Lead Medical Writing Scientist, Clinical & Regulatory
Scorpion Therapeutics
Scorpion Therapeutics in Boston, Massachusetts seeks a Medical Writing Science Manager to prepare clinical and regulatory documents. This role involves authoring, reviewing, and ensuring consistency in documentation while collaborating with cross-functional teams. The ideal candidate holds a Ph.D. with at least 4 years of relevant experience. Strong communication and project management skills are essential. This position offers an opportunity to impact the drug development process through effective document management. #J-18808-Ljbffr Scorpion Therapeutics
$150k - $200k
Medical Writing Lead, Global Clinical Operations, Orion Pharma Cambridge, United Kingdom and 3 more (Hybrid) Job Description Orion Pharma is a purpose... ...across all phases of drug development and global regulatory submissions, ensuring quality and compliance through leadership...RegulatoryWorldwide- Merida Biosciences is seeking a Director, Medical Writing to lead development of clinical and regulatory documents supporting our advancing pipeline in a fast-paced biotech environment. Reporting to the Senior Director, Regulatory Affairs & Medical Writing, you will author...Regulatory
- ...Responsibilities Provide strategic medical guidance for... ...for Translational Clinical Oncology (TCO) aspects... ...subsequent registration trials. Lead Biomedical Research... ...experts, investigators, and regulatory authorities; act as... ...for global studies; write/review abstracts/manuscripts...RegulatoryWorldwide
$39 - $48.02 per hour
Clinical Laboratory Team Leader - Blood Bank Location: Boston, MA... ...Available About the Opportunity A leading healthcare organization is... ...established procedures and regulatory requirements. Evaluate specimen... ...Clinical Laboratory Science, Medical Technology, Biology,...RegulatoryHourly payTemporary workBank staffLocal areaRelocation packageMonday to FridayShift work$29.01 per hour
...protocols, this role provides assistance on clinical research studies, including recruiting,... ...visits and procedures. Assists with regulatory binders and QA/QC procedures. Assists with... ...as literature review and scientific writing, and with operational tasks such as managing...RegulatoryHourly payDaily paidRemote workShift work- ...Overview The Director Clinical Scientist is an important and... ...with the Clinical operations lead and medical director. The Director Clinical... ...or reviews safety or regulatory documents and updates them... ...~ Demonstrated scientific writing skills ~ Embraces Artificial...Regulatory
$168k - $188k
...close out of domestic and international clinical studies, including study concept and... ...clinical trial‑related trackers such as regulatory documents, trial master file (TMF), startup... ...Assurance, Data Management, Biostats, Medical Writing, Safety, Clinical Supply, Finance)...RegulatoryContract workLocal areaRemote work- ...pioneering sleep technology company based in Boston is looking for a Senior Clinical Trials Manager to oversee the execution of clinical studies and manage regulatory trials. This role involves writing IRB submissions, overseeing third-party clinical sites, and ensuring...Regulatory
- ...revolutionary discoveries in medical innovations in... ...seeks to hire a full-time Clinical Research Coordinator I... ...and submission of regulatory documents (e.g., IRB submissions... ...possess: Excellent writing skills and experience... ...ideas, we choose to lead. All qualified...RegulatoryFull timeTraineeshipWork experience placementWork at officeRemote workShift work
$21 - $29.01 per hour
...applications for 1 full‑time Clinical Research Coordinator (CRC) to... ...clinically severe psychiatric and/or medically acute patients and strong... ...are strongly preferred. Writing, computer skills (e.g., proficiency... ...for study visits; ensuring regulatory compliance; and maintaining...RegulatoryHourly payDaily paidFull timeWork experience placementRemote workShift work$112.5k - $165k
...of the studySet up and lead the study Cross... ...collaboration with the Medical Asset Lead, SP and MSL... ...partnership with the Global Regulatory team to ensure... ...the CSR with Medical Writing.Ensure the finalization... ...Deep knowledge of Good Clinical Practice (GCP) for CPMs...RegulatoryTemporary workWork at officeLocal areaFlexible hours- ...Clinical Trial Manager PROMETRIKA is a full-service clinical... ...management, biostatistics, medical writing, and pharmacovigilance. We're... ...compliant with SOPs, ICH/GCP/regulatory guidelines, study protocol,... ...managing timelines and budgets, leading risk assessments, and...RegulatoryContract workWork experience placement
- ...Lahey Health's Cardiovascular MRI Research Center seeks a Senior Clinical Research Coordinator to support investigator-initiated and NIH... ...MRI studies, coordinating multi-site teams and ensuring regulatory compliance. You will recruit participants, obtain consent, manage...Regulatory
- Medium in Cambridge, Massachusetts is seeking a Senior Clinical Trial Manager to lead daily activities in clinical trials, ensuring compliance and... ...teams and external vendors to meet compliance with regulatory standards. Qualifications include a Bachelor's or Master'...Regulatory
