Opening for the post of Research Scientist @ LONZA "B"

Opening for the post of Research Scientist @ LONZA

Description

 Role Summary

To provide technical support for Primary cell isolations, novel assay set up, development and validation for bio-service team in India and lead pre-clinical services for domestic / international clients.

Independently plan, direct and execute laboratory research, critically analyze data and interpret results, maintaining complete and thorough documentation.

Maintain high level of professional expertise through familiarity with current scientific literature and competitor products/services.

Primary Role Responsibilities

1. Assay development - Responsibilities will include providing technical input to new trends of assays, anticipate major trends of assays in demand by CRP service providers to pharma/consumer care clients, developing novel cell-based assays and executing them in high throughput screens using a variety of readout technologies.

2. Isolation of primary cells from various tissues. Experience in developing 3D-models will be an added advantage.

3. Assays with primary normal/ diseased human cells: To develop difficult functional assays with primary human normal/diseased cells. Efficacy and toxicity assays for consumer/personal care clients using primary cells.

4. Routine screening assays: Experience with GPCR, calcium uptake, ATP, cAMP assays for pharma clients. 

5. Safety/Compliance: Work within safety

Quality Responsibility Maintenance of quality systems for the team by ensuring that all team members comply with processes, procedures and instructions for all activities in which the team participates.

Safety Responsibility

• Is knowledgeable and complies with all pertinent safety policies, rules and regulations.

• Ensure that all team members comply with safety rules and regulations.

Job Scope

Study latest literature and analyses patents / inventions related to primary cell isolations, novel assays, work on bench and train technicians for assay development, screening and validation techniques, data analysis, report preparation, communication with the clients and sales / marketing team of Lonza.

Click here to apply

Apply Now

Work as Associate Scientist/Senior Associate Scientist @ Syngene "B"

Work as Associate Scientist/Senior Associate Scientist @ Syngene

Job description

Developing cell based assays- optimization and assay validation on different assay formats

Screening of the compounds- small and large molecules

Ex vivo assays in tissue samples

Biochemical screens

Data analysis and report preparation

Protocol & SOP writing

LNB maintenance with appropriate QC checks

Lab management

Desired Skills and Experience

MSc-Biochemistry, Cell Biology, Microbiology, Immunology; MS; MTech or MPharm

Experience on GPCRs (FLIPR), 2nd messenger assays and Ion Channel (Automated Patch Clamp) assays

Experience in medium to high throughput screening

Technical experience in developing cell based assays with end points of physiological relevance for inflammation, central nervous system, and metabolic disorders

Flow cytometry and immunophenotyping

Antisense technology

Experience with peptides and large molecules

Click here to apply directly

Apply Now

Vacancies for Team Member - Peptide Production @ Mylan "B"

Vacancies for Team Member - Peptide Production @ Mylan

 

For Us, It’s A Mission

At Mylan, we mean it when we say we work every day to provide access to high quality medicines to the world’s 7 billion people. If you are unconventional, relentless and passionate.  If you believe in doing what’s right, not what’s easy. If you are a doer and have a passion for serving others, we want to talk to you.

Make a Difference

At Mylan, each person has the ability to make a difference. From the providers who sell and market our products to the producers who develop and manufacture them and finally to our business partners who support the providers and producers, we all have a mission critical role. Here’s how this role will help:

·         Knowledge of Aminoacids and peptide manufacturing.

·         Hands on experience on Peptide Synthesis.

·         Hands on experience on Peptide Purification by Prep HPLC.

·         Knowledge of Lyophilization / freeze drying.

·         Knowledge of cGMP practices in the pharma industries.

·         Handling of documentation, qualification work would be an added advantage.

Click here to apply directly

Apply Now

Opportunity to work as Scientist @ WHO "B"

Opportunity to work as Scientist @ WHO

OBJECTIVES OF THE PROGRAMME :

The main objective of HIV/STI/HEP Programme is to strengthen national capacity of member states for planning, implementation and monitoring the prevention, treatment and care of HIV, STI and Hepatitis including systems strengthening and UHC within the global agenda of sustainable health and development

Description of duties:

Under the broad guidance of Director, Communicable Diseases (CDS) and the direct supervision of the Regional Adviser, HIV/STI/HEP and as part of the Regional HIV/STI/HEP Team, the incumbent will have the following responsibilities:

1. Provide technical and coordination support to Member States in strengthening health sector interventions for HIV/STI/HEP prevention, care and treatment including policy development and programme implementation;

2. Provide technical, advisory and coordination support to Member States in strengthening health services related to HIV/STI counseling and testing with focus on community based testing and decentralized service delivery, drug resistance monitoring, pharmacovigilance;

3. Provide technical support for capacity building for implementation of science research, documentation and dissemination of results;

4. Coordinate with national governments, non-governmental organizations, other UN agencies, partner organizations and institutions to promote the implementation and use of WHO guidance on effective interventions;

