...needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing develo...
...About the job
The clinical lead will work with the senior clinical Lead and the Head of clinical function to design the clinical development plan and finalize the development strategy for Phase II and Phase III t...
...TCS is hiring for Content Specialist professionals!
Role: Medical writer
Work location: Mumbai
Experience: 8 - 13 years’ relevant experience in Medical writing
Qualification: Any Life science Graduate ...
...recruitment and trial awareness.
• Assess the clinical feasibility of implementing a clinical trial protocol based on regional/local medical practice using physician interviews, local databases (RWE, payer data, p...
...documents we authored last year. As an Expert Regulatory Writer, you will develop documents which cover all Novartis therapeutic areas and therapies, ranging from Phase I to IV Clinical Study Reports to regulatory s...
...consumer healthcare companies. Our services include investigator sites across India, risk-based remote monitoring and project management, medical writing, data publication, regulatory submissions. Our experienced te...
Urgent requirement Junior and Senior Embryologist to join IVF (In Vitro Fertilization) Center in Saudi Arabia
Job Overview:
Embryologists will be responsible for the handling, assessment, and manipulation of gametes (sperm and eggs) and embryos...
...As an Expert Regulatory Writer, you will develop documents which cover all Novartis therapeutic areas and therapies, ranging from Phase I to IV Clinical Study Reports to regulatory submission documents (e.g. Clinica...
...As a Clinical Researcher, Your Main Responsibilities Are
Design and conduct clinical trials in the skin category such as Acne, Pigmentation, Atopic Dermatitis, Skin hydration, Skin Barrier function Anti-ageing.
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...recruitment and trial awareness.
Assess the clinical feasibility of implementing a clinical trial protocol based on regional/local medical practice using physician interviews, local databases (RWE, payer data, pa...