Emmes Group Jobs in India

The Ophthalmic Certification Project Associate (OCPA) is critical to the successful conduct of ophthalmic certifications in Biopharmaceutical-sponsored clinical trials. · ...

Emmes Group is transforming the future of clinical research bringing the promise of new medical discovery closer within reach for patients. · ...

The Therapeutic Area Safety Manager will manage all activities of all Safety Monitors assigned within the Therapeutic Area. · ...

We believe in the power of truth, so much so that we named our company Emmes, which means truth. Through decades of experience we have learned that collaborative relationships thrive and human health benefits when truth is our compass. · ...

We believe the work we do will have a direct impact on patients' lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. · We're looking for talented professionals eager to help advance clinical r ...

We believe the work we do will have a direct impact on patients' lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. · We're looking for talented professionals eager to help advance clinical r ...

This job involves designing, developing and enhancing cloud-based SaaS web-based clinical trials applications. · Responsibilities include collaborating with product, engineering and software quality assurance team members for integration, design and verification in an agile envir ...

We are seeking an experienced Sr. Data Scientist to join our team in Bengaluru. As a key member of our data science team, you will be responsible for developing and deploying AI/ML models that drive innovation and efficiency. · Develop scalable and high-performance ML models usin ...

+ · Job summary · The Safety Monitor will implement Pharmacovigilance activities in collaboration with other members of the Pharmacovigilance and Medical Monitoring (PMM) department. · +Assists in performing safety monitoring activities in cooperation with project Medical Monitor ...

+The Director of Biostatistics & Statistical Programming will have several years of leadership level experience in managing people and projects, interacting with clients, and work experience as a Biostatistician developing protocols, writing statistical analysis plans, performing ...

We are looking for a talented professional to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us. · The Manager, OptymEdge Enterprise Operations executes enterprise-level ...

The Safety Monitor I will implement Pharmacovigilance activities in collaboration with other members of the Pharmacovigilance and Medical Monitoring (PMM) department, under direct supervision. · ...

OptymEdge · a Veridix company within the Emmes Group, · is transforming ophthalmology clinical development by digitizing manual processes and data collection into streamlined workflows. · The Director, Product Management OptymEdge will define and drive the strategy,vision,and exe ...

The Senior Procurement Specialist is dedicated to managing sourcing and procurement of specialized clinical trial materials and equipment. · ...

We believe the work we do will have a direct impact on patients' lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. · ...

++Assists in performing safety monitoring activities in cooperation with project Medical Monitor/Medical Officer and other relevant project team members+ · Reviews safety events+ · +Assists in the collection, assessment, monitoring, review and reporting of adverse drug reaction c ...

OptymEdge a Veridix company within the Emmes Group is transforming ophthalmology clinical development by digitizing manual processes and data collection into streamlined workflows. · ...

We believe the work we do will have a direct impact on patients' lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We're looking for talented professionals eager to help advance clinical res ...

The TMF Manager/Senior Manager is responsible for leading and managing the Trial Master File operations team to ensure high-quality, compliant, and efficient delivery of TMF services across clinical projects.The role provides operational oversight, supervises TMF staff, ensures a ...

We're looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. · Designs, develops, and enhances cloud-based, SaaS web-based clinical trials applications. · Collaborates with product, engineering, an ...