Junior Clinical Trials Assistant

Company Description Ergomed PLC is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America, and Asia. Our company allows for employee visibility...

Working under the general direction of the Principal Investigator and as part of the Clinical Research Team, the Clinical Research Assistant supports the Clinical Trials Coordinators in implementing study procedures for assigned research projects. The studies are in the area of Dermatology and include industry-sponsored clinical trials (Phase II-IV) with a...

**HOW MIGHT YOU DEFY IMAGINATION?** You’ve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge you’ve worked hard to acquire and the passion you already have. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology...

**About Our Company**: At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, daring thinking, and innovation - ultimately providing employees with the opportunity to work across teams, functions and even the globe. Recognizing the importance of individualized flexibility, our ways of working allow employees...

Pharma Medica Research Inc. is a Contract Research Organization dedicated to delivering high-quality research services in a highly regulated industry.We are currently seeking an experienced Senior Project Coordinator to join our team. The ideal candidate will have strong organizational and communication skills, with the ability to work effectively in a...

**About Evinova** The Digital Health R&D Recruitment team enables better patient and healthcare professional experiences by delivering customer-centric digital solutions for clinical trials and real-world healthcare. The focus of this role is to work with platform owners, global study teams, and TAs, plus vendors to drive an enterprise-level contact center...

Job SummaryWe are seeking a highly skilled Software Developer - Clinical Trials Analytics to join our team at Pharma Medica Research Inc.About UsPharma Medica Research Inc. is a Contract Research Organization that strives for innovation and original solutions in a highly regulated and competitive industry. We specialize in conducting early phase clinical...

p>The Global Study Associate Director (GSAD) is a business-critical role whose main accountability is the delivery of clinical studies. You will lead a cross-functional study team and provide them with direction and guidance to enable successful study delivery. You are also accountable to the Global Project Team (GPT) for the delivery of a study according to...

Intern, Health Claims and Clinical Trials **Responsibilities**: - Review, evaluate and summarize various studies on food products, nutraceuticals, functional foods, etc. This requires reviewing and interpreting a wide array of studies. In addition to reviewing and interpreting this information, it is required that a critical analysis of this information be...

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the...

Job SummaryWe are seeking an experienced Regulatory Document Specialist to join our team at GlaxoSmithKline. The successful candidate will be responsible for drafting, reviewing, and approving written assignments, including marketing application submission documents.About the RoleThis is a unique opportunity to work with a talented team of experts in...

Job DescriptionWe are seeking an experienced Regulatory Medical Writer to join our team at GSK.The ideal candidate will have a strong background in clinical trial design, research data analysis, and regulatory document writing.About the RoleThis is a senior-level position that requires advanced expertise in clinical document writing, including protocols,...

_**INSTRUCTION TO APPLY; PLEASE APPLY ACCORDINGLY OR YOUR APPLICATION WILL NOT BE ACCEPTED**:_ Cliantha is currently seeking **Part Time Clinical Assistant(s)**; who can fulfill its business needs and is looking for better learning and growth opportunities. **About Us** Cliantha Research is a full service Clinical Research Organization (CRO) that provides...

About UsPharma Medica Research Inc. is a pioneering Contract Research Organization that sets the standard for innovation and excellence in a highly regulated industry.Job SummaryWe are seeking an experienced Senior Data Analyst to join our team of professionals who share a passion for delivering high-quality results.Responsibilities:Create SAS programs for...

At AstraZeneca when we see an opportunity for change, we seize it and commit real resources to make it happen, because an opportunity no matter how small can be the start of something big. Delivering life-changing medicine is about being entrepreneurial - finding those moments and recognizing their potential. Big success can come from seeing potential in...

We are seeking an exceptional Medical Writing Specialist to join our team at Pharma Medica Research Inc. in Mississauga.Company OverviewPharma Medica Research Inc. is a Contract Research Organization that strives for innovation and original solutions in the highly regulated pharmaceutical industry. We specialize in conducting early phase clinical trials in...

Do you have expertise in, and passion for clinical drug development? Are you looking to transform the way cancer is treated and truly improve patient outcomes? Driven by our curiosity, passion and determination we are paving the way to change the practice of medicine in Oncology! AstraZeneca’s Oncology Research and Development teams push the boundaries of...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office Summarized Purpose: Accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time period specified in the contract with the customer. Interprets data on project issues and makes good business...

Job description **Job Description / Roles and Responsibilities for Job Title**: **1) **Assist Associate Director in supervising workload, productivity and work quality of staff, ensuring assigned tasks are completed accurately and within defined performance expectations. Other duties include, but are not limited to: **i. **Supervise performance and...

**ABOUT THE ROLE**: CLINICAL RESEARCH PROGRAM MANAGER, PSS Division, under the direction of the National Lead, Clinical and Outcome Research Operations, and in collaboration with Pharmaceutical companies, Clinical Research Organizations (CROs), health research institutions, or clinical research sponsors, is accountable for the successful implementation of...