Interested to become part of team revolutionising the Medical Anatomy Study!
Cofounded by graduates from IIT KGP, DCE and IIM A, Immersive Labz works on cutting-edge medical technology, specialising in creating immersive v...
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical develop...
...trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborat...
...trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborat...
Interested to become part of team revolutionising the Medical Anatomy Study!
Cofounded by graduates from IIT KGP, DCE and IIM A, Immersive Labz works on cutting-edge medical technology, specialising in creating immersive v...
...custodian.
Compilation and Archival of clinical raw data.
Preparation of various solutions, Labels.
Measuring Height and Weight of Volunteer.
Registration of Volunteers.
Screening of Volunteers.
Pe...
...Fortrea is transforming drug and device development for partners and patients across the globe.
Assist in the processing of Expedited Safety Reports (ESRs), Periodic Safety Reports (PSRs) and submission, includin...
...reports reported either spontaneously from any source or from a clinical trial. This includes, but is not limited to:
Data entry of safety data onto adverse event database(s) and tracking systems
Review of adv...
...research field Experience: 2-5 years
Note: Bioequivalence, Bio-Availability studies (BA/BA) Mandatory Experience
Job Description For Medical Writer
Preparation of BA/BE study protocol in compliance with IC...
...The Clinical Scientist is responsible for medical writing activities at Innovaderm. The individual will author or contribute to development of clinical and regulatory documents (synopsis, study protocols, statistica...
