Clinical Research Physician
Company Description
GRG Health, part of the Growman Group of Companies, is a fast-growing healthcare research firm with offices across India, United Arab Emirates, the Philippines, Singapore, United Kingdom and the United States. Specializing in global life sciences, GRG Health provides healthcare intelligence through innovative, technology-driven solutions, including AI and machine learning. Supported by a team of over 300 analysts, GRG Health has garnered recognition as the "Most Innovative Healthcare Research Company in Asia 2020" by CEO Magazine. Dedicated to digital transformation and process optimization, GRG Health delivers cutting-edge insights to enhance healthcare services worldwide. Role Description The Clinical Research Physician will support healthcare research projects by providing clinical and scientific expertise, with a particular focus on interpreting data and validating medical insights. This part-time, remote role involves reviewing research protocols, assessing clinical trial information, and contributing to the design and evaluation of studies across various therapeutic areas, including oncology. The physician will collaborate with analysts and project teams to ensure medical accuracy, relevance, and compliance with clinical standards in all deliverables. Responsibilities include offering medical affairs input, reviewing literature and clinical data, participating in internal discussions on study outcomes, and helping translate complex clinical concepts into clear, actionable intelligence for life sciences clients.
Qualifications
Strong grounding in Medicine, with a valid medical degree (MD, MBBS, or equivalent) and clinical practice experience. Experience in Medical Affairs, including medical review, scientific communication, and clinical input into research or commercial projects. Demonstrated Research experience, such as literature review, data interpretation, and contribution to clinical or observational studies. Exposure to Clinical Trials, including understanding of study design, endpoints, protocols, and regulatory/ethical considerations. Specialization or significant experience in Oncology, or strong interest and familiarity with oncology clinical data and treatment landscapes. Excellent analytical and critical thinking skills, with the ability to interpret complex clinical information and provide clear recommendations. Strong written and verbal communication skills in English, with the ability to collaborate effectively in remote, cross-functional, and global teams. Comfort with digital tools and platforms; prior experience working in technology-enabled or data-driven environments is an advantage. Previous involvement in healthcare research, health economics/outcomes research, or pharmaceutical/biotech consulting is beneficial.