89 trial manager jobs at 46 companies in West Warwick, RI
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Clinical Trial Manager
Waltham, Massachusetts, United States
$127k-$155k/yrHybridFull Time
Kailera Therapeutics: Developing clinical-stage injectable and oral therapies for obesity.
6+ YOE6+ years clinical trial experience, strong GCP knowledge, CRO/vendor management, Microsoft Office and Project proficiency, strong communication and analytical skills.
C4 TherapeuticsNasdaq: CCCC: Develops targeted protein degradation therapies to treat cancer diseases.
5+ YOEBachelor’s degree in health, life sciences, or related field and 5+ years of progressive clinical operations experience, including trial management and CRO/vendor oversight.
RFP, FDA Regulations, ICH/GCP, SOPs, IRBs, IND, CTAs
Stoke TherapeuticsNASDAQ: STOK: Develops RNA-based therapies for severe genetic disorders.
8+ YOEBachelor’s degree or higher preferred; 8+ years leading global pivotal clinical trials, with CRO/vendor oversight, ICH-GCP knowledge, clinical operations expertise, project management, and strong communication skills.
Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft PowerPoint, Microsoft Project
Treeline Biosciences: Develops precision medicines for cancer and serious diseases.
5+ YOEBachelor's in biomedical/life science,5+ years clinical trial management experience in Pharma/Biotech/CRO with oncology,experience managing CROs,knowledge of ICH/GCP and global regulations,strong communication and risk management skills.
Xenon PharmaceuticalsNASDAQ: XENE: Developing therapeutics for neurological and psychiatric disorders.
5+ YOEMinimum 5-8 years clinical project/study management experience; bachelor’s degree in a scientific field; strong vendor management and cross-functional collaboration.
Lumicell: Real-time fluorescence imaging for guided cancer surgery.
Bachelor's degree in life sciences, nursing, public health, or related field; clinical trial operations experience; ICH-GCP and FDA knowledge; study start-up, site activation, contracting, and IRB experience.
TScan TherapeuticsNasdaq: TCRX: Developing T-cell receptor-based therapies for cancer and autoimmune diseases.
8+ YOEBachelor's preferred with 8–10+ years clinical research experience, oncology/cell therapy experience preferred, experience leading Phase I–III trials, knowledge of FDA and ICH-GCP, strong communication and organizational skills.
Deciphera Pharmaceuticals: Developing targeted kinase inhibitors for the treatment of cancer.
3+ YOEBachelor's or Master's degree and at least 3 years clinical operations experience in pharma or CRO; solid understanding of ICH/GCP and regulatory requirements; ability to manage trial components independently with strong attention to detail.
Aura BiosciencesNASDAQ: AURA: Developing precision therapies to treat solid tumors.
7+ YOEBachelor's degree and 7+ years of clinical research experience, including 4–5 years in TMF or clinical records management. Requires eTMF experience, ICH-GCP knowledge, analytical skills, and Microsoft Office proficiency.
Veeva Vault, Montrium, Phlexglobal, Ennov, Microsoft Office, Microsoft Excel, Microsoft PowerPoint, CTMS, eTMF, EDC
Dyne TherapeuticsNASDAQ: DYN: Developing therapeutics for genetically driven neuromuscular diseases.
3+ YOE3+ years clinical operations experience, knowledge of ICH-GCP and TMF, bachelor\u0002s degree preferred, strong organization, communication, and ability to manage competing priorities.
eClinical Solutions: Clinical data cloud platform and biometrics services for researchers.
2+ YOEProject management experience (2+ years preferred), professional services delivery, scope and financial management, clinical trial/EDC knowledge preferred, bachelor's or equivalent preferred, Microsoft Suite proficiency, interest in PMP.
Director of the Mandell Trial Advocacy Center, School of Law
Bristol, Rhode Island, United States
OnsiteFull Time
Roger Williams University: Private university offering undergraduate, graduate, and legal degrees.
Lead and manage a multi-semester trial advocacy program, oversee staff and programs, integrate coursework with simulations and competitions, and engage legal practitioners.
Manager or Senior Manager, Patient Recruitment and Retention
Watertown, Massachusetts, United States
$115k-$215k/yrOnsiteFull Time
Kymera TherapeuticsNASDAQ: KYMR: Develops targeted protein degradation medicines to treat human diseases.
5+ YOEBachelor’s degree in a relevant field and 5+ years in patient recruitment and retention, preferably biotech, pharmaceutical, or CRO. Requires clinical trial, regulatory, analytical, communication, and vendor-management expertise.
Kiniksa PharmaceuticalsNASDAQ: KNSA: Developing and commercializing therapies for cardiovascular and inflammatory diseases.
7+ YOEBachelor’s degree in health or biological science; 7+ years clinical operations with global trials; 3+ years as a clinical study lead or project manager; cardiovascular/rare disease experience preferred.
Electronic Data Capture (EDC), IRT, Clinical trial management software, Microsoft Office
Glattbrugg or King of Prussia or Maidenhead or Waltham
$170k-$201k/yrHybridFull Time
CSLASX: CSL: Global biotechnology producing plasma-derived and recombinant therapies.
8+ YOEBachelor’s degree, 8+ years in clinical operations, outsourcing, vendor management, or biotech/pharma business operations, plus FSP oversight, clinical trial, financial, and analytical experience.
Senior Manager, Clinical Project Management (Center Valley, PA, US, 18034-0610)
Center Valley or Westborough or Tokyo or United States
$120k-$168k/yrRemoteFull Time
OlympusTokyo Stock Exchange: 7733: Manufactures medical endoscopes and minimally invasive surgical tools.
12+ YOE3+ MgmtBachelor's in health sciences (or equivalent) plus 12+ years clinical trial management experience, 3+ years managing teams, expertise in clinical regulations (GCP/ICH/FDA), budget/scope management, EDC and Microsoft Office proficiency, ability to travel up to 40% domestically and ~10% internationally.
Electronic Data Capture, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Project
Zenas BioPharmaNASDAQ: ZBIO: Develops transformative therapies for patients with autoimmune diseases.
6+ YOEBachelor’s degree in life sciences or related field and 6+ years of clinical sample management experience. Requires vendor oversight, global trial experience, GCP familiarity, and strong operational and communication skills.
Good Clinical Practice (GCP), International Council for Harmonisation (ICH)
Tango TherapeuticsNasdaq Capital Market: TNGX: Develops precision cancer medicines using synthetic lethality principles.
5+ YOE5+ years trial management; 3+ years site management; Bachelor's degree in Life Sciences, Pharmacy, or related field; global clinical development experience; oncology preference; strong knowledge of ICH-GCP, FDA/EU guidelines; experience with trial systems and vendor oversight; travel flexibility.