5. Promote networking of WHO collaborating centres and Centres of Excellence in the Region for HIV/STI/HEP;

6. Perform any other duties as assigned by the supervisor.

Click here to apply

Apply Now

Work as a Researcher @ eli India "B"

Work as a Researcher @ eli India

Location: India(Hyderabad )

Experience: Freshers

Shift Time: 10.00 AM to 7.00 PM (Shifts are likely to change in future)

No of Positions: 30

Apply Job

Qualification : M Pharmacy

Key Skills Needed:   

Prior Experience in developing Database for Market Research Company

Sound knowledge in Disease therapy areas, Clinical trials, Pharmacology, Regulatory Subject

Experience in generating Reports for Global Audience from this Database

Sound Industry Knowledge

Desired Skills:   

Sound Understanding of Market Research Environment for Pharma/BioTech Industry

Ability to Multi task ; coordinate with different tasks

Excellent Data Handling skills and Analytical Skills

Disciplined approach and timeline adherence

Sound Knowledge of Excel

Quality Focus ; Diligent entry of correct records into System

Flexible to working in multiple shifts in line with company requirement

Job Description:    

Ability to gather, analyze and evaluate facts and to incorporate them in set formats

Good understanding of market fundamentals, secondary research techniques

Should be capable to handle multiple tasks end to end simultaneously based on business needs

Meet and Exceed assigned Targets for Database Entries and Report Generation

Overall Responsibility for Deliverables in line with task assigned and within assigned timelines

Sound Understanding of Industry Database System and Development Regimen

Good Data Analytics Know how

Ability to work across multiple data tables in Excel

Click here to apply

Apply Now

Work as Executive - Business Finance @ SUN PHARMA "B"

Work as Executive - Business Finance @ SUN PHARMA

Job Description

Assist in consolidation of monthly and quarterly financial and operational reports, dashboards, and analysis.

Prepare synergy accruals and compute the actual cost savings arising from various cost saving initiatives globaly.

Assist with annual budget and monthly MIS preparation.

Proactively identify opportunities and make recommendations to resolve issues and improve current policies and procedures.

Ad hoc reports and special projects as needed.

Click here to apply

Apply Now

Work as Research Assistant @ INTAS "B"

Work as Research Assistant @ INTAS

Job Description

- Conduct BA - BE / Phase - I Studies (Clinical Part).

- Communication with sponsor & other department with respect to Clinical Phase of studies.

- Subject follow-up coordination.

- Resolve & respond to QC, QA, Sponsor & regulatory queries / audit queries.

Click here to apply

Apply Now

Keys to Success with Clinical Trials "A"

Keys to Success with Clinical Trials

Since clinical trials provide access to novel therapies years before they become available on the open market, some physicians may be curious about participating in the clinical trial process. Indeed, becoming a clinical trial investigator can positively impact a private practice in several ways. First, investigational therapies can provide treatment alternatives for difficult or burdensome cases, such as patients with irritable bowel syndrome, refractory inflammatory bowel disease (IBD), and intractable constipation. Participation in clinical trials can also enhance the practice's standing as a cutting edge practice and can increase the practice's revenue stream without the hassle of insurance carriers. Finally, involvement in clinical trials can renew physicians' academic interchange with peers by encouraging participation in meetings, publications, and lecture series.

Preparing to Make the Commitment

Before becoming involved as a clinical trial investigator, physicians need to consider whether they are ready to make this commitment. Clinical trials require the investment of the doctor's time, the practice's personnel, and other resources, so physicians should evaluate their capacity to meet these needs.

Time

Explaining a clinical trial to patients is a task best performed by the principal investigator (PI), and physicians should consider each patient as a potential study candidate. If extra time cannot be allocated for this discussion, then physicians should not consider enrolling as a clinical trial investigator. Since the patient's trust is with the doctor, the physician must be an active player when enrolling patients; support staff cannot be expected to do all the introductory work. All the physicians in a practice should agree to this undertaking.

Once a trial has started, the physician will need to meet with clinical research organization (CRO) monitors, review protocols, sign off on laboratory work, and be available to staff and patients to answer questions or address misunderstandings of protocol requirements. Also, the PI should plan to travel as needed. The PI will be asked to attend investigational meetings and follow-up sessions, and these requirements will detract from the physician's office schedule.

Personnel

In addition to the doctor's time commitment, involvement in a clinical trial also places burdens on office personnel. One way to meet this demand is to hire a dedicated research coordinator. Physicians should not assume that the practice's current staff will willingly accept added responsibilities; indeed, staff often resent the extra work clinical trials entail, and this resentment may lessen recruitment and sustained enrollment. Failure to sustain enrollment is a major concern, since unsuccessful recruitment will damage the practice's reputation for future trials.

