Oncology Medical Writer (Remote/Hybrid) - Regulatory & Trials
Voronoi
Voronoi is seeking an experienced Medical Writer with a strong background in oncology clinical trials to join our growing team. The ideal candidate will craft high-quality regulatory and scientific documents and collaborate with cross-functional groups to advance clinical development. This remote or hybrid role requires familiarity with ICH guidelines, regulatory submissions, and effective scientific communication. #J-18808-Ljbffr
Vacancy posted 4 days ago
Similar jobs that could be interesting for youBased on the Oncology Medical Writer (Remote/Hybrid) - Regulatory & Trials in Waltham, MA vacancy
- ...is seeking a Research Nurse to coordinate oncology clinical trials, focusing on multiple myeloma and related... ...research experience and familiarity with regulatory processes, EMR systems, and patient education. Hybrid onsite/remote work may be available. #J-18808-Ljbffr...Remote workRegulatory
UT MD Anderson Cancer Center
Austin, TX1 day ago - ...International, Inc. is seeking a Medical Writer Associate in Bethesda, MD.... ...for clinical trials with hands-on drafting of medical and regulatory documents. The position is full-time, hybrid (2 days at the Bethesda office and 3 days remote), requiring strong written...Remote jobRegulatoryFull timeWork at office3 days per week
- ...Global Laboratories is seeking a Medical Writer to interpret complex... ...clinical studies, ensuring regulatory compliance and high-quality... ...communication. The role is remote (East Coast) with standard hours... ...and experience in clinical trials or lab settings. #J-18808-...Remote workRegulatory
951 ACM Medical Labs, Inc
United States4 days ago - ...SCRI), a McKesson subsidiary, seeks a Medical Writer to research, write, and edit clinical... ...documents across therapeutic areas. This remote role requires coordinating with... ...writing experience in clinical research, oncology trials, and a solid understanding of GCP/ICH...Remote workWork at office
McKesson’s Corporate
Nashville, TN3 days ago - ...study protocols, the full-time Clinical Trials Medical Writer will prepare and coordinate laboratory... ...with internal departments in a remote role based on the East Coast. Key responsibilities... ...in compliance with SOPs and regulatory requirements Author and finalize global...Remote workRegulatoryFull timeWork at office
Virtual Vocations Inc
United States22 hours ago $77k - $92k
...Description Job Title: Medical Writer Department: Study Set Up Location: Remote East Coast | Must Sit in East Coast... ...operating procedures (SOPs) and regulatory requirements. With support of... ...working knowledge of clinical trials. Resolve queries for complex...Remote workRegulatoryWork at officeLocal areaMonday to FridayFlexible hoursRochester Regional Health
Rochester, NY3 days ago- ...programs to advance oncology treatments and... ...the most innovative medical minds together with... ...world. Medical Writer The Medical Writer... .... This is a remote position based in... ...with submissions to regulatory authorities, including... ...oncology clinical trials Thorough understanding...Remote workRegulatoryWork experience placementWork at officeRelocation package
Sarah Cannon
Nashville, TN3 days ago - ...Brigham, seeks a Clinical Research Associate to ensure regulatory requirements for clinical trials are met. You will work with clinical teams, IRBs,... ...regulations governing clinical research. Remote Type Hybrid; Work Location 55 Fruit Street. The role requires a...Remote workRegulatory
1200 The General Hospital Corporation
Boston, MA3 days ago - ...In-House Clinical Research Associate to support a CRO providing clinical trial management and regulatory services. The hybrid role is based in Bethesda, MD, with 2 days onsite and 3 days remote per week. You will review regulatory documents, maintain TMF in electronic...Remote workRegulatory3 days per week
Piper Companies
Bethesda, MD2 days ago - ...monitor, and analyze late‑phase trials in growth hormone and related therapies... ...in the United States, with a hybrid arrangement from the Princeton office, or remote for the right candidate.... ...teams, analyzing data, drafting regulatory submissions, and maintaining up‑...Remote workRegulatoryWork at office
