Senior Associate, Clinical Trial Submission Management

The Senior Associate, Clinical Trial Submission Management, will help ensure the technical compliance of our Clinical Trial submissions via the smooth compliant flow of information between all functional areas, internal and external to GRAAS, local offices, external partners and regulatory authorities. This vital role is assigned to one or more Amgen...

Job Title: Associate - Clinical Trial Submission Management Job Location: Hyderabad, Telangana, India Job Location Type: On-site Job Contract Type: Full-time Job Seniority Level: What You Will DoLet's do this. Let's change the world. In this vital role you will help ensure technical compliance of our Clinical Trial submissions via the smooth compliant...

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the...

The Senior Associate, Global Submission Management - International, will help ensure the smooth compliant flow of information between all functional areas, internal and external to GRAAS, including local offices, external partners and regulatory authorities within the international (ex-US and Canada) context. This role leads the creation of regulatory...

The Senior Associate, Global Submission Management - Americas, will help ensure the smooth compliant flow of information between all functional areas, internal and external to GRAAS, including local offices, external partners and regulatory authorities within the North American context. This role leads the creation of regulatory submissions through detailed...

Job Title: Clinical Trials Disclosure Associate Job Location: Hyderabad, Telangana, India Job Location Type: On-site Job Contract Type: Full-time Job Seniority Level: Clinical Transparency & Disclosure AssociateRole Name: Clinical Transparency & Disclosure Sr. AssociateDepartment Name: Global Regulatory Affairs & Strategy (GRAAS)Role GCF: 3Hiring Manager...

**Clinical Transparency & Disclosure Associate****Role Name:** Clinical Transparency & Disclosure Sr. Associate**Department Name:** Global Regulatory Affairs & Strategy (GRAAS)**Role GCF:** 3**Hiring Manager Name:** Jennifer Vande Weghe**ABOUT AMGEN**Amgen harnesses the best of biology and technology to fight the world's toughest diseases, and make...

Role OverviewBristol Myers Squibb is an integrated global hub focused on helping patients overcome serious diseases by developing sustainable and innovative solutions. Our technology and drug development activities aim to usher in the next wave of innovation.The Clinical Trial Specialist role has task-level responsibility for document and CTA package...

Job DescriptionWe are seeking a skilled Clinical Trials Specialist to join our team at Bristol Myers Squibb. This individual contributor role has task-level responsibility for clinical trial related document collection, compilation, review and approval across all phases of global clinical trials.Key Responsibilities:Managing and executing on centralized...

**ABOUT AMGEN**Amgen harnesses the best of biology and technology to fight the world's toughest diseases, and make people's lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge...

Let's do this. Let's change the world. In this vital role you will help ensure the smooth compliant flow of information between all functional areas, internal and external to GRAAS, including local offices, external partners and regulatory authorities within the International (non-Americas) context. This role leads the creation of regulatory submissions...

Let's do this. Let's change the world. In this vital role you will help ensure the smooth compliant flow of information between all functional areas, internal and external to GRAAS, including local offices, external partners and regulatory authorities within the North American context. This role leads the creation of regulatory submissions through detailed...

About Bristol Myers SquibbBristol Myers Squibb is a global leader in the pharmaceutical industry, dedicated to developing innovative treatments and therapies for patients around the world. Our company has a rich history of pioneering new medical breakthroughs and advancing the boundaries of human knowledge.Our TeamOur team of experts is passionate about...

We are looking for a seasoned Clinical Trials Leader to join our Bristol Myers Squibb team. As a key member of the Early Clinical Development (ECD) team, you will be responsible for leading the planning and execution of clinical trial activities to support our Clinical Development Plan.About the RoleManage and supervise a team of Clinical Scientists in ECD...

Position Summary / Objective : Manage a team that Reconciles and Prepare Clinical Trial Submission documents adhering to regulatory guidelines and ensuring consistency across all BMS programs Position Responsibilities: - Supervisory responsibility for Clinical Trial Support Specialists, providing support of the in house and outsourced studies in support of...

Transforming patients' lives through science is at the heart of everything we do at Bristol Myers Squibb. As a leader in biostatistics, you will play a critical role in driving innovation and excellence in our clinical trials.Key ResponsibilitiesDesign and analyze clinical trials, including the selection of study population and endpoints to address study...

Manage a team that Reconciles and Prepare Clinical Trial Submission documents adhering to regulatory guidelines and ensuring consistency across all BMS programs- Supervisory responsibility for Clinical Trial Support Specialists, providing support of the in house and outsourced studies in support of CTMS activities to ensure consistency across the team.-...

Position Summary:- Leads the ECD Clinical Science team in the planning and execution of clinical trial activities to support the Clinical Development Plan for the disease/indication team- Responsible for design and execution of assigned clinical trial activities and works closely with clinical team members to execute activities associated with trial...

BMS Hyderabad is an integrated global hub where our work is focused on helping patients prevail over serious diseases by building sustainable and innovative solutions. This important science, technology, and innovation center will support a range of technology and drug development activities that will help us usher in the next wave of innovation. Position...

SUMMARYImaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the Cure. Everything we do is aligned with this singular purpose. We work every day excited to advance imaging science, technology, and services to bring curative technologies to humankind....