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
$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$70 - $80 per hour
...$70.00/hr - $80.00/hr Sr. Medical Writer Job Summary: Talent Software... ...and reporting the results of clinical studies, including protocols... ...used in the preparation of regulatory filings (eg, briefing books,... ...Integrated Summary of Safety (ISS), Integrated Summary of...SeniorRegulatoryPermanent employmentFull timeContract workFor contractorsWork at officeRemote workShift work- ...The Senior Clinical Trial Manager plays a critical role in the strategic planning and... ...within budget, and in compliance with regulatory requirements, GCP guidelines, and internal... ...configuration (CTMS, IRT), regulatory submissions, and operational documentation. Collaborate...SeniorRegulatory
- ...position reports to Manger/Sr. Manager, Medical Sciences and requires a strong... ...literature, data from clinical trials and pre-clinical studies... ...requirements in support of submission for CE Mark application to... ..., product development, regulatory, post‑market surveillance)...SeniorRegulatoryLocal areaWorldwide
$72k - $90k
...patient lives. Whether you’re in clinic operations, product, or... ...of contact for sponsors, IRB submissions, and research participants. Location... ...and organize study files, regulatory binders, and essential... ...and qualifications) Benefits: Medical, dental, vision, PTO, and additional...SeniorRegulatoryFull timeWork at office$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - Southern... ...development. The Sr. Clinical Research Associate... ...Ethics Committee (EC) submissions and confirm approvals.... ...and the client's regulatory inspections. Contribute... ...status. If, because of a medical condition or...SeniorRegulatoryWork experience placementInterim roleLocal areaRemote workFlexible hours- ...A renowned clinical research organization in California is looking for a Clinical Research Associate to oversee monitoring activities... ...monitoring visits, preparing monitoring reports according to regulatory standards, and ensuring data integrity throughout the trial process...SeniorRegulatoryLocal areaRemote work
$70k
...Position Overview We are seeking a highly motivated... ...Senior Entry Writer to join our... ...timely preparation and submission of customs entries... ...company policies and regulatory requirements.... ...communication skills; must be able to... ...health insurance (medical, dental and vision...SeniorRegulatoryWork at officeLocal areaRemote workMonday to FridayAfternoon shift$109.5k - $153.3k
...investigator site facing role, the Sr. CRA will act as a customer... ...goals. Organize and maintain clinical study documentation (e.g.,... ...according to the applicable regulatory requirements. Where appropriate... ...institution, nursing, medical or laboratory technology preferred...SeniorRegulatoryFor contractorsLocal areaRemote work$148.55k - $174.77k
...Company Overview Embark on an enriching journey with... ...? Join us as a Senior Regulatory Affairs Specialist and... ...regulatory science for medical robotics. Your mission... ...submitting regulatory submissions in the US, EU and outside... ...on project teams Must be able to manage multiple...SeniorRegulatory$229k - $240k
...Salary: $229,000 - $240,000 Overview The Director, Clinical Operations will lead and... ...research budget negotiation, medical writing, pharmacovigilance... ..., Project Management, Regulatory Affairs, and Biostatistics... ...scientific congresses, etc. Must adhere to Iovance...RegulatoryContract workWork at officeImmediate startRemote workFlexible hours- ...Company Overview Established in Taiwan in 1974, Hon Hai... ...enterprises. Job Summary The Sr. Business Development... ...sectors, including Medical Electronics and Advanced... .... The ideal candidate must possess a deep professional... ...partnership building. Regulatory & Compliance Oversight:...SeniorRegulatoryContract workLocal areaImmediate start
- ...Role Overview Independently or under... ...supervision of the Regulatory Affairs... ...Assistant Director of Clinical Research... ...Ensuring all submissions and reportable... ...information and assist Principal Investigators... ...individual must accurately... ...located at the UCI Medical Center in...RegulatoryWork experience placementWork at officeLocal area
$30k
...Overview NOTE: This recruitment was amended on April... ...departments into a regular Clinical Laboratory Scientist I... ...position in San Mateo Medical Center (SMMC) may be... ...compliance with regulatory/accreditation agencies... ...biology courses, which must include genetics and immunology...RegulatoryHourly payPart timeWork experience placementImmediate startRelocation packageShift workNight shift- ...Role Senior Manager/ AD, Regulatory Strategy Location Bay Area (Hybrid) About the Organization... ...Our client is a well‑funded, pre‑IPO clinical‑stage biotechnology company focused on... ...play a key role in preparing for BLA submission. Key Responsibilities Lead global regulatory...SeniorRegulatoryRemote work
$71k - $166k
