Last day to apply for 10 qualified Pharmacopoeial Associates in different projects @INDIAN PHARMACOPOEIA COMMISSION MIN. OF HEALTH & FAMILY WELFARE GOVERNMENT OF INDIA

No. IPC/1016/2007-08 (Vol. II)                                                       Dated: June 06, 2014.

VACANCY CIRCULAR

            The Indian Pharmacopoeia Commission is an Autonomous Body set up under the Ministry of Health & Family Welfare, Govt. of India primarily with the objectives of regularly updating the Indian Pharmacopoeia by publishing new edition and its addenda, National Formulary of India and other related tasks such as preparing, certification and distribution of reference substances. It also acts as national Coordination Centre of Pharmacovigilance Programme of India.

            We are looking forward for 10 qualified Pharmacopoeial Associates in different projects on contract basis having Master’s degree in Analytical and Organic Chemistry. Preference will be given to young, dynamic personnel having 2-3 years experience in drug testing and analysis of Active Pharmaceutical Ingredient (API) and Organic Synthesis, handling of modern analytical instruments alongwith good knowledge of computers @ Rs. 20,000/- per month.

            Applications are invited from citizens of India on the application format which can be downloaded from the website: www.ipc.gov.in of the Commission together with attested copies of supporting documents within 15 days of its publication in the news paper. The competent authority reserves the right to increase or decrease the number of vacancies and reject any/or all applications received without assigning any reason. Selected candidates will be employed through manpower system.

                                                                                                                      (I.J.S. Oberoi)

                                                                                                                 Admn. Officer (I/C)

                                                                                                                                 

Vacancy in Panacea Biotec for the post of Sr. Executive (Clinical Data Management) B3

Post: Sr. Executive (Clinical Data Management)

Job Description

• Responsible for programming of edit checks based on the approved edit specifications document.
  
• Create, implement and execute validation procedures to build and maintain discrepancy database set-up for paper based and/or web based (RDC) clinical data management systems (CDMS) in standard format.
  
• Create and review (electronic) Case Report Forms per Protocol and Annotated Case Report Forms
  
• Write, review and maintain eCRF completion guidelines, data management plan(DMP), Data Validation Plan (DVP, e.g.
  
• Perform or assist in  all aspects of DM process as related to processing QC /review/ UAT and subsequent updation of the findings of the data.
  
• Write and review DM SOPs in accordance with GCO and ICH guidelines, develop associated training and competency testing
  
• Clean data for study close out and perform all database lock procedures
  
• Work in conjuction with Clinical Operations, Clinical Research, and other operations to ensure, accurate, efficient and complete data collection
  
• Contact Metalink and/or Oracle Clinical User Group for validation related issues. As required, based on the response shall suggest IT team about bug fixation / patch updation.
  
• Solve operational problems related with database (front end) and CDM processes.
  
• To perform all related activities of data management like data entry, data coding, data reconciliation and SAE.
  
• To assist manager in holding QA audits and  providing Corrective and Preventive action plan.
  
• Must have experience in CDM with more than 3 years
  
• Well versed with Oracle Clinical/ Remote Data Capture (OC/RDC) specially programming, SQL, PL SQL.
  

Additional Information:
Experience: 3-4  Years
Age: 22-40 years
Location: Delhi
Education: B.Com/B.Sc/B.Pharma etc & Diploma/degrees in Information Technology(IT)/Profesional qualification etc
Industry Type: Pharma/Biotech/Vaccines
Functional Area: CR
Last Date: 19^th July, 2014

Apply/Forward your Resume, corporate@panaceabiotec.com

Experienced M Pharm are required as Research Scientist in Sponsor Company @ Gurgaon, "D3"

Job Title : Research Scientist

Department : Formulation Development

Educational Qualification

M.Pharma in Pharmaceutics from a reputed university

Experience

2-3 years of experience in generic formulation development of injectables for regulated markets(US/EU/Japan) from reputed company

Location

Gurgaon

Description

RESPONSIBILITIES:Planning, coordination and execution of product development activity for global markets.
Evaluation of literature and patents related to products under development.
Planning of stability studies and reviewing of development and stability data.
Compilation of Technology Transfer Dossier related documents.
Scale-up and technology transfer of products to manufacturing locations.

