NewClinical Trial Associate Janux Therapeutics IncClinical Trial AssociateSan Diego, CA$105,000–$115,000 / yearThis individual will be responsible for coordinating study documentation, maintaining inspection-ready Trial Master Files (TMFs), tracking study metrics, supporting study start-up and closeout activities, and facilitating communication among cross-functional stakeholders. The CTA will partner closely with Clinical Trial Managers, Clinical Operations leadership, CROs, study vendors, and investigative sites to ensure studies are conducted in compliance with protocol requirements, ICH/GCP guidelines, regulatory requirements, and internal SOPs.
Clinical Trial Lead Menarini GroupClinical Trial LeadNew York, New York$218,286–$250,000 / yearThanks to the valuable contribution of around 18,000 employees, every year more than 500 million packs of drugs are produced at the Group's 18 manufacturing sites including a biotech plant for the manufacturing of monoclonal antibodies that also serves external clients distributed across 6 continents. Following a successful phase 3 study, Menarini Stemline received FDA approval in January 2023 under priority review and successfully oversaw a strong launch in February to the US market with the EMA review process concluded positively in September 2023.
NewClinical Trial Associate I AbbottClinical Trial Associate IMadison, WisconsinProficient in using basic software applications including Microsoft Office (Word - generate documents and tables, Excel - create and modify spreadsheets, create complex formulas, etc., Email – preferably Outlook) and various search engines for conducting Internet searches. Maintain a working understanding of current SOPs, work instructions, applicable regulations, and guidance documents, such as FDA Code of Federal Regulations (CFR) and International Council on Harmonisation (ICH), Guideline for Good Clinical Practices (GCP).
Clinical Trials Associates Intern Worldwide Clinical Trials Holdings IncClinical Trials Associates InternNC$32,000–$64,000 / yearWithin this intern role you are responsible for providing administrative and project training support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed in a timely and accurate manner. SUMMARY: The Intern position was created to allow for Juniors, Seniors or post-graduate students in an accredited University to gain valuable hands-on experience in their chosen field as well as the opportunity for real-world work experience.
Clinical Trials Associate II Glaukos CorpClinical Trials Associate IIAliso Viejo, CAOur constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra "We'll Go First," which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do. Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients.
NewClinical Trials Consultant Attain PartnersClinical Trials ConsultantWe are looking for experienced professionals with a background in clinical trial billing and systems, CTMS builds, regulatory support, budget negotiations, and process improvement to work in a consulting environment serving research institutions. Our comprehensive benefits package starts on your first day of employment and includes benefits such as: Competitive health, dental, and vision coverage, HSA and FSA accounts, life and disability insurance, fertility and family planning benefits, and employee assistance and discount programs.
NewBroker II, Life Sciences | Clinical Trials Liability Aon PlcBroker II, Life Sciences | Clinical Trials LiabilityPhiladelphia, PA$110,000–$135,000 / yearSkills and experience that will lead to success Unlike most insurance programs, the primary purpose of Clinical Trial Liability insurance is to support Pharma and Biotech companies through regulatory approvals and contractual compliance while simultaneously protecting these trial sponsors and their research partners from financial liability in case of injury or harm. What the day will look like Responsible for broking/placing primarily Clinical Trials Liability as well Products Liability, Errors & Omissions Liability, and Excess Liability Market new and renewal business, handling all aspects of the placements from initial market selection through the long-term servicing until the clinical trials these policies are covering are over.
NewAdministrative Assistant, Research - Clinical Trials, Full Time, Day The Valley HospitalAdministrative Assistant, Research - Clinical Trials, Full Time, DayProvides high-level administrative and operational support to Valley Health System’s research leadership, including the Medical Director of Research, Director of Research Operations, and Manager of Clinical Trials & Research. Requires Associates Degree in Office Management, Business Administration or High School diploma or equivalent and completion of formation course work in secretarial science or related field.
