Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Hav[...]
$95k - $210.9kSyneos Health/ inVentiv Health Commercial LLC
Sr. Principal Regulatory Medical Writer - Oncology Preferred Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full‑Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver - for one another, our customers, and, most importantly, for those in need. Job Responsibilities Develop regulatory documents for submission to regulatory agencies globally, including Clinical Study Reports, Clinical Summaries of Efficacy and Safety, and Clinical Overviews, in accordance with ICH and other global guidelines, standards and processes, and Incyte authoring standards, as applicable, in adherence with study/project timelines and corporate objectives. Manage medical writing projects, including developing timelines (working with the study/project teams, as necessary) and communication with cross‑functional team members to maintain awareness of review cycles and expectations. Participate in cross‑functional meetings to provide input regarding medical writing deliverables, timelines, and any process(es) needed for the completion of regulatory documents. Review other documents associated with the assigned project(s) (eg, Protocols and Statistical Analysis Plans), as appropriate. eCTD submission experience preferred. At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality‑of‑life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements. Salary Range: $95,000.00 - $210,900.00 The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. #J-18808-Ljbffr Syneos Health/ inVentiv Health Commercial LLC
$95k - $210.9k
Syneos Health/inVentiv Health Commercial LLC is seeking a Sr. Principal Regulatory Medical Writer in Arizona to develop regulatory documents, manage... ...candidate will have extensive experience in preparing submissions for regulatory agencies globally and will be rewarded...PrincipalSeniorRegulatoryFlexible hours$70.1k - $145k
Job Responsibilities Senior medical writer on clinical study or regulatory project teams. Writes, edits, and coordinates content for clinical/regulatory... ..., safety update reports, development plans, IND/IND submissions, integrated summary reports, NDA and eCTD...SeniorRegulatoryFlexible hours- ...pharmaceutical, biotech, and medical device industries... ...trial data and regulatory submission challenges. With a global... ..., the Medical Writer will critically evaluate... ...bias Write and edit clinical development documents... ...pharmaceutical industry Must have at least 3-5...SeniorRegulatoryRemote jobWorldwide
- ...Sr Medical Writer Publications - Sponsor Dedicated - Remote Based Syneos Health is a leading... ...customer success. We translate unique clinical, medical affairs and commercial... ...scientific meetings. Adheres to established regulatory standards, including, but not limited...SeniorRegulatoryContract workRemote workFlexible hours
- ...quality and excellence.We are Worldwide Clinical Trials, and we are a global team of... ...'ll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for... ...Psychiatry is strongly preferredCandidates must reside on the West CoastWillingness to...SeniorRegulatoryWork at officeRemote workWorldwide
- ...talents to a leader in medical technology and... ...procedures to a wide range of clinical base including... ...Adheres to financial, regulatory, quality compliance standards... ...standards and requirements MUST HAVE - BASIC... ...offered exclusively for Principal-level roles and above,...PrincipalRegulatoryH1bWork at officeLocal areaImmediate startRemote workMonday to FridayFlexible hoursNight shift
- ...Overview We are partnering with a leading organization... ...program to identify a Clinical Quality Reviewer. This... ...will be doing Review medical records to identify potential... ...compliance with regulatory requirements and... ...program integrity What you must have Active, unrestricted...RegulatoryWork at officeRemote workHome office
- ...activities at sites participating in Worldwide’s clinical research projects. Typically involved in... ...with sites to collect appropriate regulatory documents and supporting the negotiation... ...is strongly preferred Candidates must reside on the West Coast Willingness to...SeniorRegulatoryWork at officeRemote workWorldwide
- .... Position Summary The Clinical Study Documentation Specialist... ...operating procedures (SOPs), regulatory requirements, and industry... ...Institutional Review Board (IRB) submissions, engaging with research sites... ...of Employment: Individual must successfully complete pre-employment...RegulatoryWork at officeLocal area
$173.68k - $258.19k
Overview The AD&D Systems Engineer -Advanced FlightControls Sr Principal is a visionary and hands-on engineer responsible for the early... ...environmental, operational, regulatory and service domains. Engineer... ...Health Coverage: Medical, vision, dental, with additional...PrincipalSeniorRegulatoryTemporary workWork at officeFlexible hoursWeekend work- ...Job Purpose The Clinical Research Associate (CRA) has... ...for study start-up and regulatory maintenance. Tasks may... ...application process; submission of proper application/... ...timely feedback to the Principal Investigator,... ...Collaborates with local Medical Science Liaisons (MSLs...SeniorRegulatoryLocal areaRemote workFlexible hoursShift work
- ...leading biopharmaceutical solutions organization is seeking a Sr Medical Writer for remote-based opportunities. The role involves leading... ...sciences, proven experience in medical writing, and strong regulatory knowledge. The position offers valuable benefits including medical...SeniorRegulatoryRemote workFlexible hours