## Dialysis Clinical Manager Registered Nurse... ...Manager with Fresenius Medical Care, you will... ..., compliance and regulatory requirements and programs... ...kidney disease. PRINCIPAL DUTIES AND... ...and the employee must be able to bend over... ...$166,000 Benefit Overview: This position offers...RegulatoryTemporary workWork experience placementWork at office- ...Description The Clinical Trials Manager (CTM) supports the conduct of clinical trials and... ...biotechnology industry Knowledge and Skills Must have a demonstrated track record of... ...knowledge of FDA, ICH, GCP, CFR guidelines, regulatory requirements and clinical trial...RegulatoryWork at officeLocal areaRemote work
$71.9k - $189k
...Clinical Research Associate, Sponsor Dedicated California, United... ...eligible for this position, you must reside in the same country... ...studies by tracking regulatory submissions and approvals, recruitment and... ...commercialization of innovative medical treatments to help improve patient...RegulatoryFull timePart timeLocal areaImmediate startWorldwide$90k - $130k
..., TN, TX, WA Vanguard Clinical, Inc. is a Contract Research... ...for pharmaceutical, medical device and... ...the results. Position Overview Reporting to the Director... ...external commitments. Must exercise sound judgment... ...ICH/GCPs and applicable regulatory requirements. Solid computer...RegulatoryPermanent employmentFull timeContract workInterim roleWork at officeRemote workFlexible hours$90k - $105k
...Overview Join our Supply Chain team as the Sr. Supply Chain Analyst at Endologix! WHO WE ARE:... ...California-based global medical device company dedicated... ...therapeutic portfolio addresses clinically relevant unmet needs,... ...company standards and regulatory expectations. Support...SeniorRegulatoryFor contractorsWork at officeLocal areaRemote workWork from homeFlexible hours$75.7k - $90k
...address inadequate medical care in the region... .... Job Summary The Clinical Research Program... ...with the Director, Principal Investigators (PI)... ...daily administrative, regulatory, financial, and... ..., writing, and submission to federal agencies... ...representative of those that must be met by an...RegulatoryFull timeContract workWork at officeLocal area$136k - $192.5k
...Summary The Clinical Trials Manager (CTM), Clinical Operations, coordinates... ...relevant departments (e.g., Regulatory Affairs, Drug Safety,... ....g., SAB, BOD, DT, TAT, DSC, DOC) Support or be responsible for... ...understand technical, scientific, and medical information Demonstrated...RegulatoryContract workLocal areaFlexible hours- ...Serve as the study biostatistician for assigned clinical oncology studies, contributing to the development and execution of statistical... ...and data analysis issues related to clinical trials and regulatory submissions. Author and contribute to key statistical documents and...SeniorRegulatoryWork at officeWeekend workAfternoon shift
- ...Stanford Health Care job. A Brief Overview Performs a wide range of medical laboratory tests used to diagnose,... ...Senior, Reference, or Supervising Clinical Laboratory Scientist. Calibrates assays... ...safety/health and state/federal regulatory requirements and the procedures,...RegulatoryFull timeWork experience placementNight shift
- ...Overview Family Health Services Clinics of the Health and Social Services Department (FHS) is currently recruiting... ...‑quality, comprehensive, accessible medical and dental care to support Solano... ...are encouraged to apply. Applicants must meet the stated qualifications above...SeniorAfternoon shift
- ...Job Title Clinical Research Coordinator Reports to CRC Manager Job... ...nurses. Liaise with regulatory and quality assurance departments... ...documents. Assist with study submissions. Report protocol deviations... ...and enroll subjects. Collect medical history. Conduct study visits...RegulatoryMonday to Friday
$105k - $120k
...Quidel Corporation and Ortho Clinical Diagnostics, creating a... ...future for all. The Role Senior Regulatory Affairs Specialist. This role... ...in vitro diagnostics and medical devices worldwide. Responsibilities... ...U.S. and IVDR regulatory submissions, interacting with regulatory...SeniorRegulatoryWork experience placementWork at officeRemote workWorldwideHome officeNight shift- ...Type: Direct hire LMFT Required Overview A behavioral health... ...area is seeking an experienced Clinical Supervisor to join their clinical... ...documentation meets quality, regulatory, and funding requirements Support... ...and/or participation in medical, dental, and vision benefits...RegulatoryInternshipWork at officeLocal areaRemote work
$93.6k - $114.4k
...Clinical Trial Assistant W2 Contract-to-Hire Salary Range: $93,600 - $114,400 per year Location... ...development and maintenance of RCR (Regulatory Compliance Review) packs for Phase I... ...Additionally, candidates for this position must qualify as a W2 candidate. Bayside...RegulatoryContract work- ...that address high unmet medical needs. About The Role... ...Director/VP of Regulatory Affairs reports to the... ...regulations, standards, and clinical practice guidelines. This... ...Requests, IND submissions, Annual Reports, ensure... ...labeling is required. Must be capable of developing...RegulatoryLocal areaFlexible hoursShift work
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