Drug Safety Physician / Medical Reviewer Synowledge PV Services India Pvt Ltd

JOB TITLE: Drug Safety Physician/ Senior Drug Safety Physician

LOCATION: Mysore, India

YEARS OF EXPERIENCE: 0-5 years experience in PV

EDUCATION: MBBS/ MD (Any)

ESSENTIAL DUTIES AND RESPONSIBILITIES: 

As a Medical Reviewer

Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports
Determine regulatory reportability of cases obtained from clinical trials, spontaneous and solicited reports within assigned therapeutic team and across all products/sites, as necessary, and in a timely fashion
Determine seriousness and relatedness across products as assigned
Review and verify appropriate selection of adverse events from source documents, assign appropriate MedDRA code, assess labeling, review narrative.
Acquire and maintain current knowledge of product portfolio and safety profiles for products across therapeutic areas
Escalate complex case issues on client product(s) to the medical review team of the client as appropriate
Identify and resolve case issues, coordinate with client therapeutic teams/site for specific products or functional groups
Communicate and interact effectively within and across all client therapeutic teams, and within functional team management as appropriate
Acquire and maintain knowledge of applicable Global Health Authority regulations
Perform any other drug safety related activities as assigned
Participate in internal and external audits and inspections by clients and health authorities


SPECIALIZED KNOWLEDGE AND SKILLS:

Experience with relevant safety databases and related software applications
Proven experience in customer handling and relationship.
Proven ability to perform task management.
Must have good presentation skills and the ability to give presentations.
Knowledge of the Life Sciences Industry and life cycle of drug.
Relevant product and industry knowledge.
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Opening for Medical Writing for M.pharm/pharm.d Freshers,experienced

 Hiring for freshers -M. Pharm/ Pharm. D at Indegene Lifesystems for Scientific Writing/ Medical Writing.


Kindly find the job description.
Develop content for various deliverables meeting quality requirements as per client satisfaction metrics, with active guidance from the manager

Responsible to develop content as per the timelines assigned

Responsible to follow the best practices in the department regarding - processes, communication (internal & external), project management, documentation and technical requirements like - language, grammar, stylization, content search, summarizing, data conflicts and referencing

Participate in assigned training programs and work on assignments as per requirement

Participate in cent calls as per project requirements

Compliance to quality, confidentiality and security:

Adhere and follow quality systems, processes and policies

Comply to training and specifications


Education : M.Pharm/ Pharm. D - Freshers

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Pharmacovigilance Medical & Scientific Writer With Crest - Pune

• Identifying and evaluating individual case safety reports (ICSRs) of adverse drug reactions from the published literature
• creating summary content in a range of formats (narrative summaries, structured database inputs, electronic formats for regulatory filing ) to support the drug safety reporting and information requirements of pharma industry clients
• Required background and experience: you will have working experience in the pharmacovigilance/drug safety field and a background in medicine or pharmacy
• Ideal experience would include:
• 
  
• Scanning the literature or other data sources to identify reportable adverse drug reactions based on accepted industry and regulatory guidelines
• Detailed evaluation of individual case reports e.g. determining seriousness of adverse events, determination of drug causality, subsuming signs and symptoms into clinical diagnoses etc.
• Familiarity with the reporting and regulatory requirements for pharmaceutical companies as mandated by drug safety authorities

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Process Trainer (pharmacovigilance)-Cognizant Mumbai

• Deliver training on the floor - effectiveness measured through Trainer Feedback Score (from Trainees)
• Ensure associates are assigned to process training refreshers based on QA data on associates performance
• Facilitate Process Training Refresher modules effectively measured through Trainer Feedback Score
• Ensure completion of all compliance courses for all associates tagged to the project within timelines
• Willingness to work in rotational shifts
  Only BPharm/MPharm/BDS/BAMS/BHMS candidates need to apply 

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Drug Discovery Technologies Market 2012-18

Drug discovery technologies play a significant role in the field of pharmaceuticals as they heavily contribute to the introduction of drugs to the market. The application of drug discovery technologies have a significant opportunity in  the launch of drugs for severe diseases such as cancer, cardiovascular diseases, Parkinson’s disease, central nervous system disorders and others. However, the slow growth in the introduction of blockbuster drugs could pose a major threat for the growth of this market.

