Mentors and leads less experienced medical writers on complex projects, as necessary. Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. We translate unique clinical, medical affairs a...
The Senior Medical Writer reports to a Director of Medical Writing. The Senior Medical Writer is expected to develop and maintain a network of internal relationships with global and local cross-functional study teams, including personnel from Medical & Science, Clinical Pharmacology, Biostatisti...
THE COMPANY Octane Learning is a professional learning and medical communications agency, working exclusively for pharmaceutical, biotech, medical device, and healthcare companies. THE WORK Reporting to the Director of Content and Strategy, you’ll develop the content for: (1) several dif...
Responsibilities: Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias Write and edit clinical development d...
Create and/or co-create and review medical content for patients, HCPs and payers to ensure scientific rigor, balance and impact, this includes field medical slides (Medical Science Liaisons and Managed Care Liaisons), and standard or complex medical information responses. As needed, provide medical ...
The Senior Medical Writer reports to a Director of Medical Writing. The Senior Medical Writer is expected to develop and maintain a network of internal relationships with global and local cross-functional study teams, including personnel from Medical & Science, Clinical Pharmacology, Biostatisti...
Essential Functions Authors, edits, and provides QC review of documents to support clinical trials and regulatory submissions, which may include: Clinical study protocols and protocol amendments Clinical study reports (CSR) Investigator brochures (IB) Informed consent and assent forms Lay summaries ...
You're an established Senior Medical Writer looking for the next challenge, or an experienced Medical Writer aiming to move up. Senior Medical Writers define new directions with CMC Affinity. IPG Health Medical Communications is home to the world’s most celebrated and awarded med comms agencies, uni...
The Senior Medical Writer reports to a Director of Medical Writing. The Senior Medical Writer is expected to develop and maintain a network of internal relationships with global and local cross-functional study teams, including personnel from Medical & Science, Clinical Pharmacology, Biostatistics, ...
Build strong relationships with Creative, Medical, Account, and Client brand teams, such that each group identifies you as the holder of all copy, editorial and clinical knowledge for the brand. Partner with Creative, Medical/Strategy, Account and Client teams to ensure copy that advances creative b...
Essential Functions+ Authors, edits, and provides QC review of documents to support clinical trials and regulatory submissions, which may include:+ Clinical study protocols and protocol amendments+ Clinical study reports (CSR)+ Investigator brochures (IB)+ Informed consent and assent forms+ Lay summ...
THE COMPANY Octane Learning is a professional learning and medical communications agency, working exclusively for pharmaceutical, biotech, medical device, and healthcare companies. THE WORK Reporting to the Director of Content and Strategy, you’ll develop the content for: (1) several dif...
As part of our expanding US Medical Affairs (USMA) team, Genmab is seeking a Senior Director, USMA Solid Tumor Portfolio. Serve as a medical and content expert for internal and external stakeholders, representing Genmab at key Global and US medical conferences, at US advisory boards and at internal ...
As Medical Director at Genmab, you will be accountable for the medical oversight of one or more clinical trials, medical review and communication of data, and medical input into regulatory documents, and presentations. The Role & Department Genmab continues to grow and is currently seeking a Medical...
Our client is seeking to add its first Technical Writer to their department and is seeking a candidate who brings a knack for creativity, who is passionate for building structure out of ambiguity, who will proactively pursue informational details where needed, and is comfortable speaking face-to-fac...
Job Title: Senior Medical Editor. Maintaining and distributing Client- /product-specific guidelines among staff editors. Serving as the Client’s contact authority for all editorial issues. Attendance at all daily status, kick-off, and any other team meetings requiring editorial perspective/input for...
The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports. In parallel, the technical writer could help support non regulatory writing projects such as SOP and technical doc...
The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports. In parallel, the technical writer could help support non regulatory writing projects such as SOP and technical doc...
The CClient Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports. In parallel, the technical writer could help support non regulatory writing projects such as SOP and technical...
This role will develop and lead all medical affairs activities ensuring partnership within the team (medical strategy, scientific communications and publications) all key Medical Affairs functions (Medical Excellence, HEOR, Field Medical, Medical Information) as well as maintaining a high-level cros...
Interested in growing your career? Look no further! TeamHealth is looking for an exceptional OB/GYN physician committed to delivering compassionate high-quality patient care to lead our team at Penn Medicine Princeton Medical Center. Princeton Medical Center is affiliated with the University of Penn...
Responsibilities:Oversee clinical program including component studiesOversee safety of the drug, including the safety aspects of patients in clinical studies and signal detection with support of the Safety physicianLead and oversee creation of clinical components of key documents (regulatory documen...
MARKETING ASSOCIATE/PROPOSAL WRITER - HACKENSACK, NJ. Marketing Associate/Proposal Writer – 0-5+ Years Experience. Marketing Associate/Proposal Writer. Track requests for proposals (RFPs) and ensure that all proposals are submitted on time. ...
Our Global Fortune 500 client is looking for a Technical Writer with the following skills and qualification:. Good experience in writing manuals, technical documentation, job aids, SOPS as well as SDLC documentation. Experience preferred in writing documentation, user guides, technical job aids, PPT...
Copywriter and Digital Marketing Associate Full-time HYBRID (Mon & Thurs in office, adding Tuesday in October) Location: Whippany, NJ Salary: $60,000-63,0000 + Benefits Summary: Jewish Federation of Greater MetroWest NJ is seeking a versatile Copywriter to assist the mar...