Company Description Jehangir Clinical Development Centre (JCDC) is a global, clinical-stage full-service CRO providing comprehensive support for Phase I-IV clinical trials, validation studies, real world evidence (RWE) studies, and biobanking projects. With over 350 successfully executed clinical projects, JCDC has a proven track record in developing pharmaceutical, biotechnological, nutraceutical, and medical device products. Our expertise spans medical writing, monitoring, project management, clinical data management, regulatory support, biostatistics, and site management. JCDC is ISO 9001:2008 certified and accredited by AAHRPP, and has been recognized as the Best Investigator Site by the Indian Society of Clinical Research. We are dedicated to clinical precision in all our endeavors. Role Description This is a full-time role for a Medical Writing Associate, based in Pune. The Medical Writing Associate will be responsible for authoring and reviewing clinical research documents, including protocols, investigator brochures, clinical study reports, and regulatory submission documents. The role entails collaborating with cross-functional teams to ensure the accuracy and clarity of documents and ensuring compliance with regulatory guidelines. Additionally, the Medical Writing Associate will conduct literature reviews, interpret clinical data, and contribute to scientific publications. Qualifications Excellent written and verbal communication skills Attention to detail and ability to work independently and in a team Proficiency in medical writing and familiarity with regulatory guidelines Master's or Doctoral degree in a relevant field such as Medicine, Life Sciences, or related discipline Experience in clinical research or a CRO is a plus
Company Description Jehangir Clinical Development Centre (JCDC) is a global, clinical-stage full service CRO dedicated to delivering end-to-end services for Phase I-IV clinical trials, Validation studies, Real World Evidence (RWE) Studies, and Biobanking projects. With over 350 successfully executed clinical projects, our expertise spans multiple therapeutic products including Pharmaceuticals, Biotechnological, Nutraceutical, Herbal, and Medical Devices. JCDC is the first and only hospital-based research center in India to be ISO 9001:2008 certified and accredited by AAHRPP. Recognized for its excellence, JCDC was awarded the Best Investigator Site by the Indian Society of Clinical Research. Role Description This is a full-time role for a Clinical Data Management Associate at our Pune location. The Clinical Data Management Associate will be responsible for reviewing clinical data, managing data processes, validating data entries, and ensuring the accuracy and integrity of clinical data throughout the trial lifecycle. Day-to-day tasks will include data review, clinical data management, data validation, and collaborating with other teams to support clinical and regulatory requirements. Qualifications Skills in Clinical Data Review, Clinical Data Management, and Data Validation Experience with data management processes and clinical data handling Strong attention to detail and accuracy in data review Excellent organizational and time management skills Ability to work effectively in a hybrid work environment Bachelor's degree in Life Sciences, Data Management, or related field Previous experience in a clinical research environment is a plus