Having a dedicated clinical trial coordinator means that the practice will have the personnel needed to review potential protocols and analyze the practice's database to ensure that the appropriate patient population is being considered for the study. Since quick turnaround is expected in the research industry, clinical trial sponsors may be displeased if a practice takes too long to complete the required regulatory paperwork; the clinical trial coordinator can focus on addressing this need for prompt turnarounds. If a practice can negotiate a contract with indemnification language and governing laws, negotiate a budget, and complete the US Food and Drug Administration (FDA) forms and sponsor-specific forms within 5–7 business days, the practice's involvement in future projects will be much more attractive.

When working with clinical trial sponsors, physicians should keep in mind the perspective of the pharmaceutical company, in which the clock starts as soon as the bench work for discovering a new compound is complete. There are a limited number of years during which the company can capitalize on a new drug before the patent expires and generic competitors enter the market, so pharmaceutical companies have time-sensitive goals for site initiation, enrollment of the first patient, completion of enrollment, attainment of primary and secondary endpoints, and data analysis.

Oversight

Finally, practices that participate in clinical trials should be prepared for constant CRO monitor visits, queries, and reviews of accumulated data. By participating in a clinical trial, the practice is opening itself to added scrutiny, as a number of procedures and guidelines must be reviewed; these include good clinical practice (GCP) guidelines, informed consent policies, adverse event reporting guidelines, and instructions for avoiding coercion in certain populations. An experienced clinical research coordinator can ensure that the practice adheres to standards that meet the GCP definition accepted by the FDA and device and pharmaceutical companies.

Because fulfilling all these tasks in-house will involve a great deal of work, physicians may want to consider partnering with a site management organization or a clinical trial management organization. These organizations can assume many burdensome administrative tasks, although they usually do so in exchange for a hefty share of the budget. These organizations are quite knowledgeable and may negotiate better contracts and budgets, as well as lessen the investment needed in terms of site space and staff involvement, and guide the novice physician or practice through the clinical trial.

Go to:

Principal Investigator: Education and Responsibilities

As the PI, the physician is responsible for numerous aspects of a clinical trial. The PI's first responsibilities are to ensure that the protocol's inclusion and exclusion criteria are met and to consider whether the benefits of participation in the trial outweigh the potential medical risks. In addition, the PI must monitor participants' compliance with study requirements; this can be done via Interactive Voice Response Systems, medical records, drug accountability, and/or follow-up visits. Failure to monitor patients adequately can sabotage the entire study and damage the site's reputation. The choice of appropriate patients for study enrollment is critical to this process.The PI and his or her team must also ensure adherence to the protocol, fulfillment of regulatory responsibilities, and maintenance of data quality. Finally, the PI must update trial enrollees of any new risks or benefits that evolve as the trial progresses.

___________________________________________________________________________

Adv: 

Apply Now

Walk in Drive for Clinical Graduates / Freshers ( Medical Coding) "A"

 Walk in Drive for Clinical Graduates / Freshers ( Medical Coding)

Navigant BPM (India) Private Limited

0 - 0 yrs

Trivandrum

Job Description

The medical coder will abstract the information from the patient medical records, read and interpret the medical documentation and translate the diseases and procedure information in the form of numerical and alphanumerical codes appropriately and accurately.


 They then assign the appropriate codes which correspond to a charge and are eventually converted into dollars which are utilized by insurance providers for compensating the health care providers.

• First 06 months there will be training
• After successful completion of training they will be placed on projects
• Should be flexible in shift timing
      Date: 30-Mar-2016 To 01-Apr-2016
      Time: 10.00 AM To 1.00 PM
      Venue: Navigant Consulting,

Pamba Building,

Techno park.

Trivandrum 695 581.

Contact: 8891136366

Company Profile:

Navigant BPM (India) Private Limited

Navigant Consulting® Services, Headquartered in Chicago with offices in nearly 50 cities throughout North America, Europe, Middle East and Asia,

Navigant has serviced clients in more than 70 countries around the world.Navigant Offers a wide range of financial management services,investigation services, litigation support services, and business management consulting services.

Navigant has acquired RevenueMed India Private Limited, as an ITeS Organization, headquartered in Atlanta, involved in providing revenue cycle services to health-care providers (www.RevenueMed.com).

RevenueMed started its operations in 2002 and since inception, is one of the fastest players in the US health-care market.We operate from 3 facilities at Technopark-Trivandrum, Kerala, and an office in Nagercoil, Tamilnadu, with staff strength of over 1500.  

Apply now

___________________________________________________

Adv: 

Apply Now

Opening for the post of Medical Representative @ Claris Otsuka Private Ltd. "B"

Opening for the post of Medical Representative @ Claris Otsuka Private Ltd.

Job Description

Call Management: High quality detailing / Call Compliance

Product promotion and marketing

Developing & maintaining good relationship with doctors, pharmacist & other hospital authorities

Daily Report submission

Conducting Analysis & participating in Review

Click here to apply

Apply Now