Clinical Trials Medical Writer

Everest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in...

Job SummaryWe are seeking a detail-oriented and organized Clinical Research Coordinator II to join our team. In this role, you will be responsible for coordinating and managing multiple clinical trials simultaneously, ensuring timely and accurate completion of tasks and responsibilities.Main ResponsibilitiesClinical Trial Coordination: Oversee the daily...

About UsPharma Medica Research Inc. is a leading provider of clinical trial services. Our team of experts conducts early phase clinical trials in healthy volunteers and special patient populations.We're seeking a highly skilled Medical Recruiter to join our team.

Job Description:Innovative Medicine at Johnson & Johnson is a hub for groundbreaking advancements in healthcare solutions. We foster an environment where science meets patients' needs, driving the development of tomorrow's treatments.We are seeking a seasoned Medical Writer Lead to join our team in North America, Europe, or other global locations. As a key...

Job OverviewJohnson & Johnson is a leading healthcare company that aims to prevent, treat, and cure complex diseases. We are looking for an experienced Oncology Medical Writer Lead to join our team in developing innovative treatments and medicines.This role will involve writing and coordinating clinical and regulatory documents, as well as leading...

Company OverviewPharma Medica Research Inc. is a leading contract research organization specializing in early phase clinical trials.We are committed to delivering exceptional results and strive for excellence in all aspects of our work.We currently have an exciting opportunity for a Medical Recruiter to join our team.

About the PositionThis position offers the opportunity to work on high-profile clinical trials and develop expertise in clinical development. The Senior Clinical Research Director will lead cross-functional teams to achieve clinical trial goals and objectives.Key ResponsibilitiesDevelop and implement clinical development strategies for assigned program...

Clinical Trial AssociateThe Clinical Trial Associate will be responsible for setting up, tracking and maintaining Clinical Site related documents. You will help manage and review regulatory documents as well as maintain the Local Study File. Assist with coordinating the distribution, retrieval and review of regulatory documents required for the initiation of...

We are seeking a motivated and experienced Senior Medical Writer to join our team in Toronto/Markham, Ontario, Canada. The ideal candidate will have an advanced degree, preferably a Ph.D., in Clinical or Medical or Life Sciences, or a Master's degree with substantial experience in the subject matter.About the Job DescriptionIn this role, you will receive...

Role OverviewThe GCP Compliance Manager, Program is a key role within the organization responsible for ensuring the compliance of regulated activities across clinical trials. This position requires a strong understanding of regulatory requirements, excellent organizational and analytical skills, and a proven track record of delivering high-quality results in...

Job SummaryThe Senior Global Clinical Trial Assistant will be responsible for overseeing the setup, tracking, and maintenance of clinical site-related documents. This role requires strong organizational skills to manage and review regulatory documents as well as maintain the Local Study File.This position is part of a dynamic team at ICON Strategic Solutions...

Ecrscorp is a leading contract research organization providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.About UsWe have a...

Job OverviewPharma Medica Research Inc. is a full-service contract research organization specializing in conducting early-phase clinical trials in healthy volunteers, special, and patient populations. Our team is dedicated to delivering high-quality research services and seeking talented individuals to join our growing organization.

About the RoleWe are seeking a skilled Clinical Research Coordinator to join our team at the Rotman Research Institute. In this role, you will be responsible for coordinating and supervising all study activities, ensuring proper execution of assigned clinical research trials, and meeting regulatory requirements.The ideal candidate will have a strong...

Job DescriptionThis Clinical Trial Governance Lead role is responsible for driving the adoption of Risk-based Quality Management (RBQM) practice at trial level, overseeing implementation, and continuous improvement.Main Accountabilities:Risk Assessment and Mitigation: Facilitate trial protocol risk assessment across multiple cross-functional domains...

Job OverviewWe are looking for a highly skilled Risk Management Lead for Clinical Trials to join our team. As a key member of our organization, you will be responsible for driving the adoption of Risk-based Quality Management (RBQM) practices at trial level, overseeing implementation, and ensuring continuous improvement.The ideal candidate will have a strong...

Medical Oncology Practice OpportunityJoin Northeastern Ontario's healthcare leaderHealth Sciences North (HSN) is recruiting health care professionals who have a keen interest in affecting change within its dynamic health care system. As the tertiary care referral centre for the entire Northeastern Ontario region, HSN serves a catchment population of over...

Required Skills and QualificationsTo succeed in this challenging role, you will need to possess a strong background in clinical research, with at least 10 years of experience in global drug development spanning phases I through IV. Your expertise should encompass all aspects of conducting clinical trials, including planning, execution, reporting, and...

Ecrscorp is committed to delivering high-quality clinical research services to our clients. As a Senior Medical Writer, you will play a critical role in achieving this goal by developing comprehensive clinical study reports and other regulatory documents.About the RoleThis is an exciting opportunity to work on challenging projects and contribute to the...

Job Description SummaryIn close collaboration with the Global Program Safety Lead (GPSL), provides robust safety evaluation expertise and medical innovation to improve patients' lives and impact on overall Novartis results. As a member of the Medical Safety organization, prioritizes the safety of patients, ensures optimal patient safety for assigned...