Full Time
Responsibilities • Oversee and manage clinical research projects within the Regulatory Affairs department, ensuring compliance with all regulatory requirements. • Coordinate with cross-functional teams to facilitate smooth progression of research act
Full Time
Responsibilities • Assist in the coordination and management of clinical trials conducted by research organizations. • Ensure compliance with regulatory requirements and ethical standards throughout the research process. • Maintain accurate and up-to
Full Time
Responsibilities • Assist in the coordination and management of clinical trials conducted by research organizations. • Collaborate with principal investigators and study teams to ensure timely execution of study protocols. • Maintain accurate and com
Full Time
Responsibilities • Conduct innovative pharmaceutical research to contribute to scientific advancements. • Collaborate with research teams to design and implement experimental protocols. • Analyze data and interpret results to draw meaningful conclusi
Full Time
Responsibilities • Conduct innovative research in pharmaceutical development to advance scientific knowledge and support company objectives. • Design, execute, and analyze experiments, ensuring accuracy and precision in research methodologies. • Coll
Full Time
Responsibilities • Manage, coordinate, and oversee the entire data management process for clinical trials, ensuring high-quality data collection and data integrity. • Develop and implement data management plans, including data entry, validation, and
Full Time
Responsibilities • Conduct comprehensive analysis and research to develop and validate analytical methods for pharmaceutical products. • Collaborate with cross-functional teams to support the formulation and development of new drug products. • Perfor
Full Time
Design, establish, and validate in vivo models of fibrosis across key organs like lung, liver and Kidney Independently plan and conduct in vivo efficacy, PK/PD, and mechanistic studies in rodent models Develop detailed study protocols, animal handlin
Full Time
<strong>RESPONSIBILITIES:</strong> · Design and develop analytical methods for drug substances and drug products (oral solid dosage forms and/or injectables) in compliance with regulatory requirements for global markets (USFDA, EMA, etc.). · Perform
Full Time
Responsibilities • Oversee the management and analysis of clinical trial data to ensure accuracy and integrity. • Collaborate with clinical research teams to design and implement data management plans. • Develop and maintain databases for clinical tr
Full Time
Responsibilities • Conduct research to develop innovative drugs, formulations, and pharmaceutical technologies. • Collaborate with cross-functional teams to design and implement research projects. • Analyze data and document findings to support the d
Full Time
<strong>RESPONSIBILITIES:</strong> · Design and develop analytical methods for drug substances and drug products (oral solid dosage forms and/or injectables) in compliance with regulatory requirements for global markets (USFDA, EMA, etc.). · Perform
Full Time
Responsibilities • Lead and execute research projects in drug discovery, focusing on in-vitro biology. • Collaborate with cross-functional teams to identify and validate new drug targets. • Design, implement, and analyze experiments to support drug d
Full Time
Responsibilities • Oversee and manage the daily operations of the pharmacology department, ensuring alignment with company goals and regulatory standards. • Collaborate with cross-functional teams to develop and implement strategic plans for product
Full Time
Responsibilities: · Lead and manage Analytical Development activities for drug substances and drug products (OSD and/or injectables) for regulated markets (USFDA, EMA, etc.) · Provide technical guidance on analytical method development, validation, a
Full Time
Scientist I - Product development (Formulation R&D) will be responsible for leading formulation development activities, managing a portfolio of projects, and ensuring successful product development and regulatory submissions for global markets. The r
Full Time
Designation: Regulatory Affairs Specialist Location: Hyderabad (On-site) At Aodh Lifesciences, we are building a next-generation deep science drug development company focused on redefining respiratory drug delivery through a regulatory-driven approac
Full Time
▪ Develop and execute regulatory strategies and plans to ensure compliance with applicable laws, regulations, and standards. ▪ Stay updated on changes in regulatory requirements and translate them into actionable steps for the organization. ▪ Collabo
Full Time
Responsibilities • Conduct research and development activities focusing on the design and synthesis of novel compounds for drug discovery. • Collaborate with cross-functional teams to optimize lead compounds and enhance drug efficacy and safety profi
Full Time
Responsibilities • Assist in the management and care of geriatric patients under the supervision of senior healthcare professionals. • Support daily clinical operations within the general department, ensuring patient comfort and safety. • Participate
Full Time
Scientist IV - Product development (Formulation R&D) will be responsible for leading formulation development activities, managing a portfolio of projects, and ensuring successful product development and regulatory submissions for global markets. The
Full Time
Responsibilities: · Conduct patent searches, invalidity searches, and patent landscape analysis for pharmaceutical products and technologies. · Evaluate innovator patents, Orange Book patents, and exclusivity status for ANDA / 505(b)(2) product devel
Full Time
Responsibilities • Provide expert advice on drug development processes to ensure alignment with industry standards and best practices. • Guide pharmaceutical companies in understanding and navigating regulatory requirements and compliance issues. • C
Full Time
Responsibilities • Conduct thorough analysis of pharmaceutical products to ensure quality control and regulatory compliance. • Perform both routine and non-routine testing in private laboratory settings. • Collaborate with the laboratory team to deve
Full Time
Responsibilities • Promote and sell pharmaceutical products to healthcare professionals, ensuring a clear understanding of product features and benefits. • Develop and maintain strong relationships with healthcare professionals to encourage product e
Full Time
Responsibilities • Prepare and develop high-quality scientific documents, ensuring accuracy and clarity. • Collaborate with research teams to gather and interpret clinical data for regulatory submissions. • Draft, edit, and review research publicatio
Full Time
Responsibilities • Provide expert diagnostic imaging services and interventional radiology procedures with a focus on GI, neuro, or cardiovascular systems. • Collaborate with multidisciplinary teams to ensure comprehensive patient care and optimal tr
Full Time
Responsibilities • Oversee the implementation and enforcement of drug control regulations within the pharmaceutical sector. • Ensure compliance with legal and ethical standards in the manufacturing, distribution, and sale of pharmaceutical products.
Full Time
Designation: Quality Assurance Specialist Location: Hyderabad (On-site) At Aodh Lifesciences, we are building a next-generation deep science drug development company focused on redefining respiratory drug delivery through a regulatory-driven approach
Full Time
Key Responsibilities 1. Clinical Strategy & Portfolio Ownership (Anti-Aging) Own and drive the strategy for Daulcel’s entire anti-aging portfolio, including IV therapies, injectables, nutraceuticals, and clinical skincare Ensure all products, protoco
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