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DescriptionYou 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 30-minute video sessions on our platform.This is a freelance remote role with the flexibility to decide your business...

Are you a Counselor, Psychologist, or Coach looking to work remotely and provide quality mental health support to clients? MindFi, a Mental Health and Wellbeing platform, is looking for Care Providers to join our network. As a Care Provider, you will play an integral role in making high-quality care accessible to people across Asia-Pacific Region and...

DescriptionThe Regulatory Start-Up Associate (RSA) and Regulatory Start-Up Lead (RSL) are responsible for the planning, preparation, and review of country- and site-level ethics and regulatory authority submissions during the start-up phase of clinical trials, and, where applicable, throughout maintenance and close-out. They ensure that all submissions...

Essential Functions Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager(SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), WorkPerform feasibility, site ID, start up and site activation activities...

Location: minimum ​2 ​days ​onsite in ​Waltham, MA office Cambridge / ​Greater ​BostonVoronoi is ​seeking a dynamic ​Medical Director ​who ​thrives in ​a ​fast-paced ​environment to partner ​cross ​functionally with drug ​discovery, ​translational ​medicine, clinical operations, ​clinical investigators ​and...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure...

Job Description SummaryThis role involves managing translation and copy-editing tasks, ensuring high-quality linguistic deliverables for assigned projects or accounts. Responsibilities include coordinating with freelancers and agencies, maintaining language resources, resolving terminology queries, and collaborating with clients and internal teams to enhance...

Job Description Summary This role involves managing translation and copy-editing tasks, ensuring high-quality linguistic deliverables for assigned projects or accounts. Responsibilities include coordinating with freelancers and agencies, maintaining language resources, resolving terminology queries, and collaborating with clients and internal teams to...

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure...

Who we areWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.We are Worldwide Clinical Trials, and we are a global...

Job Overview:Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites, this role ensures smooth progression from feasibility and initial outreach...

You will be responsible for:Quality and timeliness of  study deliverables (site identification, feasibility, start up, recruitment, data deliverables, filing of complete study documentation) for assigned study(ies).Proactive reporting of study-specific issues (including monitoring metrics) to the global study team and country leadership teamQuality of...

What You'll Do Assist/Advise project teams on all regulatory requirements for clinical studies  Perform compliance assessments according to country requirements and document any activity discovered; notify Project Managers of any findings  Review and adapt study specific documents according each country and site requirements   Perform...

About usBeOne is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse pipeline of novel therapeutics through our internal capabilities and collaborations. We are committed to radically...

About PROTEINA프로티나의 ​핵심 ​경쟁력은 ​자체 개발한 ​SPID(Single-molecule Protein-protein InteractionDetection) 기술입니다. ​SPID는 ​생명현상의 기본 ​단위인 단백질 간 ​상호작용(Protein-ProteinInteraction, PPI)을 ​기존 ​기술로는 구현하기 ​어려웠던 ​정확도와 ​민감도,...

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 30-minute video sessions on our platform. This is a freelance remote role with the flexibility to decide your business hours....

You Will Be Responsible For Quality and timeliness of study deliverables (site identification, feasibility, start up, recruitment, data deliverables, filing of complete study documentation) for assigned study(ies). Proactive reporting of study-specific issues (including monitoring metrics) to the global study team and country leadership team Quality of...

**What You'll Do** - Assist/Advise project teams on all regulatory requirements for clinical studies - Perform compliance assessments according to country requirements and document any activity discovered; notify Project Managers of any findings - Review and adapt study specific documents according each country and site requirements - Perform IRB/EC...

The Regulatory Start-Up Associate (RSA) and Regulatory Start-Up Lead (RSL) are responsible for the planning, preparation, and review of country- and site-level ethics and regulatory authority submissions during the start-up phase of clinical trials, and, where applicable, throughout maintenance and close-out. They ensure that all submissions comply with...