Remote Senior Medical Writing Lead for Clinical Submissions
Latigo Bio
- Remote job
Latigo Bio is seeking an experienced Associate Director of Medical Writing to lead authoring and management of pivotal clinical and regulatory documents, focusing on protocols, amendments, and CSRs for a growing portfolio. The role partners with Clinical Development, Regulatory Affairs, Statistics, and others to ensure timely, compliant, and scientifically rigorous submissions. Travel may be required for team meetings and deadlines. #J-18808-Ljbffr Latigo Bio
$150k - $195k
...Therapeutics is looking for an Associate Director, Medical Writing, responsible for leading regulatory submissions and ensuring high-quality documentation.... ...collaboration with cross-functional teams and entails remote work with some onsite presence in San Diego. #J-...Remote workSeniorMedical- ...seeking an Associate Director-Medical Writer to lead and drive the development... ...scientific documents for submissions and internal communications. You will coordinate with clinical development, regulatory, biostatistics... ...8+ years in medical writing within pharma/biotech/CRO,...SeniorMedical
- ...Lifesciences is seeking a Senior Specialist, Medical Writing to act as the primary contact... ...projects within the Clinical Affairs team. You will collaborate... ...writing deliverables, lead negotiations on timelines,... ..., and support regulatory submissions (US/EU/international) with...SeniorMedical
- Veristat, a global clinical research company, is seeking a Senior Medical Writer with a clinical focus to lead document authorship across service... ...expertise in regulatory writing to support Clinical Study... ...successful health authority submissions while collaborating #J-18...Remote jobSeniorMedical
- SimulStat Inc. seeks a Sr. Medical Writer to support the development of global regulatory... ...for reviewer-friendly clinical documents to support regulatory agency... ...requires a strong background in medical writing, regulatory submissions, and project management, with 6-8...Remote jobSeniorMedical
- ...Senior Clinical Scientist This position reports to Manager/Sr. Manager, Medical Sciences and requires a strong candidate with expertise... ...requirements in support of submission for CE Mark application to obtain... ...scientific literature and write clinical summaries for...Remote workSeniorMedical
- ..., MA, is seeking a Principal Medical Writer (equivalent to Associate Director) to lead medical writing on multi-disciplinary teams and... ...contract writers on the clinical program. You will develop key... ...ensure timely, high-quality submissions. #J-18808-Ljbffr Alnylam PharmaceuticalsSeniorMedicalContract work
- ...Holdings Inc in Boston is seeking a Medical Writer to evaluate medical literature and prepare clinical documents, including clinical... ...least 3-5 years of regulatory writing experience in the... ...members and ensuring high-quality submissions to regulatory authorities. #J...Remote jobSeniorMedical
- A leading staffing firm is seeking a Medical Author to document clinical data and regulatory submissions to support drug development. This role requires expertise in analytical writing, project management, and collaboration with product teams to ensure high-quality deliverables...SeniorMedical
- ...Inc is seeking a skilled Medical Writer in Chicago. The successful... ...background in regulatory writing, including clinical protocols and study... ...scientific field and experience in leading teams. This role is vital... ...research and regulatory submissions. #J-18808-Ljbffr MMS...Remote jobSeniorMedical
- ...an experiencedClinical Regulatory Writing Associate Director to lead regulatory writing across a complex... ...You will author the most intricate clinical-regulatory documents and ensure regulatory... .... The role requires leading submission strategies (cSCS), mentoring teams,...Senior
- MMS Holdings Inc in Baltimore, Maryland is seeking a Medical Writer to critically evaluate and write clinical documents for regulatory submissions. This role demands experience in the pharmaceutical industry and exceptional writing skills to produce high-quality documentation...Remote jobSeniorMedical
$270k - $360k
...Medical Director/Senior Medical Director, Clinical DevelopmentTenvie Therapeutics is developing... ...Director to lead early- and mid-... ...support regulatory submissions partnering closely... ...This role can be remote, hybrid, or on-site... ...scientific and medical writing skills; able to...Remote workSeniorMedicalLocal area- ...seeking a Manager, Regulatory Medical Writing to support across key therapeutic... ...country postings and potential remote options. You will lead preparation of clinical documents, guide cross-... ...ensure regulatory compliance across submissions. Strong leadership, writing, and...Remote workMedical
- Arvinas is a clinical-stage biotechnology company... ...an experienced Senior Medical Director with the... ...in and lead an innovative drug... ...with a hybrid or remote work arrangement... ...preparation and submission of IND, CTA, and... ...in the planning, writing, and review of Clinical...Remote workSeniorMedicalContract workLocal areaHome office
- Atorus seeks a senior statistical lead to support an active regulatory submissions program, focusing on statistical review, submission... ..., Regulatory Affairs, Medical Writing, and external partners to... ...submission-ready deliverables. Remote work from anywhere in the U.S...Remote workSeniorMedicalFull time
