Clinical Investigator

Details: Role: IBR IBR Facility Reviewer/ Clinical Investigation Location: Hyderabad Shift Timing: Night shift (5:30 PM to 2:30 AM) Work Mode: 5 days from office Experience: 3-7 Years Skill Requirements: CPC Certification – Preferred but not mandatory; candidates with the certification will be given an added advantage. Experience in Denials and Clinical...

Details:- Role: IBR IBR Facility Reviewer/ Clinical Investigation- Location: Hyderabad- Shift Timing: Night shift (5:30 PM to 2:30 AM)- Work Mode: 5 days from office- Experience: 3-7 YearsSkill Requirements:- CPC Certification – Preferred but not mandatory; candidates with the certification will be given an added advantage.- Experience in Denials and...

Details: Role: IBR IBR Facility Reviewer/ Clinical Investigation Location: Hyderabad Shift Timing: Night shift (5:30 PM to 2:30 AM) Work Mode: 5 days from office Experience: 3-7 Years Skill Requirements: CPC Certification – Preferred but not mandatory; candidates with the certification will be given an added advantage. Experience in Denials and Clinical...

Details:Role: IBR IBR Facility Reviewer/ Clinical InvestigationLocation: HyderabadShift Timing: Night shift (5:30 PM to 2:30 AM)Work Mode: 5 days from officeExperience: 3-7 YearsSkill Requirements:CPC Certification – Preferred but not mandatory; candidates with the certification will be given an added advantage.Experience in Denials and Clinical...

Details:Role: IBR IBR Facility Reviewer/ Clinical InvestigationLocation: HyderabadShift Timing: Night shift (5:30 PM to 2:30 AM)Work Mode: 5 days from officeExperience: 3-7 YearsSkill Requirements:CPC Certification – Preferred but not mandatory; candidates with the certification will be given an added advantage.Experience in Denials and Clinical...

JOB DETAILS 1. Prevent the payment of potentially fraudulent and/or abusive claims utilizing medical expertise, knowledge of CPT/diagnosis codes, CMC guideline along with referring to client specific guidelines and member policies2. Adhere to the state and federal compliance policies and contract compliance 3. Assist the prospective team with special...

Optum is a global organization that delivers care, aided by technology to help millions of people live healthier lives. The work you do with our team will directly improve health outcomes by connecting people with the care, pharmacy benefits, data and resources they need to feel their best. Here, you will find a culture guided by diversity and inclusion,...

Hyderabad 02 to 06 Years Full Time - Plan and conduct investigator site selection audits and clinical trial study audits at investigator sites in accordance with applicable GCP guidelines and regulations. - Review of CRF design - Review of standard operating procedures - Issue audit reports to the investigator site staff and other concerned study personnel -...

Role & responsibilitiesAssist with the Ethics / Regulatory Submissions; keep a track of submissions & approvals for the study.Help medical team in preparing Protocols, Investigator Brochures and CRFs which includes keeping track and re-ordering supplies.Set up and maintenance of the Trial Master Files (TMF) or Electronic filing systems/ set up of the...

Details:Role: IBR IBR Facility Reviewer/ Clinical InvestigationLocation: HyderabadShift Timing: Night shift (5:30 PM to 2:30 AM)Work Mode: 5 days from officeExperience: 3-7 YearsSkill Requirements:CPC Certification – Preferred but not mandatory; candidates with the certification will be given an added advantage.Experience in Denials and Clinical...