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Post Graduation Diploma In Clinical Research ( 4.5 Month's )

Dive into Advanced clinical research Live Hands on Training Leading Software’s used in the Clinical Research Industry that add Additional Internship Experience for Your Corporate Career.

The curriculum is designed to meet the needs of the clinical research industry, with input from industry experts and stakeholders. Graduates are prepared for various roles within the pharmaceutical, biotechnology, medical device, and contract research sectors. Some programs may be accredited by professional organizations or regulatory bodies, and graduates may have the opportunity to pursue certification exams to further enhance their credentials.

ELIGIBILITY :

  • Any Medical, Paramedical, Pharmacy and Life Science – Graduates and Post Graduates
  • Nursing, B.Pharm, M.Pharm, PhD
  • Biotechnology / Microbiology/Biochemistry /Zoology /Anatomy /Physiology /Bioinformatics /Health Education/Lab Technician/Chemistry/Biomedical etc.
  • 4th/6th year B.Pharm/Pharma D students and 2nd year M.Pharm/M. Sc Students are also eligible
  • BPT, MPT, PHD, DIPLOMA IN PHARMACY
  • BDS, MDS, MBBS, BAMS, BHMS, BUMS MD, PHD
  • NURSING: GNM, BSC NURSING, MSC NURSING
  • B.TECH- BE: BIO INFORMATICS, BIOTECHNOLOGY, BIO MEDICAL ENGINEERING
  • HealthCare- Doctors, Researchers, Scientist's, PhD Holders
  • BACHELOR IN SCIENTIST'S, MASTERS IN SCIENTIST'S
  • Any Abroad University Affiliated Health Care Doctors | Doctor of Medicine

Future Demo Sessions:

Why wait when you can freely enroll and learn about Clinical research . We have a 1 hr Q & A session where all your questions related to Clinical research and your career will be answered by our expert trainers.

WEEKDAYS

09:00 AM & 6:00 PM

WEEKENDS

09:00 AM & 6:00 PM

Careers in Clinical Research :

A career in clinical trials offers a diverse range of opportunities for individuals interested in contributing to medical research and improving patient care. Here are some common career paths in the field of clinical trials:

  1. Clinical Research Coordinator (CRC) : CRCs are responsible for managing the day-to-day operations of clinical trials, including participant recruitment, informed consent, data collection, and regulatory compliance. They work closely with investigators, sponsors, and study participants to ensure that trials are conducted ethically and efficiently.
  2. Clinical Research Associate (CRA) : CRAs are involved in monitoring clinical trials to ensure that they are conducted according to regulatory requirements and study protocols. They conduct site visits, review study documentation, and communicate with investigators and study staff to ensure data quality and participant safety.
  3. Clinical Trial Manager (CTM) : CTMs oversee the planning, execution, and monitoring of clinical trials. They manage cross-functional teams, develop study protocols and timelines, and ensure that trials are conducted on schedule and within budget. CTMs play a critical role in ensuring the success of clinical trials from start to finish.
  4. Clinical Data Manager (CDM) : CDMs are responsible for collecting, managing, and analyzing clinical trial data. They design data collection forms, develop database systems, and perform quality checks to ensure data accuracy and integrity. CDMs play a crucial role in ensuring that trial results are reliable and valid.
  5. Clinical Trial Statistician : Statisticians work closely with researchers to design clinical trial protocols, analyze study data, and interpret results. They use statistical methods to determine sample sizes, analyze study outcomes, and assess the safety and efficacy of interventions. Clinical trial statisticians play a key role in ensuring that trials are statistically sound and produce meaningful findings.
  6. Regulatory Affairs Specialist : Regulatory affairs specialists ensure that clinical trials comply with regulatory requirements and guidelines set forth by government agencies such as the FDA. They prepare regulatory submissions, maintain documentation, and communicate with regulatory authorities to obtain approvals and ensure compliance throughout the trial process.
  7. Medical Writer : Medical writers prepare various documents related to clinical trials, including study protocols, informed consent forms, investigator brochures, and regulatory submissions. They translate complex scientific information into clear and concise language for diverse audiences, including researchers, regulators, and study participants.
  8. Clinical Trial Investigator : Clinical trial investigators are physicians or other healthcare professionals who lead clinical trials at research sites. They are responsible for overseeing all aspects of the trial, including participant recruitment, data collection, and safety monitoring. Investigators play a crucial role in advancing medical knowledge and improving patient care through their research efforts.

These are just a few examples of career paths in clinical trials. Depending on your interests, skills, and educational background, there are many other opportunities available in areas such as project management, quality assurance, patient recruitment, and bioethics. Whether you're passionate about conducting research, ensuring regulatory compliance, or communicating scientific findings, a career in clinical trials offers a rewarding opportunity to make a meaningful impact on healthcare and patient outcomes.

Frequently Asked Questions – FAQs

Clinical trials are the best way to study new, investigational treatments or vaccines to learn if they work and how safe they are. If you have ever taken medicine or gotten a vaccine, then you have benefited from clinical trials. Trials often try to answer specific health questions, like if a new treatment has any effect, if it could work better than an existing treatment, or if it’s safe for people to use. Some of these treatments have not been approved by a government agency, which is why they are called “investigational” treatments. If clinical trials show that a new treatment works and is safe, then it can be approved to be used by the people who need it.

The answer lies in clinical trials, meticulously designed research studies that test the safety and effectiveness of new healthcare interventions on human volunteers.

An introduction to clinical trial training is a perfect first step. This blog post will equip you with the foundational knowledge to jumpstart your journey.

The field of clinical research has seen a significant rise in demand over recent years. The evolving landscape of the pharmaceutical and biotechnology industries, with a constant push for new and improved treatments, plays a significant role in this growth.

You will be interview ready, as the certification program has all the departments hands on training in clinical research domain. It will add value to your CV, and you will have complete end-to-end exposure to the clinical trials and different departments in the clinical research industry.

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

As a fresher you would require Mathematics, English and logical thinking to clear the 1st round of the interview. So, we train you very well with all required aptitude requirements!

This training is valuable for anyone interested in a career in clinical research and any life science graduate.

Clinical study start up to study close out. Site selection, site initiation, site conduct and site close out!