Unlike the past traditional situations (production industries) there are many opportunities in the pharma field like

• Clinical Trial Management: Clinical Research Coordinator, Clinical Research Associate, IEC assistants, Digital Patient counselling, Clinical Data Coordinators, eTMF management, etc ….jobs are available.
• Clinical Data Management: Clinical Data Analyst, SAS programmer, Clinical Data Designers, etc…
• Pharmacovigilance: Drug Safety Associates, after gaining experience you can become Sr DSAs, Quality Control Reviewers, Subject Matter Experts and Team Leads.
• Regulatory Affairs and Medical Writing are the most booming career nowadays.

Yes, there are ample opportunities for career advancement in clinical research, including moving into higher-level roles with greater responsibility, specializing in a specific area of research or therapeutic area, pursuing leadership positions, obtaining additional certifications or advanced degrees, and transitioning to roles in academia, industry, or regulatory agencies.

What:   Pharmacovigilance course is to train you on the basic concepts (to make you understand the PV process, ethics, and jargons, etc….)

Why:   By learning these courses you will be familiarised to the PV profession and the course knowledge definitely reflects on your job role. You can see the difference between the very freshers who are not having the PV course knowledge.

Where:   Certified PV course is offering the by the institutions like IACR institute.

What:   The science and activities relating to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems.

Why:   PV activities can be done to assess the benefit, harm, effectiveness, and risk of medicines, encouraging their safe, rational and more effective use.

Where:   PV activities are conducting in Sponsor’s site, MNCs, IT companies, CROs and AMCs also.

When:   It was started in the 1960s but from 2007 onwards its running efficiently.

Enroll for our demo sessions, All your questions will be answered.

Our placement in charge and trainers will help you on applying and shortlisting for an interview

If you spend a minimum of 2 years you can get good recognization in any other company.

Aptitude to crack the interview, developing your interpersonal skills, good knowledge in clinical research , problem solving skills, scenario-based examples. Inter departmental knowledge! Look into our curriculum ! We have covered all essential requirements.

Participation in a clinical study means you will work with a research team in a medical setting. Team members include doctors, nurses, study coordinators, and other health care professionals. A principal investigator monitors participants during the research study. How the study will be conducted will be explained to you during the consent process.

Clinical Research and Pharmacovigilance are the inter-related branches and CR is the basic foundation of PV. You can play efficient Drug safety associate role if you have Clinical research experience.

In CR the PV activities can be performed but in normal level, bcoz we will control the situations up to one level by setting Inclusion and Exclusion criteria, whereas in Post Marketing Survivalence we will see a wide range of PV activities as various unrestricted conditions support unexpected Adverse Drug Reactions.

Clinical trials for new medications will often list a "phase" in their description. Here is what those phases indicate:

• Phase 1: This is an study in a small group of 20 to 80 people in which researchers evaluate the drug's safety, determine how it works in the human body. It also identifies side effects and is used to determine a safe dosage.
• Phase 2: This study looks at how effective the drug is in a slightly larger group of people, generally between 100 to 300. Further safety evaluations are also done at this phase.
• Phase 3: A phase 3 study is done after early evidence suggests the drug is effective. This is an expanded trial that includes thousands of people, both those taking the medication and people not taking it. It is used to confirm effectiveness, monitor side effects, and compare the new drug to commonly used treatments for the same condition. 
• Phase 4: These studies are done after the drug has been marketed. They are done to collect information about the drug's effect in specific populations, and to measure any side effects associated with long-term use.

As there is no specific degree for Clinical research from the universities to pursue a career in this competitive world one should require CR certification. IACR is providing excellent training with placement assistant. So don’t miss out to enhance your career.

Be proactive, persistent, and open to new opportunities. Utilize online job portals,  Network with professionals, Reach out to recruiters,  Tap into your educational institution like us ,  Consider internships and volunteer opportunities. s?

As per Salary.com, a CRA in United States earns a median base salary of $85225 where as a Clinical Research Manager earns $101,309, almost double of the CRA wages. The median annual salary for a Clinical Research Director is quoted between $118,518–$161,776. As per sources, in India, the average salary range of clinical research professionals is between INR 3 lacs p.a (CRA) to INR 25 lacs (Clinical Research Director).

Clinical Research after dentistry is like a new feather in cap which will come with its host of advantages. You may opt for a fellowship program or MSc in Clinical Research. By doing this, you will gain both in terms of job satisfaction and professional income as your clinical research degree opens up a plethora of fascinating job opportunities for you. As a dentist, this will hone your professional skills further and help you not just indulge in dental treatments and procedures but also devise and innovate improved ones through extensive research and clinical trials.

Designed to help you create a seamless onboarding experience for the students, ensuring the initial steps of the induction part are taken forward.