2.0 - 6.0 years

0 Lacs

hyderabad, telangana

On-site

Role Overview: As a Regulatory Medical Writer-Clinical trials (RMW-CT), you will be responsible for providing regulatory affairs (RA) strategic document expertise and support to one or more therapeutic areas (TAs) designated by leadership. Your role will involve supporting the preparation and submission of critical RA documents and responses to health authority (HA) or sponsor information requests. You will be the lead contact for sponsor or designated HA interactions with cross-functional teams, ensuring the accuracy and quality of submission-ready documents. Key Responsibilities: - Serve as the regulatory lead representative on project teams, partnering with outsourcing and operational tea...

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Assistant Professor - Statistics DIT UNIVERSITY

2.0 - 8.0 years

0 Lacs

dehradun, uttarakhand

On-site

The ideal candidate for this position should possess the educational qualifications as prescribed by the respective Council/UGC. Preferential consideration will be given to candidates holding a Ph.D. degree. Candidates should have a minimum of 2-8 years of experience in Teaching, Industry, Research Organizations, or at a Professional Managerial level, excluding the time spent on obtaining their research degree. Additionally, candidates should have a minimum of 2 research papers published in peer-reviewed refereed Journals. Interested candidates are encouraged to submit their applications through the DIT University website. ,

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