate adverse event queries, liaise with the medical reviewers and clients to agree upon the queries, and send request for additional information to the sites/reporter.
• Engage with the Site Monitors to ensure follow up information is obtained from site effectively.
• Forward safety report documents to designated medical reviewer for review.
• Forward completed safety report documents to clients and other relevant parties.
• Foster constructive and professional working relationships with all project team members, internal and external.
• File documents according to project specific requirements (electronically or in hard copy as applicable).
• Ensure case files are compliant with SOPs.

Apply now

Apply Now

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

Apply Now

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

Apply Now

Career as Medical Coder "A"

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)

Job Profile : 
Activities

• 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.

Interested candidates may please send their current CV with a recent photo and  cover letter indicating their motivation for the position applied for (150 words) and three references by e-mail with subject line Application for the post of “Medical Coder” to cdsa_admin@thsti.res.in.

Apply Now

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

Apply now 

Apply Now