Clinical Trial Associate

**Clinical Trial Associate**: Gurgaon, Haryana **Job ID** R0120735 **Category** Research & Development **Subcategory** Research & Development **Business Unit** Global Portfolio Division **Job Type** Full time **OBJECTIVES**: - _Perform day-to-day management of CTMS and eTMF, including oversight of the review and approval of eTMF documents and...

Clinical Trial Responsibilities - Assist investigator site activation activities, including compilation and submission/notification of regulatory documents. - Assisting Trial Capabilities Associate on study document management & tracking for IRB/IEC submissions throughout the study. - Track site compliance to required training to effectively drive timelines...

**Clinical Trial Coordinator**: Under the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as...

We are currently looking for passionate, and committed professional to join our team as Research associates. B. Pharm, M. Pharm with work experience and/or Post Graduate Diploma in clinical research, preferred. The ideal profile will have 0.5- 2 years of experience. An equivalent combination of education, training and experience may be accepted in place of a...

We are currently looking for passionate, and committed professional to join our team as Research associates. B. Pharm, M. Pharm preferred or Bachelor's Degree in a Life Sciences discipline or health care, with Post Graduate Diploma in clinical research. The ideal profile will have 0.5- 2 years of experience. An equivalent combination of education, training...

We’re looking for people who are determined to make life better for people around the world. The Trial Capabilities Manager provides clinical trial capabilities in support of clinical development. The Manager is accountable to ensure the investigator sites meet requirements to enroll study participants into clinical trials and support ongoing...

We’re looking for people who are determined to make life better for people around the world. The Trial Capabilities Manager provides clinical trial capabilities in support of clinical development. The Manager is accountable to ensure the investigator sites meet requirements to enroll study participants into clinical trials and support ongoing...

We’re looking for people who are determined to make life better for people around the world. The Trial Capabilities Manager provides clinical trial capabilities in support of clinical development. The Manager is accountable to ensure the investigator sites meet requirements to enroll study participants into clinical trials and support ongoing...

We’re looking for people who are determined to make life better for people around the world. The Trial Capabilities Manager provides clinical trial capabilities in support of clinical development. The Manager is accountable to ensure the investigator sites meet requirements to enroll study participants into clinical trials and support ongoing...

Responsibilities : Oversight of CRO / other vendors and study management- Oversees CRO pre-site selection and site initiation, interim close-out and co-monitoring visits to ensure compliance with protocol and regulatory requirements and to assure good site performance Assists in the management of CROs and other vendors to ensure project requirements...

Responsibilities : Oversight of CRO / other vendors and study management- Oversees CRO pre-site selection and site initiation, interim close-out and co-monitoring visits to ensure compliance with protocol and regulatory requirements and to assure good site performance Assists in the management of CROs and other vendors to ensure project...

**Description** **Central Report Reviewer** Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient...

Job Summary RTL/Sr. RTL is responsible and accountable for deliveries of studies allocated to RCO unit, performing end to end study related project management for studies managed in-house with-in agreed timelines, budget and desired quality standards. For Outsourced study, RTL/Sr. RTL will be responsible to provide an efficient Sponsor Oversight and...

**Title**:Manager-1-Clinical Quality & Process**: - Date: May 3, 2024- Location: Gurgaon - R&D- Company: Sun Pharmaceutical Industries Ltd**Job Purpose** The Clinical Process and Quality Manager (CPQM) is primarily responsible to support all Global Development (GD) functions for ensuring audits and inspection readiness through periodic quality control...

**Job Purpose** The Clinical Process and Quality Manager (CPQM) is primarily responsible to support all Global Development (GD) functions for ensuring audits and inspection readiness through periodic quality control activities. **Key Roles and Responsibilities** - Acts as Quality Partner for assigned Global Development Functions and drives Quality...

Job Purpose: Principal Clinical Study Manager is at the heart of our Evidence Generation activities and aligned to our Cultural pillars of Go Beyond, Do What Matters Most and Keep it Human. The role provides operational leadership to the Clinical Study Team and is responsible for the planning, management, execution, and delivery of the trial...

Job Purpose: Principal Clinical Study Manager is at the heart of our Evidence Generation activities and aligned to our Cultural pillars of Go Beyond, Do What Matters Most and Keep it Human. The role provides operational leadership to the Clinical Study Team and is responsible for the planning, management, execution, and delivery of the trial...

Hi, We are hiring for **Healthcare Research Associate **profile for **Gurgaon** Location please find the job responsibility as below: - **Job Title**: Healthcare Research Associate **Experience ** : 0 month to 3 years **Location**: Gurgaon Sector-18 **Working Days ** : Monday To Friday **Shift Timings ** : Rotational Shift Depends on projects - **2:00 PM...

Job Purpose: Principal Clinical Study Manager is at the heart of our Evidence Generation activities and aligned to our Cultural pillars of Go Beyond, Do What Matters Most and Keep it Human. The role provides operational leadership to the Clinical Study Team and is responsible for the planning, management, execution, and delivery of the trial...

Job Purpose: Principal Clinical Study Manager is at the heart of our Evidence Generation activities and aligned to our Cultural pillars of Go Beyond, Do What Matters Most and Keep it Human. The role provides operational leadership to the Clinical Study Team and is responsible for the planning, management, execution, and delivery of the trial...