The major technologies in the drug discovery market are proteomics, genomics, QPCR, DNA and protein microarrays, high-throughput screening, mass spectrometry, laboratory information management systems, microfluidics, gel electrophoresis, chromatography, and protein and nucleic acid isolation.

As the global population ages, there is a growing pressure to keep the healthcare costs under control. Senior citizens are more prone to chronic diseases. It is in the nation’s best interests to keep its population healthy. In addition to this the pressure is paired with the government’s and administration’s responsibility to pay for healthcare. This situation will magnify in intensity if nothing is done to improve the status of treatment and prevention of diseases among the aging population. 

Apart from facing these pressures, the pharmaceutical manufacturers also face an impending surge of expiring patents. This will result in reduced profits of pharma companies. The market players in this field have begun to respond to these factors by restructuring their strategies and bringing innovation in their products thus, improving their productivity and efficiency. Despite these measures, pharmaceutical companies face the fact that drug discovery and development consumes a huge amount of time and money. For instance, drug discovery and development from scratch may take around 15 years and costs about USD 500 million until it is introduced in the market.

Big Data Analytics: The Next Evolution In Drug Development

The drug development process is complex and financially risky. A recent study by The Tufts Center for the Study of Drug Development estimates the cost of developing a new drug at $2.6 billion and suggests that costs of drug development are rising with a compound annual growth rate of 8.5 percent. These rising costs are largely driven by increases in out-of-pocket costs, such as larger clinical trial sizes and higher failure rates for drugs required to demonstrate superiority. Even when considering the efficacy of the 10 highest-grossing approved drugs in the United States, the fact is that for every patient a drug does help, between three and 24 patients fail to show improvement after treatment. Clinicians are typically forced to address this variability in patient outcomes with a trial-and-error approach to intervention, increasing healthcare costs and adding a burden to the patient.

Drug Developers, Providers, And Patients Need A Better Option 

High-throughput technologies are ushering in the era of Big Data in drug development, allowing researchers to assay patients in terms of their genome, epigenome, proteome, metabolome, and microbiome. Precision medicine initiatives are being undertaken to tailor disease treatment by taking into account individual variability in molecular and cellular systems. A biomarker- and technology-driven approach to developing targeted therapies and patient selection strategies has the potential to increase success in the drug development process, decrease cost, and ultimately improve patient outcomes with directed intervention. Read More

S. Pandarinath, Pharmacist, Certified Pharmacovigilance Professional.

Serious Event or Serious Suspected Adverse Reaction in Pharmacovigilance Practice

An adverse event or suspected adverse reaction is considered "serious" if, in the view of either the investigator or sponsor, it results in any of the following outcomes :

-Death
-A life-threatening adverse event
-Inpatient hospitalization, or prolonged of existing hospitalization
-A persistent disability to conduct normal functions
-A congenital anomaly/birth defect

Important medical events that may not result in death, be life threatening, or require hospitalization may be considered serious, when based upon appropriate medical judgment, they may jeopardize the patient or subject and may require medical or surgical intervention to prevent one of the outcomes listed in this definition.

Author- Sirisha Boidapu, Pharmacist, PV Professional

Researchers are studying fish which can repair their own hearts.

Hundreds of thousands of people in the UK are living with debilitating heart failure. They can’t regenerate their damaged hearts. But zebrafish can. If part of their heart is damaged they can repair it in a matter of weeks, just like we are able to mend a broken bone.  That’s why our Mending Broken Hearts Appeal is funding researchers to find out what their secret is.

