Associate Scientific Service (Medical Representative) San Fegan Biotech Private Limited

0.0 - 4.0 years

0 Lacs

chennai, tamil nadu

On-site

The Associate Scientific Service (Medical Representative) position at San Fegan Biotech Private Limited in Chennai is a full-time on-site role involving tasks related to scientific services and medical representation. As an Associate Scientific Service, you will be responsible for utilizing your strong communication and interpersonal skills to effectively engage with clients and healthcare professionals. Your knowledge of medical terminology and scientific principles will be essential in conveying technical information accurately and comprehensively. To excel in this role, you must possess the ability to build and maintain strong professional relationships with stakeholders. Attention to detail and organizational skills are crucial for managing and coordinating scientific service activities efficiently. While prior experience in the pharmaceutical or healthcare industry is advantageous, it is not mandatory. A Bachelor's degree in a relevant field is required to ensure a solid foundation for understanding and fulfilling the responsibilities of this position. If you are looking to leverage your scientific expertise and communication abilities in a dynamic and challenging environment, this role offers an exciting opportunity to contribute to the healthcare industry while further developing your skills and knowledge. Join our team at San Fegan Biotech Private Limited and be a part of our mission to provide innovative solutions and services in the field of healthcare.,

Posted 19 hours ago

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Clinical Database Programmer ProcDNA

3.0 - 7.0 years

0 Lacs

hyderabad, telangana

On-site

As a Clinical Database Programmer at ProcDNA, you will play a crucial role in designing the eCRF layout and corresponding database, implementing dynamic rules based on Sponsor requirements, and creating trial-specific Edit Checks. Your responsibilities will also include developing Custom Functions using C# for Rave studies or other EDC systems, incorporating internal and Sponsor feedback, and maintaining eCRFs and components as per protocol amendments or metadata updates. Additionally, you will support CRO trial activities, create reports using JReview, SAS, BOXI, and handle migration processes for Post Go-Live studies. To excel in this role, you must have a deep understanding of Clinical Protocol, medical and scientific principles of conducting clinical trials, and expertise in Critical Data Point Strategy (CDPS) or SDV implementation. Your strong writing, communication, research, and analytical skills will be essential in gathering, interpreting, and synthesizing data accurately. Attention to detail, project management capabilities, and the ability to manage a team are also crucial for success in this position. Ideally, you should be Certified in Medidata Study Builder (SDBE), Oracle - InForm/Central Designer, or Veeva Studio, with a background in Computer Science-based courses or Circuit Branches (B.E./B.Tech, M.Sc./MCA, B.Sc./BCA). Joining ProcDNA will offer you the opportunity to work in a fast-growing consulting firm that is making a real impact in the healthcare sector, collaborate directly with leadership, and contribute to shaping marketing strategies. Currently, we are seeking candidates for this role in Pune, Gurgaon, Bangalore, Kochi, Hyderabad, and Chennai. If you are passionate about database management, dynamic rules implementation, project management, and have a keen eye for detail, this role at ProcDNA could be the perfect fit for you. Apply now and be part of a team that values innovation, collaboration, and excellence in Commercial Analytics and Technology solutions.,

Posted 5 days ago

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