Research Associate/Senior Research Associate – Preclinical Biopharma

Job Description

Dear Aspirants,   Job Opening – Research Associate / Senior Research Associate Preclinical Biopharma – CRO | Efficacy & Toxicity Studies Location: Mahbubnagar, Telangana   Experience: 1–2 Years   Qualification: M.Sc. /M.Tech. /Ph.D. in Biotechnology, Life Sciences, Biomedical Sciences, or a related discipline   Industry: Biopharmaceutical CRO / Preclinical Research   We are looking for a highly motivated and technically competent candidate with 1–2 years of experience in a CRO or preclinical research environment to join our Biopharma Preclinical Research team.   Key Responsibilities   Ø Execute and support preclinical efficacy and toxicity studies for biopharmaceutical products. Ø Assist in in-vitro and in-vivo studies involving biologics, monoclonal antibodies, recombinant proteins, vaccines, and/or cell & gene therapy products. Ø Perform and support laboratory techniques such as: Ø Cell culture and cell-based assays Ø ELISA and other immunoassays Ø PCR/RT-qPCR Ø Flow cytometry Ø Western blot/IHC, where applicable Ø In-vitro cytotoxicity and functional assays Ø Assist with animal study procedures, dosing, sample collection, tissue processing, and study-related observations. Ø Support PK/PD, biodistribution, toxicity, and efficacy studies. Ø Maintain accurate raw data, study records, laboratory notebooks, and study documentation. Ø Work according to GLP/GCP principles, SOPs, study protocols, and applicable regulatory requirements. Ø Coordinate with study directors, scientists, animal facility personnel, and other CRO departments. Ø Assist in preparation of study reports, data summaries, and presentations. Desired Skills Ø Strong foundation in Biotechnology / Molecular Biology / Cell Biology. Ø Hands-on experience in mammalian cell culture and molecular biology techniques. Ø Exposure to preclinical CRO studies will be highly preferred. Ø Basic understanding of animal experimentation and preclinical study design. Ø Knowledge of GLP documentation and regulatory requirements is an advantage. Ø Good analytical, documentation, communication, and problem-solving skills. Ø Ability to work independently as well as in a multidisciplinary team. Ø Preferred Candidate Profile Candidates who have worked in a CRO, Biopharma, Biotechnology, or preclinical research organization and have exposure to efficacy, toxicity, PK/PD, biodistribution, or biologics-related studies are encouraged to apply. Interested candidates may share their updated CV with:   📧

Email ID: hr@palamurbio.com , mukesh@palamurbio.com