Because zebrafish are transparent early in their life cycle, it’s easy for researchers to see their hearts and blood vessels grow. Their hearts begin to develop after just 12 hours, and they reach adult size – about 3cm long – in about three months, so they can provide quick research results. Read More

Biological similarity of humans and other animals

Although humans and animals (technically “non-human animals”) may look different, at a physiological and anatomical level they are remarkably similar. Animals, from mice to monkeys, have the same organs (heart, lungs, brain etc.) and organ systems (respiratory, cardiovascular, nervous systems etc.) which perform the same functions in pretty much the same way. The similarity means that nearly 90% of the veterinary medicines that are used to treat animals are the same as, or very similar to, those developed to treat human patients. There are minor differences, but these are far outweighed by the similarities. The differences can give important clues about diseases and how they might be treated – for instance, if we knew why the mouse with muscular dystrophy suffers less muscle wasting than human patients, this might lead to a treatment for this debilitating and fatal disorder. Read More

More investment to characterize animal models can boost the ability of preclinical work to predict drug effects in humans

Mice take the blame for one of the most uncomfortable truths in translational research. Even after animal studies suggest that a treatment will be safe and effective, more than 80% of potential therapeutics fail when tested in people. Animal models of disease are frequently condemned as poor predictors of whether an experimental drug can become an effective treatment. Often, though, the real reason is that the preclinical experiments were not rigorously designed. 

The series of clinical trials for a potential therapy can cost hundreds of millions of dollars. The human costs are even greater: patients with progressive terminal illnesses may have just one shot at an unproven but promising treatment. Clinical trials typically require patients to commit to year or more of treatment, during which they are precluded from pursuing other experimental options. Launching a clinical trial without the backing of robust animal data keeps patients out of tests for therapies that may have a better chance of success.Read More

Frequency of adverse drug reactions

Frequency of adverse drug reactions

Whenever possible, an estimate of frequency should be provided, expressed in standard category of frequency. It is always difficult to estimate incidence on the basis of spontaneous reports, owing to the uncertainty inherent in estimating the denominator and degree of under-reporting. However, whenever possible, an estimate of frequency should be provided and in a standard form.
The following standard categories of frequency are recommended:

Very common
> 1/10 (> 10%)
Common (frequent)
> 1/100 and < 1/10 (> 1% and < 10%)
Uncommon (infrequent)
> 1/1,000 and < 1/100 (> 0.1% and < 1 %)
Rare
> 1/10,000 and < 1,000 (> 0.01% and < 0.1%)
Very rare
< 1/10,000 (< 0.01%)

Current status of clinical research in India

 

Clinical research has grown exponentially over the past decade in India because of cost advantage, treatment naïve patient, qualified doctors conversant in English etc. India was the second most preferred country to conduct clinical trials outside the US in 2009. However, recent years have witnessed a decline in number of trials in India (529 in 2010; 253 in 2012). The number of drugs entering the Indian markets had been gradually reducing even before the current slump in clinical research activity (270 in 2008;140 in 2011; 44 in 2012 and 25 in 2013). This necessitates a relook on the strategy so as to optimise clinical research in Indian context. The problems and possibilities around the clinical research arena can be broadly grouped as capacity building issues and ethico – regulatory ones.

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Regulators and patients driving demand for Phase IV studies, says Quintiles

Full spectrum CROs are well-positioned to service the growing demand for late-stage observational trials driven by regulatory and patient pressure, says Quintiles.

Read More

Omega (Ω)

A measure of disproportionate reporting for drug-drug-ADR triplets in ICSR databases, designed to highlight potential signals of drug-drug interactions. Just like the more established disproportionality measures for drug-ADR pairs, Ω is based on a contrast between the observed and expected number of reports. A positive Ω indicates higher reporting than expected.

Rechallenge

The point at which a drug is again given to a patient after its previous withdrawal.

