Hackensack Meridian Health Inc.
Medical Writer Clinical Trials
Hackensack Meridian Health Inc., Hackensack, New Jersey, us, 07601
Our team members are the heart of what makes us better.
At
Hackensack Meridian Health
we help our patients live better, healthier lives — and we help one another to succeed. With a culture rooted in connection and collaboration, our employees are team members. Here, competitive benefits are just the beginning. It’s also about how we support one another and how we show up for our community.
Together, we keep getting better - advancing our mission to transform healthcare and serve as a leader of positive change.
The
Medical Writer Clinical Trials
is responsible for analyzing, writing and editing technical documentation summarizing clinical study ideas into protocols and resulting publications as well as writing summarizing other scientific matters. This role will contribute to developing and implementing comprehensive workflows and project planning to ensure ongoing clinical trial compliance across the Disease Specific Oncology Research Programs. This includes, but is not limited to, overseeing and driving the clinical research trials development and analysis process to final deliverables in a timely and effective manner. This role will collaborate and communicate with teams of investigators and research staff to ensure continual process development and improvement, always emphasizing clarity in training and implementation with the highest standards of integrity.
Education, Knowledge, Skills and Abilities Required
Bachelor's degree in a scientific or medical discipline.
Minimum of 5 or more years of experience in clinical healthcare environment.
Solid knowledge of Good Clinical Practice guidelines and Protection of Human Subjects regulations.
Strong attention to detail and customer service focus is required.
Excellent medical writing, communication, organizational, presentation, documentation, and interpersonal skills.
Ability to work independently, or in a team, and handle multiple deadline driven tasks in a dynamic environment is essential.
Review and comply with all relevant HMH and Business Unit policies and procedures, and local, state, and Federal laws and regulations.
Mandatory education on human subject research and GCP (CITI Training and Certification).
Possesses beginning to working knowledge of subject matter.
Excellent written and verbal communication skills.
Proficient computer skills that include but are not limited to Microsoft Office and/or Google Suite platforms.
Education, Knowledge, Skills and Abilities Preferred
Higher Education Degree (M.S., PhD, MD).
Knowledge of clinical trials and the regulation (local, state, and federal) of such.
Familiarity with basic scientific and healthcare principles and terminology.
If you feel that the above description speaks directly to your strengths and capabilities, then please apply today!
#J-18808-Ljbffr
At
Hackensack Meridian Health
we help our patients live better, healthier lives — and we help one another to succeed. With a culture rooted in connection and collaboration, our employees are team members. Here, competitive benefits are just the beginning. It’s also about how we support one another and how we show up for our community.
Together, we keep getting better - advancing our mission to transform healthcare and serve as a leader of positive change.
The
Medical Writer Clinical Trials
is responsible for analyzing, writing and editing technical documentation summarizing clinical study ideas into protocols and resulting publications as well as writing summarizing other scientific matters. This role will contribute to developing and implementing comprehensive workflows and project planning to ensure ongoing clinical trial compliance across the Disease Specific Oncology Research Programs. This includes, but is not limited to, overseeing and driving the clinical research trials development and analysis process to final deliverables in a timely and effective manner. This role will collaborate and communicate with teams of investigators and research staff to ensure continual process development and improvement, always emphasizing clarity in training and implementation with the highest standards of integrity.
Education, Knowledge, Skills and Abilities Required
Bachelor's degree in a scientific or medical discipline.
Minimum of 5 or more years of experience in clinical healthcare environment.
Solid knowledge of Good Clinical Practice guidelines and Protection of Human Subjects regulations.
Strong attention to detail and customer service focus is required.
Excellent medical writing, communication, organizational, presentation, documentation, and interpersonal skills.
Ability to work independently, or in a team, and handle multiple deadline driven tasks in a dynamic environment is essential.
Review and comply with all relevant HMH and Business Unit policies and procedures, and local, state, and Federal laws and regulations.
Mandatory education on human subject research and GCP (CITI Training and Certification).
Possesses beginning to working knowledge of subject matter.
Excellent written and verbal communication skills.
Proficient computer skills that include but are not limited to Microsoft Office and/or Google Suite platforms.
Education, Knowledge, Skills and Abilities Preferred
Higher Education Degree (M.S., PhD, MD).
Knowledge of clinical trials and the regulation (local, state, and federal) of such.
Familiarity with basic scientific and healthcare principles and terminology.
If you feel that the above description speaks directly to your strengths and capabilities, then please apply today!
#J-18808-Ljbffr