icf

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...

Job OverviewUnder moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements  at the regional, or country level. Prepares and manages site documentation; reviews and negotiates site  documents and contracts with sites and sponsors;...

Career CategoryRegulatoryJob DescriptionJob SummaryClinical trial activities are growing rapidly and dynamically, and we are currently seeking a full-time, Clinical Trials Regulatory Submissions Manager to join our Local Regulatory in Amgen Korea. This position plays a key role in the clinical trial application management, import licenses and regulatory...

Job OverviewUnder moderate supervision, executes the feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level.Prepares and manages site documentation; reviews and negotiates site documents and contracts with sites and sponsors;...

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...

Job OverviewUnder moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements  at the regional, or country level. Prepares and manages site documentation; reviews and negotiates site  documents and contracts with sites and sponsors;...

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...

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...

Precision for Medicine is a Clinical Research Organization. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in...

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...

우리 회사를 한 줄로 표현해주세요 우리 회사에 대해 4줄 이내로 소개해주세요 임상관련 17개 포지션 모집부문 및 자격요건 모집부문 담당업무 자격요건 인원 임상 [담당업무] 문의 사항 있으시면 언제든지 연락 주시기 바랍니다. 1. 임상기획운영(차~부장급) / 중견제약회사...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5...

**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...

Job DescriptionPurpose of the JobTo lead Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with AZ Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations.In addition to leading LST(s), the Local Study...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the...

**Job Description** **Purpose of the Job** - To lead Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with AZ Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations. - In addition to leading LST(s), the...

**Job Description** **Purpose of the Job** - To lead Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with AZ Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations. - In addition to leading LST(s), the...

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 (CA) and/ or...