$125k - $180k
...Clinical Development Scientist/Senior Clinical Development Scientist... ...This role can be remote, hybrid, or on-site... ...prioritization Lead or co‑lead the... ...Participate in ongoing medical and scientific... ...in regulatory submissions (e.g., IND/CTA,... ...scientific writing skills with a track...Remote workSeniorMedicalInterim roleLocal area- ...Clinical Research AssociateFor the past 25 years, ProPharma... ..., pharmacovigilance, medical information, and R&D... ...both in person, and remote. This includes... ...for monitoring report writing and completion within... ...documents, Ethics Committee submissions, and other site set up...Remote workSeniorMedicalInterim roleWork at officeLocal area
$325k - $358k
...of Alumis as a senior leader and spokesperson for Clinical Development within... ...psoriasis, leading one or more studies... ..., Biomarkers, Medical Affairs,... ...generation, as well as submission activities... ...medical monitoring, writing papers)... ...Thursday. Open to remote applicants with...Remote workSeniorMedical$268k - $302k
...Senior Director, Clinical PharmacologyCambridge, MA - RemoteAmylyx... ...support regulatory submissions and successful drug... ...Medicine, Nonclinical, Medical Writing, and external... ...will independently lead assigned programs while... ...we proudly support remote work opportunities within...Remote workSeniorMedicalLocal area- Natera is looking for a Senior Clinical Scientist to lead clinical development for their early cancer detection program. This role involves overseeing... ...science. Competitive benefits include comprehensive medical plans and generous leave policies. #J-18808-Ljbffr NateraRemote jobSeniorMedical
$247.65k - $298.8k
...Therapeutics is a late-stage clinical biopharmaceutical... ...will successfully lead and/or serve as... ...Development, Medical Affairs,... ...with registration submission strategies and can... ...contributor to the writing of protocols/major... ...Proven ability to work remotely and with remote internal...Remote workSeniorMedicalFlexible hours- ImmunityBio, Inc. is seeking a Senior GCP Auditor to ensure GCP compliance across its trial operations. The role collaborates with Clinical Operations, Regulatory, Pharmacovigilance, Medical Writing, and Data Management to maintain readiness and uphold quality standards...Remote jobSeniorMedical
- ProPharma in Raleigh, NC seeks an experienced Medical Writer to lead clinical and regulatory documents across drug, biologic, and device programs. You will author, edit, and supervise deliverables, mentor junior writers, and ensure compliance with ICH E3/E6, FDA rules,...Remote jobSeniorMedical
- A leading global clinical research organization is seeking a Senior Medical Writer I for a 12-month FTC, fully remote. In this role, you will spearhead the development and execution of medical writing initiatives supporting innovative therapies. The ideal candidate will...Remote jobSeniorMedicalFixed term contract
$137.2k - $205.8k
...Pharmaceuticals in Boston is looking for a Medical Writing Science Senior Manager to independently author complex clinical study documents. This hybrid role allows for remote work two days a week, ensuring flexibility while leading critical regulatory writing activities....Remote workSeniorMedical2 days per week- Veristat is seeking a Principal Medical Writer to independently plan and prepare regulatory... ...candidates have 7+ years in regulatory writing, a Bachelor's degree with MS or PhD preferred, and strong leadership to guide submission-level documents and #J-18808-Ljbffr VeristatRemote jobSeniorMedical
- ...leadership and provide senior-level addiction... ...support to clinic partners, and support... ..., risk reduction, medication treatment for opioid... ...approaches. Contribute to writing study... ...participants and teams remotely; therefore, access... ...Research Area Specialist Lead level, applicants...Remote workSeniorMedicalContract workTraineeshipWork at officeFlexible hoursWeekend workAfternoon shift
$125k - $180k
...Clinical Scientist/Senior Clinical Scientist Tenvie Therapeutics... ...This role can be remote, hybrid, or on-... ...: Lead development of core... ...training material, medical monitoring plans,... ...involvement in regulatory submissions (e.g., IND/CTA,... ...scientific writing skills with a track...Remote workSeniorMedicalFull timeLocal area- ...Pharmaceuticals Incorporated is seeking a Medical Writing Science Senior Manager to author complex clinical study documents and sections of regulatory submissions to support all phases of clinical... ...position is hybrid, with 2 days remote per week and 3 days in the Boston...Remote workSeniorMedicalWork at officeFlexible hours2 days per week
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Remote Senior Medical Writing Lead for Clinical Submissions. Be the first to apply!
- junior remote developer Thousand Oaks, CA
- remote senior salesforce administrator Thousand Oaks, CA
- remote entry level web developer Thousand Oaks, CA
- remote travel jobs Thousand Oaks, CA
- remote no experience Thousand Oaks, CA
- remote medical billing part time Thousand Oaks, CA
- entry level front end developer remote Thousand Oaks, CA
- data science internship remote Thousand Oaks, CA
- remote data entry part time Thousand Oaks, CA
- senior accountant remote Thousand Oaks, CA