TECHNICAL EXPERIENCE:Handling of Para IV ANDA products for US market.
Good understanding of regulatory requirements of global markets.
Good understanding of Patent and IPR strategies.
Execution of exhibit batches and technology transfers to manufacturing locations.

PERSONAL ATTRIBUTES:Commitment, ownership, integrity, adherence to time lines.
Should have good planning and organizing capabilities.
Should be self motivated and having positive attitude.
Should have good drafting and communication skills.
Should have good team spirit.

About the Company:

Fresenius Kabi is the leader in infusion therapy and clinical nutrition in Europe and in its most important countries of Latin America and Asia Pacific. Within I.V. generic drugs, Fresenius Kabi counts among the leading suppliers in the U.S. market.

All over the world more than 30,000 employees are committed to improving the quality of life of critically and chronically ill patients with innovative products for patients in hospitals and outpatients.

To Apply for this job

Sr. Executive (Clinical Data Management) B.Com/B.Sc/B.Pharma etc & Diploma/degrees in Information Technology(IT)/Profesional qualification etc @ Panaceabiotech, New Delhi -"D1"

Desired Profile  Responsible for programming of edit checks based on the approved edit specifications document.
Create, implement and execute validation procedures to build and maintain discrepancy database set-up for paper based and/or web based (RDC) clinical data management systems (CDMS) in standard format.
Create and review (electronic) Case Report Forms per Protocol and Annotated Case Report Forms
Write, review and maintain eCRF completion guidelines, data management plan(DMP), Data Validation Plan (DVP, e.g.
Perform or assist in  all aspects of DM process as related to processing QC /review/ UAT and subsequent updation of the findings of the data.
Write and review DM SOPs in accordance with GCO and ICH guidelines, develop associated training and competency testing
Clean data for study close out and perform all database lock procedures
Work in conjuction with Clinical Operations, Clinical Research, and other operations to ensure, accurate, efficient and complete data collection
Contact Metalink and/or Oracle Clinical User Group for validation related issues. As required, based on the response shall suggest IT team about bug fixation / patch updation.
Solve operational problems related with database (front end) and CDM processes.
To perform all related activities of data management like data entry, data coding, data reconciliation and SAE.
Solve operational problems related with database (front end) and CDM processes.
To assist manager in holding QA audits and  providing Corrective and Preventive action plan.
Must have experience in CDM with more than 3 years
Well versed with Oracle Clinical/ Remote Data Capture (OC/RDC) specially programming, SQL, PL SQL.
Must have experience in CDM with more than 3 years
Experience  3-4 years
Age  22 - 40Years
Industry Type  Pharmaceutical
Functional Area  Clinical Research
Education  B.Com/B.Sc/B.Pharma etc & Diploma/degrees in Information Technology(IT)/Profesional qualification etc
Email  corporate@panaceabiotec.com, rohitkumar1@panaceabiotec.com
Website  http://www.panaceabiotec.com/
Job Posted  June 19, 2014

Vacancy for B. Pharm/ M Pharm/ BSc Life Sciences Freshers as Clinical Coordinator @ Baxter , D5

Job Title: Clinical Coordinator

Job Description:

·         Provide efficient and high quality training and support to existing dialysis patients by visiting them at home. The Patient follow up by the Clinical Coordinator will include the following:

·         Every patient should have a baseline report filled immediately after catheter insertion

·         Every patient will be visited by a Clinical Coordinator at least once a month on topmost priority.

·         The Clinical Coordinator will diligently fill the patient follow up sheet after probing the patients for their well being. The Clinical Coordinator will examine the patient for their physical signs and symptoms of malnutrition, fluid overload, anaemia, level of activity, depression and record them in the follow up sheet. The Clinical Coordinator will use the HRA chart to assess the risk status of the patient.

·         The Clinical Coordinator will be responsible for monitoring bag sale index and assess the patients for their compliance on the therapy.