- ...Full‑time Clinical Research, Regulatory Associate Working from our Phoenix, AZ office... ...start‑up activities, IRB submissions, and ongoing electronic... ...equivalent experience supporting medical device regulatory... ...Authorization All candidates must be legally authorized to work...RegulatoryFull timeH1bWork at officeVisa sponsorshipWork visaMonday to FridayFlexible hours
$68k - $71.03k
...Claims Clinical Documentation Reviewer Division of Fee for Service... ...organizations in support of billed medical, behavioral health, NEMT and... ...compliance with contractual, regulatory, and statutory obligations... ...employees are subject to and must successfully complete the...RegulatoryFull timePart timeWork at officeRemote workLong distance$85k - $92k
...Location: Remote Schedule: Must work AZ hours (typically 1st... ...license: RN Minimum 3+ years clinical experience (med/surg and/or... ...THEY ACTUALLY DO) Review medical records for quality, safety,... ...Ensure compliance with regulatory and program standards IDEAL...RegulatoryHourly payRemote workDay shift- Clinical Department Supervisor III Location: Peoria, AZ Overview Lead clinical operations to ensure high-quality patient care, staff performance, and regulatory compliance. Supervise clinical teams, manage workflows... ...with EHR systems Must be 21+; AZ driver’s license...RegulatoryRemote work
- ...uncapped commission plan. Position Overview The Clinical Liaison Support is a... ...based enteral nutrition and medical supply services. This role combines... ...healthcare compliance and regulatory standards Ability and... ...environment Physical Requirements Must be able to speak, read,...RegulatoryWork at officeLocal areaRemote work
$106k - $149k
...Edwards Lifesciences Belgium is seeking a Sr. Specialist in Clinical Science/Medical Writing. This role focuses on supporting regulatory and clinical document development for the Transcatheter Mitral & Tricuspid Therapies team. Key responsibilities include literature...SeniorRegulatoryRemote work- ...Company A well-funded, clinical-stage biotechnology... ...compliance with all regulatory requirements and... ...with clinical leads and medical monitors, serving as the... ...interactions. Applicants must have an M.D. or... ...high-quality, timely submissions to regulatory agencies...SeniorRegulatory
- ...directly supports life-saving medical testing and patient care.... ...established policies, procedures, regulatory and accreditation... .... Requires manual dexterity. Must use standard precautions due... ...Qualifications Previous clinical laboratory experience. Successful...RegulatoryMonday to FridayShift workWeekend work
- ...Participate in mock regulatory examinations and compliance program reviews. Assist with policy and procedure reviews. Draft reports and manuals for compliance. Provide compliance assistance to clients including private funds and registered products. Take a leading role...PrincipalSeniorRegulatory
$183k - $215k
...WestLand! WestLand is seeking a Senior Principal Consultant, Water Resources to join our... ...engineering discipline or in a related field. Must have a P.E. license. Preference will be... .... Expertise in Federal and Local regulatory water/wastewater standards. Ability to foster...PrincipalSeniorRegulatoryFull timeLocal areaRemote workFlexible hours$97k - $193k
Worldwide Clinical Trials, a global CRO, is seeking a Senior Clinical Research Associate (CRA) for remote work in the United States.... ...conducting study initiation visits, and ensuring compliance with regulatory requirements. Qualified candidates will have 5+ years of...SeniorRegulatoryRemote jobWorldwide- ...directly supports life-saving medical testing and patient care.... ...established policies, procedures, regulatory and accreditation... .... Requires manual dexterity. Must use standard precautions due... ...PREFERRED QUALIFICATIONS Previous clinical laboratory experience. Successful...RegulatoryMonday to FridayShift workNight shiftWeekend work
- ...leading biopharmaceutical solutions organization is seeking a Sr Medical Writer for remote-based opportunities. The role involves leading... ...sciences, proven experience in medical writing, and strong regulatory knowledge. The position offers valuable benefits including medical...SeniorRegulatoryRemote jobFlexible hours
- ...looking to hire a full‑time Clinical Research Laboratory... ...Upon Hire Position Overview A DAY IN THE LIFE OF A... ...compliance with quality and regulatory requirements.... ...Laboratory Science, or Medical Technology from an accredited... ...All candidates must be legally authorized...RegulatoryFull timeH1bVisa sponsorshipWork visaMonday to Friday
- Castle Biosciences Inc. is hiring a full‑time Clinical Research, Clinical Safety Manager to lead safety activities for LDT, IVD and medical device studies. The role oversees safety... ...event management, risk assessments, and regulatory documentation to ensure participant...SeniorRegulatoryFull time
- ...Vice President of Clinical Pharmacology About the Company... ...strategic input for NDA/MAA submissions, and contributing to the interpretation... ...pharmacology sections for regulatory submissions, as well as... ...stages. Applicants must have a medical degree or an advanced scientific...Regulatory
- ...2024 Industry Pharma/Biotech/Clinical Research Work Experience 1-3... ...procurement of budgets, contracts, regulatory documents, and other... ...final reports for regulatory submission. Assist with the maintenance... ...successfully, an individual must be able to perform each essential...RegulatoryWork experience placement
- ...execution, dissemination and interpretation of clinical and population health analyses, metrics... ...delivery, provider relationships and regulatory issues Sophisticated knowledge of how... ...confidential customer information that must be protected at all times. In connection...SeniorRegulatoryFor contractorsWork at officeLocal areaShift work
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