Amaan AnsariCompleted B Pharm from North Maharashtra UniversityHaving 3.5+ years of experience in Clinical data managementOn a personal front, I am keen to help and guide individuals in clinical data management and pharmacovigilance.Also on general aspects such as communication skills, inter personal skills, interview tips, Resume Writing, Email Writing etc…
Centralized monitoring is a remote evaluation of the study data, carried out by a team including central monitors, and medical reviewers at a location other than the sites at which the clinical investigation is being conducted. The major difference between CRA monitor and centralized monitor is onsite monitoring and centralized monitoring…
This article is posted from https://www.linkedin.com/pulse/clinical-data-management-basics-freshers-pharmatech-life/ Clinical data management (CDM) is one of the most popular fields in clinical research. Many of the freshers and even experienced want to pursue clinical data management jobs. In the article on how to start a career in clinical data management, we discussed the groundwork…
Ministry of Health and Family Welfare [MoHFW] has notified the “New Drugs and Clinical Trials Rules, 2019” on 25th March 2019 [Ref Ministry of Health GSR Notification #227 dated 19 March 2019].
After reviewing CVs/Resume and one-to-one conversations with entry-level candidates, Sharing my insights for applying at Entry-level jobs in clinical trials.
Career goals or resume goals act as the tone of your resume. It spells out your career goals and objectives. This article is in line with the clinical trial candidates and professionals.
ISF plays a critical role in a study’s success. The investigator site file is consists of trial documents from the initiation to closeout. Ma
Aman is a pharmacy graduate and he finds the perfect job opening which matches his role. He prepared the perfect resume along with
Informed Consent is the process of consenting for the protection of human subjects in clinical research require that an investigator obtain the
Craig Lipset Clinical Trial Innovator • Board Member • Adviser • Investor • Educator • Speaker • Advocate
Hello!A well written resume or CV will highly impact your job hunt. I am not resume review expert but I guide freshers and professionals on the basis of my experience in clinical research and analysis of recruiters requirement. When I write about analysis, it covers skills, introduction, grammar, powerful language…
Aim Clinical trials are research studies performed in people that are aimed at evaluating a medical, surgical, or behavioural intervention. They are the first way that researchers determine if a replacement treatment, sort of a new drug or diet or medical device is safe and effective in people. Clinical Trials…
Before clinical trials, tests and coverings are assessed in preclinical research. Preclinical research is not done with people. It assesses the features of a test or treatment. For example, the research may aim to find out if a tool is harmful to living tissue. Let's read about the clinical trial…
Bioequivalence studies are very important for the development of a pharmaceutical preparation in the pharmaceutical industry.
The COVID-19 pandemic has caused disruption to clinical trials around the globe. Although, sponsors, CROs, clinical trial sites and other stakeholders are continuing their crucial work. But the question is Is COVID-19 Impacting Clinical Trials in India? Novel coronavirus impacted on patient recruitment for new trials and to keep already-enrolled…
Hi, I am Pooja Madhukar Parab. I am Msc bioanalytical scientce graduate. I am CRC at Tata Memrial Hospital, Mumbai.
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