Full-Time Clinical Provider

You will be a practitioner on our telehealth platform 'Intellect', where your role is to support our clients' mental health and personal growth based on the individual needs and goals. This is delivered primarily through scheduled 60-minute video sessions on our platform.This is a freelance remote role with the flexibility to decide your business hours....

Collaborate with clinicians, KOL to get the feedback and inputs on clinical trial design, comparator and endpoints of the study to finalize synopsis.Lead the clinical research medical science related activities such as preparation of synopsis, protocol, Clinical Study Report (CSR) and present the proposals in subjects expert committee (SEC) regulatory...

Job Title:Clinical Quality Assurance Compliance & trainingExperience: 5 plus yearsLocation:MumbaiType:Full-timeExperience Level:[Senior] Manager/Senior ManagerDepartment:Clinical Research DepartmentPurpose of this Role:This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective. This role will be accountable...

Job Title: Clinical Quality Assurance Compliance & training Experience : 5 plus years Location: Mumbai Type: Full-time Experience Level: (Senior) Manager/Senior Manager Department: Clinical Research Department Purpose of this Role: This role will be responsible for oversight on end-to-end clinical trial activities from quality...

Hiring for Clinical Science Lead - Medical Monitoring for a leading Pharma clientMumbaiTASKS AND RESPONSIBILITIESLead the clinical research medical science related activities such as preparation of synopsis, protocol, Clinical Study Report (CSR) and present the proposals in subjects expert committee (SEC) regulatory meetingCollaborate with clinicians, KOL to...

Position Title: Sr. Manager/ Manager Clinical Quality Compliance and TrainingYOUR TASKS AND RESPONSIBILITIES: This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective.This role will be accountable for Quality Compliance (QC) activities of Clinical Trial Medical Science team and Operations team, Clinical...

Summary -Responsible to support all statistical programming data review reporting and analytics development aspects of assigned studies or project-level activities Major accountabilities 1 Produce and track reports for various line functions within Global Drug Development used for ongoing monitoring of clinical data 2 Provide understandable and...

Summary Participate in the full lifecycle of producing key data and or reports in support of data review reporting development including evaluation of requirements design specifications interface to programmers report programming coordinate validation and rollout activities along with providing quantitative analytical support These tasks are to be...

**Job Summary**This is a full-time contract role offering 30–40 hours per week of consistent work. The contractor will act as a core member of the QA function, providing essential support to ongoing clinical programs and ensuring regulatory compliance.

Job SummaryOur clinical operations activities are growing rapidly and we are currently seeking a full-time Clinical Safety Manager to join our Clinical Safety Department in India This position plays a key role in the pharmacovigilance process at Medpace If you want an exciting career where you use your previous nursing or pharmacovigilance expertise and...