Medical Writer - Perlmutter Cancer Center Clinical Trials Office NYU Langone Medical CenterMedical Writer - Perlmutter Cancer Center Clinical Trials OfficeNew York, NY$84,577.92–$88,200 / yearThe Medical Writer provides support for all Investigator Initiated Trials (IIT) at the Perlmutter Cancer Center (PCC) across all campuses and report into the Protocol Development Monitoring Unit (PDMU) at the Clinical Trials Office (CTO) with a reporting line to the PCC Molecular Oncology program. Additionally, all employees have access to our holistic employee wellness program, which focuses on seven key areas of well-being: physical, mental, nutritional, sleep, social, financial, and preventive care.
Clinical Trials Market Research-SW Ohio Wesleyan UniversityClinical Trials Market Research-SWDelaware, OHPurpose/Objective of the Role: Clinical Research Delivered, Inc. (CRD) is a healthcare startup with a mission to accelerate the delivery of life-changing medical innovations by bringing clinical research visits directly to study subjects-in their homes and communities at convenient times-improving subject retention, trial completion and speed to market. The intern will support a focused market research and marketing outreach project that explores clinical trial participation from the study participant's perspective and translates findings into practical marketing content for sponsors and Clinical Research Organizations (CROs).
Business Development Representative (Clinical Trial SaaS) ProofPilot, Inc.Business Development Representative (Clinical Trial SaaS)Raleigh, NC$50,000–$70,000The Business Development Representative (BDR) is a high-impact, high-visibility role responsible for generating and qualifying new business opportunities with clinical operations, feasibility, and digital innovation leaders at pharmaceutical and biotechnology sponsors. Clearly articulate ProofPilot's differentiated value proposition: white-label branding, true end-to-end platform, holistic patient and site journey visibility, and GxP compliance.
Business Development Representative (Clinical Trial SaaS) (Remote) ProofPilot, Inc.Business Development Representative (Clinical Trial SaaS) (Remote)Raleigh, NCRemoteThe Business Development Representative (BDR) is a high-impact, high-visibility role responsible for generating and qualifying new business opportunities with clinical operations, feasibility, and digital innovation leaders at pharmaceutical and biotechnology sponsors. Clearly articulate ProofPilot's differentiated value proposition: white-label branding, true end-to-end platform, holistic patient and site journey visibility, and GxP compliance.
Clinical Trial Navigator I (PRN) JavaraClinical Trial Navigator I (PRN)Ensure scientific integrity of data and record source data appropriately and accurately inclusive of patient visit data within source, CTMS, electronic reporting systems, completing the sponsor’s case report form, and timely query resolution. Javara brings better outcomes for patient centered care, better economic results, improved access to cutting edge therapies and a more predictable research delivery model to the biopharmaceutical sector.
Senior Clinical Trial Liaison (US) Worldwide Clinical Trials Holdings IncSenior Clinical Trial Liaison (US)Miami, FL$134,500–$267,500 / yearClinical Trial Liaison will serve in part as a Strategic Site Relationship Manager, establishing and maintaining strong relationships with clinical investigators and site staff within their therapeutic areas of expertise and providing insights to internal teams and sponsors, with an overall focus on successful trial execution. The Clinical Trial Liaison will also assist with the overall remit for Scientific Solutions, ensuring quality endpoints are achieved through optimal site selection and assisting sites with understanding of protocols and enrolment of proper trial participants.
Clinical Trial Liaison Worldwide Clinical Trials Holdings IncClinical Trial LiaisonNC$134,500–$267,500 / yearThe Clinical Trial Liaison will serve in part as a Strategic Site Relationship Manager, establishing and maintaining strong relationships with clinical investigators and site staff within their therapeutic areas of expertise and providing insights to internal teams and sponsors, with an overall focus on successful trial execution. A doctoral degree is required, or alternatively, a candidate may possess a bachelor's/master's degree accompanied by experience as an advanced practice provider, such as a Physician's Assistant, Nurse Practitioner, or another licensed healthcare provider.