Ascendis Pharma
Princeton, NJ1 day ago - ...lead end-to-end management of Clinical Trial Agreements (CTAs), FMV negotiations,... ...trial sites, ensuring CTAs meet regulatory requirements and that documentation... ...is complete and audit-ready. This hybrid role allows 20%–40% remote work. The position requires 7+ years...Remote workRegulatoryContract work
Genmab A/S
Princeton, NJ1 day ago - ...ALX Oncology is seeking a Clinical Trial Manager / Sr. CTM to drive global oncology trials from protocol through... ...maintaining high quality. Strong regulatory knowledge and TMF stewardship are... ...two days weekly as part of a hybrid model in South San Francisco, CA. Competitively...Regulatory
ALX Oncology
South San Francisco, CA2 days ago - ...Institute in Brookline, MA seeks a Regulatory Coordinator II to manage regulatory... ...research projects under the Clinical Trials Office. You will prepare submissions... ...policies and federal regulations. Hybrid work with 2–3 days remote/onsite; collaboration with OHRS, ODQ...Remote workRegulatoryWork at office
Dana-Farber Cancer Institute
Brookline, MA2 days ago - ...NCRI) in Somerville, MA is seeking a Clinical Trial Assistant Project Manager (Systems use) to... ...staff, manage data and budgets, and ensure regulatory compliance across the Research Portfolio. This role can be hybrid or remote, with on-site duties at 399 Revolution Drive...Remote jobRegulatory
$130k - $189k
...Overview Selective Insurance is seeking a Trial/Sr. Trial Attorney for our Wayne, PA... ...in compliance with applicable legal and regulatory requirements. This is a hybrid role, currently with 2 days in office and 3 days remote, subject to change dependent upon business...Remote workRegulatoryWork at officeLocal areaSelective Insurance Company of America
Wayne, PA3 days ago- ...Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation... ...License Required Hybrid Position RESPONSIBILITIES... ...oral oncology medications, prescription verification... ...accordance with regulatory requirements and... .... Ability to work remotely effectively as...Remote workRegulatoryPrivate practiceMonday to FridayRotating shift
Florida Cancer Specialists
Fort Myers, FL22 hours ago - ...ACM Global Laboratories, Inc. is seeking a Medical Writer to interpret complex clinical study protocols and prepare study-specific medical... ...with multiple departments to ensure accuracy and regulatory compliance. Responsibilities include leading document development...Remote workRegulatory
ACM Global Laboratories
Rochester, NY4 days ago $109.8k - $164.7k
...Managed: Clinical trials in North AmericaOverviewThe... ...(CTLM) is a Hybrid office-based... ...with project plans, regulatory requirements, GCP,... ...through data reviews (remote and onsite)•... ...development experience in oncology.• Extensive... ...contributions up to 6%• Medical, dental, and...Remote workRegulatoryInterim roleWork at officeLocal areaNight shiftWeekend work3 days per weekEUSA Pharma
Bridgewater, NJ22 hours ago- ...AI healthcare company to hire a Medical Writer for the clinical team. The role is remote in the United States and contract... ...Writing, Clinical Science, Regulatory Writing or similar backgrounds with... ...pharma writing are invited to apply. Oncology experience is preferred. #J-18...Remote workRegulatoryPermanent employmentContract work
Elixir Associates LTD
United States3 days ago $138.32k - $163.99k
...four therapeutic areas -Oncology, Inflammation,... ...transforming your career. Local Trial Manager Duties:... ...study reports, regulatory submissions, or other... ...clinical monitoring, and medical affairs; Partner with... ...work models, including remote and hybrid work arrangements,...Remote workRegulatoryFull timeLocal areaFlexible hoursAmgen
Thousand Oaks, CA1 day ago- ...Associate/Monitor to coordinate multicenter investigator-initiated oncology trials within the MGB Cancer Institute Clinical Trials Office. This... ...CRA will oversee site activation, training, monitoring, and regulatory compliance without direct patient contact. Responsibilities...Remote workRegulatoryWork at office
