Clinical Trial Protocol Specialist

We are looking for experienced Indian clinical trial disclosure associates to join our dynamic, collaborative team to engage with biopharmaceutical clients to prepare and maintain clinical trial registry postings across global registries. This a full-time, remote opportunity. **About Us** Kateric (a Propharma group company) is a strategic partner for...

Coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix. - Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system. - Ensures allocated tasks are performed on time, within budget and to a high quality standard. Escalates in cases of variances...

**Description** **Medical Writer II** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our customers...

**Job Title**: **Clinical SAS Programmer** **Job Location**: Anywhere in India (Remote)**Job Overview**: The Clinical SAS Programmer supports Clinipace data operations by providing programming services to Data Management. This position works under the supervision of a Senior Clinical SAS Programmer and/or management and will assist in various assigned...

SaphireX Surgicals is a Mumbai-based healthcare company that specializes in providing top-of-the-line surgical solutions through advanced navigation systems. The company has recently launched its innovative product named NeuroSAPHIREX, a Neuronavigation system that is designed to enhance precision, accuracy, and ease of use. NeuroSAPHIREX is capable of...

**PSC I**: - Coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix. - Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system. - Ensures allocated tasks are performed on time, within budget and to a high quality standard. Escalates in...

**Description** **Principal Medical Writer** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our...

India, Remote **Job ID** R0000017927 **Category** Clinical Trials **ABOUT THIS ROLE**: **TMF Support** - Collaborates with the TMF Inspection Readiness Specialist to plan and execute assigned tasks. - Maintains overview of the agreed planning, proactively providing status updates and notifying trends to the study team and TMF IR Specialist. - Stays...

Job Overview Provide project related assistance for assigned project(s), sites and project teams. Lead teams functionally, where assigned, including awareness of scope of work, budget, and resources. Ensure all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements and meets quality...

**Description** **Principal Safety & Pharmacovigilance Specialist** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide...

The Pharmacovigilance Information Specialist (PVIS) for GPIO (Global Pharmacovigilance Information Office) will research, review, and maintain information related to expedited and periodic safety reporting requirements for both clinical trial studies and post market projects. The PVIS works to ensure company and client compliance with relevant national and...

1) Qualification: B.E./B.Tech Computer Science(appearing/completed) or Equivalent/MCS/MCA 2) Knowledge in.Net, C#, C++ and basic SQL 3) Requirements review 4) Coding/Programming 5) Unit Testing Clario is a 50+ year old company that delivers industry leading clinical trial endpoint technology solutions. The future of clinical trials is vibrant, with new...

New England Info Tech LLC, a startup IT Consulting firm with established clients in Biotech and Healthcare, is hiring! This is an opportunity to get your foot in the door of an already profitable, stable, and growing Tech Consulting firm under leadership of a team with 12+ years of experience in the industry. Your work and contributions will have real...

**Description** **Quality Assurance Associate** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our...

Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. **What you will be doing**: Serve as a Clinical Data reviewer and identify any errors in data by...

**Description** **Associate Director, Biostatistics** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to...

TMF SupportCollaborates with the TMF Inspection Readiness Specialist to plan and execute assigned tasks.Maintains overview of the agreed planning, proactively providing status updates and notifying trends to the study team and TMF IR Specialist.Stays flexible and always looks for proactive, responsible solutions to ensure client satisfaction.Provides...

Job Overview Acts as Lead Medical Writer on more advanced writing projects (e.g. complex clinical study reports, protocols, more challenging indications, or customers). Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. May provide feedback to peers when...

Key Responsibilities:Work with the Business Owner to justify the project, agree to scope, define System requirements, assist the business with user acceptance testing, and to ensure acceptance of the final deliverable.Coordinate and provide system and process training for the user group.Lead meetings with stakeholders, SMEs, project managers, and team...