- ...Position: Clinical Research Nurse II, Cancer Location: Boston, MA... ...per week ABOUT BMC At Boston Medical Center (BMC), our diverse staff... ...perspective and information to regulatory coordinators as needed to... ...Previous experience with grant writing, IRB submissions, data management...RegulatoryLocal area
- Seaport Therapeutics is a clinical-stage biopharmaceutical company... ...extensive network of renowned scientists, clinicians and key opinion leaders... ...(CTM) is responsible for leading the execution of clinical... ...leadership for the development and writing of study protocols, study...3 days per week
- Simcere Zaiming in Cambridge, Massachusetts is seeking a Clinical Trial Manager to oversee and manage clinical trials. The role involves ensuring compliance with regulatory requirements and company policies while coordinating with cross-functional teams. The candidate should...Regulatory
$75k - $105k
Regional Travel, Clinical Research Coordinator Quincy, Massachusetts... ...need, and contribute to the medical breakthroughs of tomorrow. How... ...provided timelines Assist regulatory personnel with completion and... ...Communicate clearly verbally and in writing Anticipate needs; propose...RegulatoryBi-weekly payFull timeTemporary workWork at officeLocal areaVisa sponsorshipWork visaFlexible hours- ...Therapeutics, based in Boston, is looking for a Clinical Trial Leader (CTL) to oversee cross-functional clinical... ...strong interpersonal skills, the ability to lead diverse teams, and a detailed understanding of regulatory compliance, along with experience in global clinical...Regulatory
- AstraZeneca is seeking a Clinical Study Administrator to assist in coordinating clinical study activities from start-up to execution... ...team members to deliver support while ensuring compliance with regulatory requirements. The ideal candidate will have a Bachelor's Degree...RegulatoryLocal area
$150k - $200k
A biopharmaceutical company is seeking a Medical Writing Lead to oversee the creation of clinical documents across drug development stages. The successful candidate... ...of medical writing experience and expertise in regulatory submissions. This hybrid role allows employees to...Regulatory$232k - $401.35k
...Function: Discovery & Pre-Clinical/Clinical Development... ...and execution of medical and scientific strategies... ...Clinical Team (CT). The CL leads the team to develop... ...documents for global regulatory filings. The CL will... ...data management, medical writing, biostatistics, global...RegulatoryFull timeLocal areaImmediate start$220k - $260k
Verastem Oncology in Boston is seeking an experienced medical writer to produce high-quality clinical documentation. The ideal candidate will possess strong expertise in clinical and regulatory writing and utilize AI tools effectively to enhance document quality and efficiency...Regulatory- ...International GmbH is seeking a senior leader in Clinical Pharmacology to drive strategy from first‑... ..., and safety data across programs and lead MIDD initiatives in collaboration with pharmacometrics, statistics, and regulatory teams. The role requires mentoring junior staff...Regulatory
- A leading biotech company based in Boston is looking for a Director, Clinical Operations Program Lead to oversee the execution of global oncology clinical studies. This... ...vendor oversight, and ensure compliance with regulatory standards. Competitive compensation is...Regulatory
- ...seeking a seasoned biostatistician to serve as the statistical lead for one or more clinical programs in the U.S. You will provide technical... ...with cross-functional teams to shape development plans and regulatory interactions. You will oversee the statistics and programming...Regulatory
- ...Clinical Data Management Lead Lead and manage clinical data management activities for oncology clinical trials, ensuring adherence to project... ...data validation plans in alignment with study protocols and regulatory requirements. Oversee the design, build, and...Regulatory
- Scorpion Therapeutics is seeking a Clinical Data Manager based in Boston, Massachusetts. The role involves overseeing clinical data management... ..., including vendor management and ensuring compliance with regulatory standards. The ideal candidate will possess over 8 years of...Regulatory
- ...re looking for a Growth Lead, Partnerships &... ...prospective partners: audience, clinical credibility, market... ...Nothing publishes without medical sign‑off Manage... ...community, and outreach. You write within the brand voice... ...preferred. You understand the regulatory environment, patient...RegulatoryFixed term contract
$248.5k
...Provides strategic medical guidance and leads the development of experimental... ...at PE / DCC. Create clinical development... ...with clinical scientists to develop clinical... ...investigators, and regulatory authorities in oncology... ...groups and authorities. Write and review abstracts...RegulatoryWork at officeLocal areaWorldwide
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