Mass General Brigham
United States22 hours ago $190k - $230k
...Director, Clinical Trial Operations About... ...applicable global regulatory requirements. Responsibilities... ...in cell therapy, oncology, or complex... ...requirements and medical terminology for... ...and able to work a hybrid schedule in the office... ...San Francisco or remote. Embodies the...Remote workRegulatoryContract workWork at officeLocal areaFlexible hoursShift workNkarta Inc
South San Francisco, CA4 days ago- ...The University of Kansas Medical Center Cancer Center is seeking a Regulatory Coordinator to manage study-specific regulatory and safety reporting across multiple clinical trials. You will ensure compliance with CFR, GCP, HIPAA and organizational policies. Responsibilities...Remote workRegulatory
University of Kansas Medical Center
United States3 days ago - ...The Clinical Trial Manager (CTM) is responsible... ..., applicable regulatory requirements, ICH-... ...This role can be hybrid to Norwood, Ma onsite... ...3 days a week or remote with monthly... ...Management, Statistics, Medical and other... ..., experience with oncology is preferred Site...Remote workRegulatoryContract work3 days per week
Corbus Pharmaceuticals
Norwood, MA22 hours ago $128k - $160k
...Principal Medical Writer, Regulatory & Scientific Writing Location: Remote or Hybrid in San Diego Employment Type: Full time Reports To: President & Founder About Aroga... ...and effectively present scientific and clinical trial data, with a strong understanding of statistical...Remote workRegulatoryFull timeAroga Biosciences
United States4 days ago- ...include patient recruitment, data collection, and ensuring regulatory compliance across IRB and GCP standards. The CRN role offers hybrid work after an initial training period, with proximity to the Massey Clinical Trials Office and disease-working group teams. #J-18808-...RegulatoryWork at office
Commonwealth of VA Careers
Virginia, MN3 days ago - ...Proclinical seeks a GCP QA Consultant to support oncology-focused clinical programs in a fully remote US-based role. You will ensure compliance... ...quality improvements, and prepare for regulatory inspections across global trials. Responsibilities include reviewing trial...Remote workRegulatory
ProClinical
United States4 days ago - ...Senior CTM with vendor management experience to oversee complex multi-country oncology trials. You will manage study timelines, budgets, contracts, and sites across regions, ensuring regulatory compliance and high-quality data. Strong leadership and collaboration with...Remote workRegulatoryWork from home
Syneos Health Inc
United States2 days ago - ...Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to oversee clinical... ...focuses on quality, patient safety and regulatory compliance, acting as a partner to sites... ...years as a regional traveling CRA with Oncology trial monitoring experience, and the...Remote workRegulatoryWork from homeWorldwide
Worldwide Clinical Trials
United States4 days ago $109k - $174.8k
...Information Job Function: Medical Affairs Group Job Sub... ...best talent for a Medical Writer III, Regulatory Medical Writing to... ...Switzerland. The position is Hybrid (3 days onsite weekly). Remote work options may be considered... ...Regulations, Clinical Trials Operations, Coaching,...Remote workRegulatoryLocal areaJohnson & Johnson Innovative Medicine
Raritan, NJ2 days ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Oncology Medical Writer (Remote/Hybrid) - Regulatory & Trials. Be the first to apply!
Related searches
- medical customer service representative Waltham, MA
- medical and health service manager Waltham, MA
- medical driver Waltham, MA
- non emergency medical transportation Waltham, MA
- medical director global medical affairs Waltham, MA
- medical delivery driver Waltham, MA
- medical solutions Waltham, MA
- medical clerical Waltham, MA
- director medical information Waltham, MA
- medical office part time Waltham, MA