·         The Clinical Coordinator will consult the Clinical Team Leader or the Area Clinical Coordinator and the Nephrologist in managing complications.

·         The Clinical Coordinator reports patient coverage and losses in their weekly report every Monday to the Clinical Team Leader and the KAM. Clinical Coordinators are accountable for loss reporting

About the Company:

BaxterInternational Inc., through its subsidiaries, develops, manufactures and markets products that save and sustain the lives of people with hemophilia, immune disorders, infectious diseases, kidney disease, trauma, and other chronic and acute medical conditions. As a global, diversified healthcare company, Baxter applies a unique combination of expertise in medical devices, pharmaceuticals and biotechnology to create products that advance patient care worldwide.

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Hurry for Walkin Hiring Freshers in Insurance transcription for Day shift @ Genpact Pvt Ltd, Noida, 30 vacancies only 3 days left, "D1"

Job Description

Transcribe voice of insurance agent and claimant in the computer using transcription system. Hiring Freshers + Experienced (Same field) Candidate need to be expert in transcription. (For experienced Candidates) Freshers will be given proper training on Transcription before On-boarding. Handling of pedal, tape, earphone and transcription keyboard. Candidate should have experience in Transcription field. (For experienced Candidates) Transcribe the allocated pages and upload them in the system. Education : Complete Graduate ( BA , B.COM , BSC , BA , B.PHARMA, B.tech , etc) JOB LOCATION : NOIDA SHIFTS : DAY Salary -  1,30,000 - 1,60,000 (FRESHERS)  1,60,000 - 2,80,000 ( EXPERIENCED) If interested Walkin at the below mentioned Venue: GENPACT ITES SEZ,Plot No 21 & 22 Unitech Infospace,Tower 8 Upper Ground Floor NOIDA SECTOR - 135 (You can board Genpact Bus by the name of "CITY LIFE" from the Botanical garden Metro Station Parking Area. ) DATE : June 5th - June 21st (Except Sunday) TIMING: 10:00 AM - 2:00 PM Must carry: CV Photograph Original ID Proof Contact : ESHITA 9811530040 For Scheduling Interviews. Write "Eshita Kalia - Transcriptionist"  On top of your CV. Desired Candidate Profile: Excellent typing speed Strong computer skills Basic Knowledge of MS office Toggling between applications on Screen Ability to meet deadlines Ability to handle multiple priorities within strict time constraints Candidate should have experience in Transcription field only. (For experienced candidates) To visit company website.

Manager/ Assistant Manager- Clinical Research Required @ Panacea Biotech - Just 3 Yrs Exp reuired, "D4"

Role: Assistant Manager Clinical Research Education: Medicine/ Pharmacy / Life Sciences Experience: From 3-5  Years in CR industry Salary: As per industry norms Location: Delhi Job Description Desired ProfileTo review and approve clinical trial/ BA - BE studies documents To provide protocol training and execute discussions with CRAs and project manager To provide medical support to the study team during site evaluation, selection, regulatory and EC approvals, study initiation, conduct and closeout To prepare study report, coordinating with PM to obtain investigator’s / opinion/approval and finalization To be a sponsor’s medical monitor for in-house as well as outsourced clinical trials/BA – BE studies To provide literature support for clinical trials, marketed products and for regulatory submissions To do medical writing for regulatory submissions for products: SmPC, Package inserts, Patient information leaflet and Technical reports Active involvement in new product development program and in project review meetings for Panacea Biotec products To prepare and review Standard Operating Procedures To ensure presentation/publication of the results of clinical trials/ BA – BE studies in national/international conferences and journals To coordinate with project manager to provide preventive and corrective action plan of QA audit To assist AGM and senior management in CRO evaluation, selection for outsourcing clinical trial/BA – BE studies To coordinate with partner CROs for Protocol and other Clinical trial document finalization, and providing medical support during Site evaluation, selection, regulatory and EC approvals, study initiation, conduct and closeout for outsourced clinical trials/BA – BE studies. To Apply here