Dechallenge

The withdrawal of a drug from a patient; the point at which the continuity, reduction or disappearance of adverse effects may be observed.

Salary in Pharmacovigilance for freshers in INDIA

Discover the benefits of collaborating with your central lab partner early in protocol development

Until recently, sponsors and CROs engaged their central laboratory simply for routine safety testing. However, as clinical trial protocols have grown in complexity expert consultation in diagnostic testing at the beginning of protocol development is fast becoming critical to optimize test selection and match clinical diagnostic endpoints to outcomes. 

This e-book explores how collaborating with your central lab partner early in protocol development can help optimize clinical trials, drive efficiencies, avoid potential protocol amendments, and minimize costly study delays.

Read More

Author: Susmitha Pandarinath, Pharmacist, Certified Pharmacovigilance Professional.

Regulators and patients driving demand for Phase IV studies, says Quintiles

Full spectrum CROs are well-positioned to service the growing demand for late-stage observational trials driven by regulatory and patient pressure, says Quintiles.

Read More

Author: Susmitha Pandarinath, Pharmacist, Certified Pharmacovigilance Professional.

What do you mean by pharmacovigilence in drug development process ?

 It is the mission of pharmaceutical research companies to take the path from understanding a disease to bringing a safe and effective new treatment to patients. the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug related problem.

Pharmacovigilance is defined as the detection, assessment and prevention of adverse drug reactions in humans.


It is the process of:

• Monitoring medicines as used in everyday practice to identify previously unrecognised adverse effects or changes in the patterns of their adverse effects
• Assessing the risks and benefits of medicines in order to determine what action, if any, is necessary to improve their safe use
• Providing information to users to optimise safe and effective use of medicines
• Monitoring the impact of any action taken

Scientists work to piece together the basic causes of disease at the level of genes, proteins and cells. Out of this understanding emerge “targets,” which potential new drugs might be able to affect Researchers work to validate these targets, discover the right molecule (potential drug) to interact with the target chosen, test the new compound in the lab and clinic for safety and efficacy and gain approval and get the new drug into the hands of doctors and patients. This whole process takes an average of 10-15 years.

Author: Susmitha Pandarinath, Pharmacist, Certified Pharmacovigilance Professional.

Pharmacovigilance in Drug Development

 Pharmacovigilance (PV) is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug related problem. It collects, records, codes adverse drug reactions analyses and assesses the reports, promotes the safe use of drugs, creates appropriate structures and means of communication needed to perform its tasks.The aims of PV are to improve patient care and safety, improve public health and safety, contribute to the assessment of benefit, harm, effectiveness and risk of medicines, promote education and clinical training, promote effective communication to public and promote rational and safe use of medicines.

The process of drug discovery and development is a long-term, competitive, expensive and complicated process. Bringing the drugs from the bench to the market, that is, from screening and identification of the drug as a compound to its introduction to the market, takes several years of efforts. The complete process of presenting a drug to the patients involves four stages-

1. Drug discovery
2. Drug development
3. Regulatory review and approval
4. Marketing

Pharmacovigilance is the pharmacological science which deals with drug safety including accumulation, detection, assessment, monitoring, and prevention of adverse effects of the drugs.
It is a process focusing on detection of unidentified safety issues, identification of risk factors, quantifying risks and preventing patients from being adversely affected unnecessarily.

Pharmacovigilance plays a critical role at various stages of drug discovery and development process
for example, in clinical research, pharmacovigilance requires submission of the reports on adverse events during clinical trials to regulatory authorities within a specified time frame, notification of such events to all investigators and ethics committees, and a safety review by independent Drug Safety Monitoring Boards (DSMB). Annual reports, a summary and analysis of all the serious adverse events, new safety findings from animal studies, and evaluations of benefit and risk are also required.

