139 Job openings found

Job Description Exp in clinical SAS, exp in SDTM(Eagle/ARDS) Level 10/9 Location – Vikhroli Responsibilities/Authorities Review and analysis of source (raw) data. Author mapping specifications from source (raw) data to target (CDISC SDTM and/or sponsor defined standards). Develop CDISC SDTM domains utilizing a data conversion tool. Quality Control of CDISC SDTM domains. Create data definition files and Case ...

  Level 10 3.5 to 6.10years 7.5LPA to 13.5LPA NO . Of demands CL Role SLL Max Fixed CTC which we can offer 5 CL 11 CDM 17734-Data Maintenance-Clinical Data Management 732350 20 CL 10 CDM 22107-Data Maintenance-Clinical Data Management 998000 20 CL 10 CDM 27750-Data Maintenance-Clinical Data Management 998000 10 CL 10 PDM 31392-Clinical-Protocol Data Management PDM 998000   Role :   CL 10 Min 5 years exp Cl 11 Min 4 years exp   Location : Hyderabad Relocation : Can search for profiles PAN – India ...

MAIN PURPOSE OF ROLE  Experienced professional individual contributor that works under limited supervision.  Applies subject matter knowledge in the area of Medical Affairs.  Requires capacity to apply skills/knowledge within the context of specific needs or requirements.      MAIN RESPONSIBILITIES  As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.  Contributes to implementation of clinical protocols, and facilitates completion of final reports.  Recruits clinical investigators and negotiates study design and costs.  Responsible for directing human clinical trials, phases III & IV for company products under development.  Participates in adverse event reporting and safety responsibilities monitoring.  Coordinates and provides reporting information for reports submitted to the regulatory agencies.  Monitors adherence to protocols and determines study completion.  Coordinates and oversees investigator initiations and group studies.  May participate in adverse event reporting and safety responsibilities monitoring.  May act as consultant/liaison with other corporations when working under licensing agreements.    QUALIFICATIONS  Education – MD Pharmacology Experience/Background -  2 – 5years   

Overview The Head of Anaesthesia in the ICU for the Oncology Department plays a crucial role in ensuring high-quality anaesthetic care for patients undergoing oncological procedures. This position focuses on managing the anaesthesia services in the ICU, where the demand for specialized anaesthetic management for cancer patients is significant. The Head ...

Responsibilities: The Behavioral Therapist will provide clinical skills instruction and behavior reduction protocols based upon the principles of Applied Behavior Analysis to children with Autism and related developmental disabilities in clinic and community settings. The Behavioral Technician will collect data on programs, assist with parent training, and assist the Behavior Analyst, ...

Education and Experience Requirements/Qualifications:Base Level:• Bachelor’s degree or equivalent, preferably in Computer Science.• Minimum of 8 to 17 years’ experience building EDC databases in support of clinical research.• Technical EDC build experience using Medidata Rave.• Experience working on clinical trials.• Experience working in highly diverse teams within clinical research; cross-functional, ...

  Review of CRF Design against Protocol and Sponsor Specifications (SSPs). · Audit of database against the CRF to ensure compliance to Protocol, Regulatory requirements, In-house SOPs and SSPs. · Conduct audit of Clinical Data Management, Biostat and Programming, Consumer Research, and Software Development activities and communicate audit observations to the respective department. ...

Hi We have an opening for Medical Support for leading Pharma Company.   Position - Medical Support Work experience - 1 to 3 years Time - 9.00am to 6.00pm Job Description - Scientific Content Support Build strong relationships with key doctors and hospitals to share the latest medical and scientific updates on FreeStyle Libre and diabetes management. Develop and ...

1. NEW PRODUCT DEVELOPMENT RC grades to develop within 3 months time with commercial supply Other MCC combination product range to develop including MCC + Lactose, MCC Spheres,   Technical support including market complain to provide when & where is required Market support and explore to promote MCC, Powdered Cellulose ...

Qualification: Respiratory/Pain/Digestive Health/Skin Health: Bachelor's and Master’s in Pharmaceuticals/PhD/MBBS with relevant post-qualification experience in the scientific and business research space Oral Health: Bachelor's in Dental Sciences (BDS) or M.Pharm with Oral Care/ Consumer health experience. Good understanding of Dental Sciences with robust domain knowledge; clinical experience with deep understanding of the oral ...