Fresher Candidates who have done SAS or have been trained on SAS (Base Advance or Clinical Research) can apply, Data Management in NCR, "D3"

Position -  Project / Clinical Research Analyst /SAS Analytics

Department -  SAS Analytics Clinical Research

Educational Qualification: B Pharma, Biotech, M Pharma, Health Care Domain, B Tech from a premier institute. MTech / MBA Finance from a reputed institute would be an added advantage

Responsibility

Research Management: Project Management, Report  Execution, QC, Work Process and Quality Management Lead projects that include quantitative/financial analysis like forecasting, modeling and valuation

-        Ensure seamless delivery

-        Knowledge Management: Transfer knowledge to team members.

-        Lead a team of Analysts

-        Making Business Reports on Clinical Data Management

-        Working on Research reports

-        Working on Bioinformatics

-        Using SAS tool to work on clinical data & Meta Data

-        Reporting to the VP for Daily and Weekly predictive reports and working on Forecasting Modules of Clinical Research

Typical Experience: 0-5 years (Fresher’s Can apply - Freshers Trained on SAS)

Skills and Expertise

•        Strong quantitative background with experience

•        Ability to analyze quant/qual information to draw logical

         conclusions

•        Proficiency in MS Excel/ VBA/statistical / packages

•        Good communication and presentation skills

•        Experience in healthcare industry would be an added advantage

•        Familiar with US & Europe Pharma markets: added advantage

Note- Candidates who have done SAS or have been trained on SAS (Base &

Advance or Clinical Research) can apply

Fresher’s are also preferred (Trained on SAS Foundation)

Salary

Fresher’s - 3.20 lakh per annum

0 to 1 year - 3.80 lakh per annum

2 - 4 years - 4.50 lakh per annum

PATH, looks for Program Officer in Delhi region with minimum of 2 years CR experience. Apply today for good salary, "D2"

Role: Program Officer

Education: Medicine/ Pharmacy / Life Sciences

Experience: From 2- 7 Years in CR industry

Salary: As per industry norms

Location: Delhi

Job Description

This role is contingent upon funding.

PATH is an international organization that drives transformative innovation to save lives and improve health, especially among women and children. We accelerate innovation across five platforms—vaccines, drugs, diagnostics, devices, and system and service innovations—that harness our entrepreneurial insight, scientific and public health expertise, and passion for health equity. By mobilizing partners around the world, we take innovation to scale, working alongside countries primarily in Africa and Asia to tackle their greatest health needs. Together, we deliver measurable results that disrupt the cycle of poor health.

The project called Clinical Development Training Program (CDTP) aims to strengthen the clinical research capacity in India. The project will enable trainings and provide resources to meet the ultimate global need for safe, effective, and affordable medicines by establishing advanced resource centers at premier research institutions in India. The program intends to provide sustainable support in major areas of clinical research, viz. pharmacovigilance, advance data management and training, and ethics.

The project called Visceral Leishmaniasis (VL) Program aims to support the national pharmacovigilance system for drugs used for VL in Nepal and Bangladesh, and alsoregistration and preparation for adoption of Paromomycin IM injection by Government of these countries.

PATH is seeking a Program Officer with clinical research and scientific writing experience for Clinical Research, Visceral Leishmaniasis project, and Clinical Development Training Program in New Delhi. As a core member of the project’s operations team, the incumbent will be responsible for supporting all aspects of assigned clinical research projects and the CDTP project under the overall guidance of the Project Team Leader.  Specific responsibilities include:

·    Responsible for writing documents like clinical study protocol, informed consent documents, study and project reports and manuals, and proposal development.

·    Responsible for supporting a moderate to large team or multiple small size protocols with minimal to no supervision.

·    Perform monitoring visits for observational studies, as required. 

·    Build relationships with investigators and site staff.

·    Responsible for the completeness and quality of the on-site files, respond to site issue alerted from sites.

·    Update all relevant tracking systems on an ongoing basis.

·    Provide support for management and execution of PATH’s clinical development training program in consultation with the Team Leader, Clinical Research and Development.