Pharmacovigilance also plays a significant role when the drug is commercialized. Reporting the safety reviews is mandatory for companies in a marketing phase. These safety reviews include
-Risk Management Plan (RMP)
-Periodic Benefit Risk Evaluation Report (PBRER)
-The Development Safety Update Report (DSUR)
-Periodic Safety Updates Report (PSUR)
-Phase 4 studies (post-marketing surveillance)

Pharmacovigilance plays a very critical role in drug discovery and development process. It will require comprehensive documentation and severe monitoring at every phase of drug development including pharmacovigilance inspection and audit, risk management, and reporting of ADR medicinal drugs, periodic safety update report, and post-authorization safety studies, additional monitoring, and safety communication.

Author- Sirisha Boidapu, Pharmacist, PV Professional

Drug Discovery-What is all about?

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

• Phase I: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
  
• Phase II: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
  
• Phase III: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
  
• Phase IV: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.
  

Freelance Editors- Pharmaceutical Sciences Cactus Communications

Job Description

 

Cactus Communications is a pioneer in language services, serving more than 60,000 clients across 116 countries. We employ a global team of highly skilled editors who are experts in various academic fields. Were currently looking for specialist freelance copyeditors and substantive editors from all across the world.

Why this is a great opportunity

• Flexibility to determine your schedule and work hours 
• Potential to earn above INR 60,000 per month (based on regular availability) 
• Additional fees of up to 20% 
• No need to relocate. As this is a freelance opportunity, applicants are free to work from home.

What you will do?

Edit manuscripts such that the final text is in standard scientific English and is free of unclear or unidiomatic sentences
Adhere to job-specific instructions and format manuscripts according to the target journal when required
Ensure that all subject-specific conventions are followed

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10 Proven Ways to Reduce the Cost of Clinical Trials

Trimming your study budget is a good thing, right? When you can cut costs without compromising data integrity or accuracy, that's usually a positive. But when cost cutting is only about saving money no matter what, it can increase frustration, impair quality, damage reputations and end up increasing project costs in the long run. There are, however, a number of evidence-based strategies you can use to streamline your research and trim budgets that maintain – and, in many cases, enhance – data quality, staff productivity and employee satisfaction. Read to learn more. Read More

Associate Analyst - Pharmacovigilance (data Migration)

Associate Analyst - Pharmacovigilance (data Migration)

0 - 2 YearsHyderabad / Secunderabad INR 1,75,000 - 3,50,000 P.AOpenings: 100

Walkin Interview from 22nd September to 24th September from 12 PM

Job Description

 Review of source documents in the individual case safety reports for assigned cases in the project Case book-in
Completion of the heads down data entry from source docs to safety data base
Evaluates consistency, completeness, accuracy of safety database, tracking database and source document
Capturing the correct data in the tracking tool, to assist generation of project related metrics
Document case related observations in the tracking tool and communicate the observations to other associate analysts
Be responsible in meeting timelines, and quality standards.
Be responsible for ensuring 100% training compliance to the client assigned training curriculum
Ensure process steps adherence for the assigned project
Ensure adherence to QC/QA plans as applicable
Mentoring new-hires as designated by the senior manager
Any other responsibility delegated by the reporting manager

Eligibility criteria:


The candidates should have a graduate/ Postgraduate Degree in stream with 0-1 year of experience in data entry.
The candidate should have demonstrable proficiency in Microsoft office applications such as Microsoft word, excel and outlook
Ability to work with the team and in  pressure situations
Good English comprehension skills and writing skills .

Walk-in between 12Pm to 3PM from 22nd to 24th September

Education:UG -B.Pharma - Pharmacy
PG - M.Pharma - Pharmacy

Contact Details

Recruiter Name:Kaavya

Contact Company:Tech Mahindra Ltd

Telephone:91-40-0000000000000

Address :Unit No.12, Plot No. 35 & 36, Hi-Tech City Layout ,Survey No. 64, Madhapur ,Hyderabad - 500081 (Telangana),Hyderabad,Andhra Pradesh,India

Website:https://www.techmahindra.com

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Study authors urge IRBs to reject trials that deny babies pain relief

Researchers are urging review boards to reject neonatal clinical trials if protocols require that babies in control groups are denied analgesia.

