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Contractor - Director, GDS&PV Medical Writer
System One
Job Title: Contractor - Director, GDS&PV Medical Writer
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Lead Clinical Dietitian
The Children's Hospital of Philadelphia
Plans and initiates medical nutrition therapy for patients if indicated by patient requirements and clinical protocol including but not limited to complex enteral nutrition regimens and…
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Lead Clinical Dietitian
The Children's Hospital of Philadelphia
Plans and initiates medical nutrition therapy for patients if indicated by patient requirements and clinical protocol including but not limited to complex enteral nutrition regimens and…
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Clinical Protocol Writer
Actalent
Job Title: Clinical Protocol Writer (REMOTE) WITH ONCOLOGY ACADEMIC INSTITUTIONDuration: 6-12 Month renewable contract ****20 hours per week for the first few months then could increase to…
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Clinical Protocol Writer (ONCOLOGY)
Actalent
***MUST HAVE EXPERIENCE WRITING ONCOLOGY PROTOCOLS AT AN ACADEMIC INSTITUTION/CANCER CENTER!!
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Clinical Protocol Writer (ONCOLOGY)
Actalent
***MUST HAVE EXPERIENCE WRITING ONCOLOGY PROTOCOLS AT AN ACADEMIC INSTITUTION/CANCER CENTER!!
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Associate Director, Medical Writing
Lexicon Pharmaceuticals is currently recruiting for a collaborative, agile, results focused Senior Medical Writer to join our team in either in Bridgewater, New Jersey, The Woodlands,…
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Technical Writer III
Fisher Clinical Services, Inc.
Must possess the ability to define problems, collect data, establish facts, and draw valid conclusions · Must have the ability to effectively present information and respond to questions from senior management, peers, and clients
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Clinical Protocol Writer (ONCOLOGY)
Actalent
***MUST HAVE EXPERIENCE WRITING ONCOLOGY PROTOCOLS AT AN ACADEMIC INSTITUTION/CANCER CENTER!!
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Director/Sr. Director, Discoverability
Immortals
Brief and manage all specialist contractors and vendors: technical SEO engineer, content writer, transcript pipeline engineer, schema vendor, LLM tracking vendor, Wikipedia consultancy, PR…
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Quality Control Specialist, Medical Writing
BeOne Medicines
Experience in conducting medical writing QC reviews of pharmaceutical industry regulatory documents (such as clinical study reports, protocols, and protocol amendments) or experience in…
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Senior Director Clinical Development – Early Development Team Leader (EDTL)
Mitsubishi Tanabe Pharma America
study protocols and clinical development plans. The role will include oversight
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Medical Writer I, II or III
Mitsubishi Tanabe Pharma America
As a key member of our Clinical Development Team, the Medical Writer will provide regulatory documents support to the clinical teams, ensuring successful preparation of high quality,…
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Scientific Writer II / III, Preclinical Research
Pharmaron
Position: Scientific Writer II / III, Preclinical Research
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Contract Medical Writer
Evolution Research Group
The Contract Medical Writer assists in managing various aspects of medical writing activities, ensuring efficiency and compliance with regulations. This role encompasses responsibilities…
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Sponsor Dedicated Senior Medical Writer (Regulatory Submission Documents)- US Remote Based
Syneos Health, LLC
This Sponsor dedicated role will involve partnering closely with Clinical Scientist and will be focused on Protocols and Protocol Amendments.
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Medical Writer - Perlmutter Cancer Center Clinical Trials Office
NYU Langone Medical Center
To qualify you must have a Bachelors degree preferably in science, public health, health education or a related field
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Director, Global Medical Writing
Deciphera Pharmaceuticals
…Director, Global Medical Writing. The individual will be the lead writer across programs/submissions that are part of the growing clinical…
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Clinical Study Physician - Oncology - FSP
Parexel International, LLC
Responsible for medical content of Clinical Trial Protocols (CTPs), in line with TDO, in collaboration with the Clinical Trial Lead (CTL), Clinical Program Lead (CPL), Patient Safety…
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Medical Operations Leader
Parexel
The Senior Clinical Scientist (SCS) may lead or support a study or studies, depending on size/complexity. The SCS as lead is accountable for the clinical/scientific execution of the…
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Clinical Development Medical, Associate Director
Pfizer Inc
Contributes towards the medical input during protocol development and updates to the clinical development plan.
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Senior Clinical Scientist - Oncology - Home Based
ICR United States USA
If no degree in Life Sciences, must have significant experience in clinical development (>11 years)
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Senior Editor-Medical Oncology
The Ohio State University
Minimum of 4 years of relevant scientific or medical writing and editing experience required
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Clinical Trials Medical Writer
RochesterRegional Health
Description Job Title: Medical Writer Department: Study Set Up Location: Remote East Coast | Must Sit in East Coast Hours Per Week: 40 hours Schedule: Days, Monday - Friday SUMMARY The…
