NewSr. Oncology Clinical Research Associate JobotSr. Oncology Clinical Research AssociateNew York, NY$120,000–$140,000 / yearInformation collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. Conducts site visits including but not limited to Pre-study visits, initiation visits, interim monitoring visits, close-out visits to ensure compliance with protocols, Sponsor SOPs, ICH/GCP and all applicable regulations.
NewBilingual Registered Dietitian Clinical Research - PRN Professional Case ManagementBilingual Registered Dietitian Clinical Research - PRNNew York, NY$50–$50Performs the full scope of Registered Dietitian practices; including, but not limited to, providing virtual lifestyle counseling visits to improve nutrition and dietary quality, mental health and developing coping skills, and building health behavior and lifestyle habits that align with participant's goals and values. Please contact Ashley Sin at (303) 317-5486 x486 or at ashley.sin@emvenio.com today to learn more about our opportunities where you can make a difference in your own career!
NewRN Pediatric Clinical Research - PRN Professional Case ManagementRN Pediatric Clinical Research - PRNBayonne, NJ$60–$60Please contact Ashley Sin at (303) 317-5486 x486 or at ashley.sin@emvenio.com today to learn more about our opportunities where you can make a difference in your own career! Two (2) years' experience in starting and performing Phlebotomy/Peripheral Blood Draw, IVs, and Subcutaneous Injections (date of last practice within 6 months, preferred) .
NewSr. CRA (Oncology) Sponsor side! JobotSr. CRA (Oncology) Sponsor side!New York, NY$125,000–$140,000 / yearInformation collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners.
Clinical Solutions Manager- Informatics Medline IndustriesClinical Solutions Manager- InformaticsNew York City, NY$101,000–$152,000 / yearFull timeReviews and assesses applicable financial, clinical, and operational data, as well as evidence-based literature to assist teams in evaluating new supplies and new technology, using evidence based clinical data, benchmarked best practices and data driven analysis. Participate as a clinical team representative on project teams, committees and in meetings with various corporate departments to provide input as to the clinical perspectives on products and issues.
Medical Director, Sickle Cell Disease, Clinical Development Agios PharmaceuticalsMedical Director, Sickle Cell Disease, Clinical DevelopmentNew York, NY$221,600–$369,333 / yearThe current base salary range for this position is expected to be between $221,600 and $369,333 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators. Follow important developments and relevant trends in scientific literature and develop/maintain contracts with external experts to support understanding of the candidate drug effects and to gain strategic insights to the further development and placement of study and overall program.
NewClinical Director 4-2026 Hourchildren.orgClinical Director 4-2026Long Island City, NYPerform additional department or agency-related duties or special projects as directed by the supervisor, the Senior Director of Programs, Chief Impact & Program Officer, or Executive Director. Hour Children (HC) is an organization founded to help incarcerated and formerly incarcerated women and their children successfully rejoin the community, reunify with their families, and build healthy, independent, and secure lives.
NewStrategic Communications Lead – Pharma/Biotech IQVIAStrategic Communications Lead – Pharma/BiotechBrooklyn, NY$95,300–$237,500 / yearIn chosen areas of specialism (scientific or strategic), is capable of constructively challenging client thinking on a peer-to-peer level, producing novel points of view to help clients view potential solutions from new angles where appropriate and useful. Effectively leads client account teams setting the strategy (in partnership with Arc Bio Partners and clients), proactively reviews and evaluates progress, course correcting where necessary.
Oncology Clinical Research Associate (CRA) Zp Group LlcOncology Clinical Research Associate (CRA)NY$120,000–$135,000 / yearResponsibilities for the Oncology Clinical Research Associate: Monitor clinical trials to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Locations for the Clinical Research Associate: Wisconsin, Michigan, Illinois, Indiana, Ohio, Oklahoma, Nebraska, Utah, Colorado, New York and Massachusetts.
Senior Clinical Research Associate Zp Group LlcSenior Clinical Research AssociateNYRemote$155,000–$175,000 / yearKeywords: clinical research, clinical trials, CRA, oncology, general medicine, GCP, ICH, regulatory compliance, site monitoring, CTMS, EDC, patient recruitment, protocol training, clinical documentation, data review, query resolution, clinical operations, FDA regulations, SOPs, quality oversight, risk-based monitoring, therapeutic areas. Responsibilities of the Senior Clinical Research Associate include: Independently manage site monitoring activities for Phase II and III oncology trials, including a combination of onsite and remote visits averaging 8-10 onsite days per month.
Senior Clinical Research Associate I Zp Group LlcSenior Clinical Research Associate INYRemote$115,000–$125,000 / yearKeywords: clinical research, clinical trials, CRA, GCP, ICH, regulatory compliance, site monitoring, clinical monitoring, CTMS, EDC, cardiovascular studies, CNS trials, diabetes research, GLP-1, site management, FDA regulations, clinical operations, documentation, quality assurance, protocol compliance, investigator sites, patient safety, clinical development. Piper Companies is seeking a Senior Clinical Research Associate I to join a global organization within the clinical research and life sciences industry for a remote permanent role with 60-75% travel to sites in the US.