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Clinical Research Associate Manipal Acunova Ltd.

Job Description

 

Carrying out the tasks assigned by senior executive/ Manager in the required manner. Recording the relevant details in the appropriate workbooks.
Preparing detailed reports immediately at the end of the task relating to the project or as required by your supervisors.
Recruit patients & obtain their consent for trials.
Update Case Record Forms (CRFs) daily & manage external audits

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How Sponsors and CROs Benefit From EDC Efficiencies

Intense competition in the prescription drug market is driving pharmaceutical companies to expedite their drug discovery and development processes. Pharmaceutical companies understand the value of being the first to bring a new drug to market, and it is this knowledge that is leading them to continually seek ways to streamline their clinical trial process.

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Polymers make you go faster, greener, say BASF and Colorcon

BASF, one of the world’s largest chemical companies, has chosen Colorcon to distribute its Kollicoat Immediate Release (IR) tablet coatings.

Read More

Senior Medical Writer: Clinical Evaluation Report (cers) Cactus Communications

Job Description

 

Send me Jobs like this

CACTUS Medical offers medical writing services to multinational biopharmaceutical and devices companies, clinicalresearch organizations, and researchers worldwide. We work with clinicians and researchers to help them communicate their science to the world. We are currently looking to add to our team, experienced medical writers who have exposure to regulatory writing as well as hands-on experience of writing on medical devices or CER writing experience, and who aspire to be part of a world-class delivery team, and work in an exciting, fast-paced global environment.

As a CER writer in the CACTUS Medical team, you will:

• Ensure timely production of high quality CERs for devices across therapeutic areas
• Screen and summarize literature for relevant clinical data
• Review literature to elucidate the clinical problem and current treatment techniques
• Study and report device characteristics and instructions for use
• Evaluate data for similar competitor devices
• Summarize post-marketing surveillance and risk management data for the target device
• Work with senior writers to prepare documents that meet client expectations in terms of content, format, and presentation

Location: Andheri (West)
Qualification:

• PhD (preferably in the pharmaceutical sciences)/MBBS/MD with knowledge of clinical research, and first-author publications in international peer-reviewed journals. 
• A Masters degree with clinical research exposure and significant publications experience can also be considered. 

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Research Associate/ Scientist- Clinical Affairs F&D@ Alembic Research - 1 Opening(s) -Alembic Pharmaceuticals Limited

Job Description
 1. Responsible for clinical study monitoring, preparation of SIV, SMR for all periods, SCV for BA/BE studies.
2. Prepare, organize, conduct and follow-up site evaluation visits, site initiation visits, routine monitoring and close out visits as per relevant study plan
3. Verify quality, accuracy of data. efficient resolve data and audits queries and issues
4. Adhere to the study protocol and study procedures manual, complete all reports accurately and within the predetermined timelines
5. Review of study related documents, maintaining the project files and records for regulatory audits.
6. Responsible for maintaining study files (TMFs) at sponsor site.
7. Responsible for review of Clinical study report
8. Well versed with regulatory requirement USFDA, EMEA, ANVISA, Health Canada, DCGI, CDSCO w.r.t BA/BE and clinical studies.
9. To assist team in CRO selection as per the SOP, quality and regulatory standards.
10. To coordinate effectively with all stakeholders (PM, regulatory department, BE center, Plant QA) for smooth conduct of clinical studies.
11. Adherence to ICH-GCP and any other regulatory guidelines and requirements including adverse events and serious adverse event reporting
12. Compliance with mandatory SOPs as agreed for the study.
13. Good communication skill and Performs other duties as assigned.

