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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