·    Support for executing this project by ensuring stable, strategic partnerships with government agencies, public health partners and academic institutions.

Required Skills

·    Knowledge of clinical study management, and Indian regulatory experience.

·    Proficient in the use of Microsoft Office.

·    Excellent oral and written communication in English.

·    Interpersonal skills and ability to work in a team and with external stakeholders/partners.

·    Ability to travel approximately 25%.

·    Exceptional interpersonal and relationship-building competencies coupled with excellent medical writing skills.

Required Experience

MBBS with five years’ experience or MD with three years of experience with experience in functions like clinical operations or medical writing either at a pharmaceutical company or clinical research organization. Understanding of Pharmacovigilance as a subject will be an added advantage. The ideal candidate for this role will have demonstrable experience in the area of clinical research. 

Must have legal authorization to work in India.

PATH is dedicated to diversity and is an equal opportunity employer.

Visit Directly to PATH

Experienced CRA required in Delhi @ Panacea Biotech, CR experience up to Years can apply for the job, "D1"

Role: Clinical Research Associate / CRA

Education: Graduation in Any discipline

Salary: As per industry norms

Location: Delhi

Job Responsibilities:

Desired ProfileTo develop Clinical Trial for Vaccines/BA - BE related documents 

To assist project manager in site selection and training site personnel

To assist in required regulatory submissions & approvals for the conduct of the study

To conduct site initiation visits as needed for training site personnel about the protocol and study procedures

Provide feedback to assigned sites and information regarding detected deficiencies and corrective action needed.

Conduct monitoring visits to assure the integrity of clinical data with respect to accuracy, accountability, documentation, and methods or procedures through review of CRFs, source documents, medical records, and regulatory documents.

Conduct site close out visits to ensure accuracy and completeness of trial related documents and closing of the trial at the site. To keep a close association with site personnel for: patient Recruitment and patient follow-up

Preparation and Maintenance of Clinical Trial Master File

Resolving all trial related queries, raised from Clinical data management

Assisting project manager/managers/ sr. manager to respond to all QA/ Audit findings and coordinating with study sites and vendors for corrective action plans

Provide overall management of clinical trials or clinical programs

Ensure the project is completed within budget, schedule and according to contract specifications

Assisting Managers to arrange literatures and references for articles/publications/presentations

To ensure that data is provided to data management for preparation of validation guidelines for a clinical study, data entry and queries resolution

To prepare Standard Operating Procedures

Apply Here

WNS is Hiring Freshers " Research Associate" _ Walkins on Going in Gurgaon- Dont Miss that , "D4"

Brief Job Description:

• Doing Sourcing, Pre Sourcing, Name Identification.
• Lead generation for search assignments for Executive Search client through secondary research(primary sometimes) for Financial Services sector
• Identifies trendsetter ideas by researching industry and related events, publications, and announcements; tracking individual contributors and their accomplishments.
• Active participation & contribution in discussions on project specific areas

Skills/Competencies: 

• Experience in doing name generation and talent mapping projects for executive search industry,
• Working on database tools like- Factiva, OneSource, and other secondary data resources
• Project management ability to constantly maintain the quality levels across all projects, ability to do multi-tasking
• Ability to understand the dynamics of Financial Service Sector
• Client management establish client relationship with continued support and building the account
• Ability to analyze and synthesize the available data and bring out value-added insights to the client
• Ability to ensure that tasks within areas of responsibility are completed in a timely manner
• Excellent communication skills, and Good interpersonal skills
• Works effectively in a group and collaborates with the team effectively.
• Possess strong sense of accountability and responsibility towards work.

Technical Expertise: 

• Good knowledge of conducting online research (Finding information for Internet).
• Advanced level knowledge of MS Office (Word, PPT & Excel).

Service Agreement: 2 years

Walk-ins are going on.... at below mention time and address:

Time : 10:00am-2:00pm

Venue :  6th Floor WNS global services,

            Infinity Tower A DLF cyber city Near Shankar chowk.

            Nearest Metro Sikanderpur.

Contact Person: Richa Khanna (mention on top of your resume)

To Visit Company Website