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Clinical Research Coordinator TECH OBSERVER

1 - 2 yrs , Mumbai , Ludhiana , Bengaluru/Bangalore

 

Job Description

Recruitment,coordination & follow up of trial subjects, covering informed consent, adhering to safety and compliance issues;sample collection & shipment;Administer study drug;Coordination & management of Clinical Trial;

Salary:INR 1,25,000 - 2,00,000 P.A
  

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Contracts Analyst ( Clinical Research Experience )

 

 

PURPOSE

Under general supervision, develop and prepare contracts for assigned customers, to support the Global sales team.

RESPONSIBILITIES

Work closely with project teams to determine appropriate terms and conditions of contracts

Develop and prepare Contracts

Act as primary customer interface on small to mid size projects

Support senior team members on medium to larger customers / projects

Revise or develop contract and related budgets and scope of work. Ensure the scope of work is defined correctly and

budgets reflect the scope. Ensure any changes are integrated into the main study contract efficiently and accurately

Assist in the negotiation of legal contracting text using Quintiles Global Contracting Policy, templates and fallbacks

Oversee finalization and distribution of documents

Update and maintain contract databases and files

Perform all other duties as assigned

All responsibilities are essential job functions unless noted as nonessential (N).

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

Knowledge of CRO Industry

Knowledge of Microsoft Excel, Word and understanding of costing models

Possess strong analytical skills and excellent verbal and written communication skills

Ability to establish and maintain effective working relationships with coworkers, managers and customers

.

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

Degree in Life Science, Business Management or related field and a minimum of 2-3 year's direct experience in contracts

or equivalent combination of education, training and experience

PHYSICAL REQUIREMENTS

Extensive use of telephone and face-to-face communication requiring accurate perception of speech

Extensive use of keyboard requiring repetitive motion of fingers

Regular sitting for extended periods of time

Occasional travel

 APPLY ONLINE

 

 

Next-Generation Orphan Drug Delivery Ebook

According to the National Organization for Rare Disorders (NORD), a disease is rare if it affects fewer than 200,000 Americans. Big Pharma used to ignore this segment of the market, but now developing orphan drugs to treat these rare diseases is an industry priority. Driving efficient timelines is a key to bringing products to market on an accelerated track. If you don’t have formulation, analytical, clinical, and manufacturing resources and infrastructure in-house, maintaining a development programs that takes full advantage of an expedited designation from the FDA can be challenging.

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Biocon: IPO will evolve Syngene CRO into full manufacturing services firm

Indian CRO Syngene has received approval for its IPO prospectus paving the way to spin out from its parent company Biocon.

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India mulls reclassifying vitamins as drugs if they come with health claims

India may classify vitamin supplements as drugs rather than foods if the manufacturers of such products claim they can treat or prevent disease.

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Indian government task force calls to simplify clinical trial approval process

As the number of approved clinical trials in India continues to taper off compared to years past, a government task force is now calling for a new expedited trial approval process. 

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Viral Clearance for Biopharmaceuticals

Viral clearance studies are mandated prior to entering clinical trials and for commercial launch of biopharmaceuticals.  These studies are a key component of risk mitigation to reduce the potential for iatrogenic transmission of pathogenic viruses. This paper reviews regulatory guidance and practical strategies for designing viral clearance studies.  Essential elements for a developmental phase-appropriate viral clearance package are detailed.

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NDA for first tablet with stomach-activated digital sensor

A Japanese company has filed the first US FDA application for a drug with an embedded sensor which can tell doctors if patients have taken their pills.

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Top three reasons to go further with MPI Research

Cardiovascular disease, which includes coronary and peripheral artery disease, stroke,myocardial infarct and congestive heart failure, continues to be the leading cause of death worldwide. Despite the clear potential for impacting human health, drug discovery and device development in this area has been hampered by challenges in developing predictive preclinical models for use in evaluating the efficacy and safety of potential therapeutics. Furthermore, the extensive range of techniques, models, and assessments relevant for drug or device development in this space required expertise with these models and can be time consuming. Read More