Assistant Clinical Trial Navigator (Temporary) JavaraAssistant Clinical Trial Navigator (Temporary)Charlotte, North CarolinaEnsure scientific integrity of data and record source data appropriately and accurately inclusive of patient visit data within source, CTMS, electronic reporting systems, completing the sponsor’s case report form, and timely query resolution. Javara brings better outcomes for patient centered care, better economic results, improved access to cutting edge therapies and a more predictable research delivery model to the biopharmaceutical sector.
Assistant Clinical Trial Navigator JavaraAssistant Clinical Trial NavigatorSavannah, GeorgiaEnsure scientific integrity of data and record source data appropriately and accurately inclusive of patient visit data within source, CTMS, electronic reporting systems, completing the sponsor’s case report form, and timely query resolution. Javara brings better outcomes for patient centered care, better economic results, improved access to cutting edge therapies and a more predictable research delivery model to the biopharmaceutical sector.
Investigator Initiated Trial Research Operations Project Manager Commonwealth of VirginiaInvestigator Initiated Trial Research Operations Project ManagerRichmond, VAResearch Administrators often serve as a key point of contact between the university and the research sponsor, research project staff, and participants, ensuring effective coordination and communication across all stakeholders involved in study development and conduct; Maintain systems and processes for managing at both a project and a program level, including development and tracking of project timelines, study start-up activities, and key study milestones; Work closely with Principal Investigators (PI), study staff, unit administrators, and coordinate with central offices in pre and/or post award stages of project management; as well as providing research program level reporting and analytics to leadership, while facilitating cross-functional coordination (e.g., regulatory, data management, and clinical operations) to support study activation and ongoing execution; Support and coordinate study start-up activities, including feasibility assessment, site readiness, and activation planning, ensuring studies are prepared for timely execution; Oversee and coordinate activities across participating sites or teams, ensuring consistency in study conduct and timely resolution of issues; Identify potential risks, delays, or gaps in project execution and proactively implement mitigation strategies; Track and report study progress, including key milestones such as activation, enrollment, and study completion, to support leadership oversight and decision-making; Other duties as assigned. Bachelor"s degree or equivalent applicable combination of training, education and experience required; Candidates whose resumes highlight the following previous experience will be prioritized: Demonstrated experience working in and fostering an environment of respect, professionalism and civility with a population of faculty, staff, and students from various backgrounds and experiences, or a commitment to do so as a staff member at VCU; Advanced proficiency with data entry and word processing skills, with the ability to analyze and interpret information effectively; Advanced organizational abilities and a keen eye for detail to ensure accuracy and efficiency in all tasks with the ability to multitask and prioritize autonomously; Clear and professional written and verbal communication skills, with the ability to interact effectively with colleagues and stakeholders; Interpersonal skills, capable of building relationships and collaborating with team members at all levels to gather information and support compliance efforts; Problem-solving and organizational aptitude, with the ability to manage multiple tasks, meet deadlines in a dynamic environment and independently make critical decisions.
Clinical Trials Regulatory Specialist 2 (Remote Opportunity) Stanford UniversityClinical Trials Regulatory Specialist 2 (Remote Opportunity)CARemoteYou will engage with company sponsors, clinical research organizations, Stanford investigators and their study teams, the Stanford Institutional Review Board (IRB), other external IRBs, the FDA, and various regulatory authorities, as well as any other entities that contribute to clinical research at our institution. CRH is seeking a mission-driven Clinical Trials Regulatory Specialist 2. In this role, you will collaborate with a high-performing team of clinical operations staff and medical experts.
Clinical Project Manager PSI CRO AGClinical Project ManagerTake your career to the next level and lead challenging full-service clinical research projects in phase II and III, managing the full scope of responsibilities and getting hands-on involvement in every aspect of the study. PSI is a leading Contract Research Organization with 30 years in the industry offering a perfect balance between stability and innovation to both clients and employees.