Clinical Research Associate - New York / New Jersey AstraZeneca PlcClinical Research Associate - New York / New JerseyNew York City, NY$112,154.40–$168,231.60 / yearIn addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). The CRA is responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with AZ Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the.
NewSenior Clinical Research Associate Protagonist TherapeuticsSenior Clinical Research AssociateNewark, New JerseySupport study vendor management by performing key activities as delegated by study CTM, including but not limited to: Participate in evaluation of new vendors (CROs, labs, central readers, EDC, etc.) by drafting and/or reviewing RFPs, analyzing responses and drafting work orders for select vendors • Manage the day to day interactions with select study vendor(s), such as a central or specialty lab including developing training materials, lab manuals and acting as first point of contact for issue and query escalation and resolution. Yes, up to 10% Core ResponsibilitiesOverall Study ExecutionPart of the clinical study team and takes a lead on execution by performing key activities as delegated by the Clinical Study lead, including but not limited to: Develop and/or review key study operational documents (e.g., study reference manual, laboratory and pharmacy manuals, data management plan, query generation, monitoring plan; review site audit reports) •.
Clinical Research Associate II - FSP Precision Medicine Group LLCClinical Research Associate II - FSPNY$91,500–$137,300 / yearEssential functions of the job include but are not limited to: Oversees all aspects of study site management to ensure patient safety is protected, quality of data generated by managed sites resulting in consistently low query levels and in acceptable Quality Assurance reports. Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs, Clinical Monitoring Plan/Site Management Plan and client requirements.
Senior Clinical Research Associate - CNS/Psychiatry - East Coast - Remote Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - CNS/Psychiatry - East Coast - RemoteNYRemote$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Phase I Oncology Clinical Research Associate Zp Group LlcPhase I Oncology Clinical Research AssociateNYRemote$110,000–$140,000 / yearKeywords: Phase One Oncology CRA, Clinical Research Associate, Phase I Oncology, First-in-Human Trials, Dose Escalation, Oncology Clinical Research, GCP, FDA Regulations, Clinical Monitoring, Biotechnology, Pharmaceutical. Piper Companies is seeking a Phase I Oncology Clinical Research Associate to support early-phase oncology clinical trials within the biotechnology and pharmaceutical industry.
Clinical Research Associate ICON PlcClinical Research AssociateNew York, NY$91,336–$114,170 / yearAs a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. Bonus, Com, Stock, Benefits & Disclaimer verbiage: Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level.
Senior Clinical Research Associate BeOne Medicines AGSenior Clinical Research AssociateNY$105,800–$140,800 / yearThe SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical study activities, departmental tasks, and provides mentoring to other CRA team members within established protocols and portfolio under general supervision. General Description: The SCRA is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs.
Clinical Research Associate II/III Novotech Health Holdings Pte LtdClinical Research Associate II/IIINY$70,000–$140,000 / yearPreferably experience of working in the research, pharmaceutical industry or a related field per job level as follows: CRA II: Approximately 1-2 years of Clinical Research Associate experience or equivalent experience (CRA II fast track) in other roles in the Clinical industry. Provide written and verbal site updates (including monitoring visit reports) on study progress to the PM/LCRA according to the study requirements/timelines as documented in the Clinical Monitoring Plan and Sponsor/Novotech SOPs.
Clinical Research Associate, Full Service IQVIA Holdings IncClinical Research Associate, Full ServiceParsippany, NJ$47,400–$169,300 / yearEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigators Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Senior Clinical Research Associate ICON PlcSenior Clinical Research AssociateNYRemoteFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Clinical Research Associate Novotech Health Holdings Pte LtdClinical Research AssociateNY$70,000–$110,000 / yearPreferably experience of working in the research, pharmaceutical industry or a related field per job level as follows: CRA II: Approximately 1-2 years of Clinical Research Associate experience or equivalent experience (CRA II fast track) in other roles in the Clinical industry. Provide written and verbal site updates (including monitoring visit reports) on study progress to the PM/LCRA according to the study requirements/timelines as documented in the Clinical Monitoring Plan and Sponsor/Novotech SOPs.
Clinical Research Coordinator * Oncology clinical research experience preferred * NYU Langone Medical CenterClinical Research Coordinator * Oncology clinical research experience preferred *New York, NY$70,481.60–$74,793.60 / yearThe Oncology CRC performs study coordination tasks under the direction of the principal investigator/treating investigator, under the supervision of the CTO management/leadership and works closely with the Oncology Clinical Research Nurses (CRNs), Oncology Clinical Research Coordinators (CRCs), Data Coordinator Unit (DCU) staff and other CTO and PCC staff to ensure patient safety, overall compliance in the conduct of the study, and adherence to the approved study protocol and quality clinical trial data collection. Schedules study participants according to the approved protocol; coordinates with ancillary service providers to ensure patients remain adherent to the protocol; coordinate subjects tests and procedures in compliance with the particular protocol and with the appropriate department, and collaborates with other NYU and PCC departments to seamlessly navigate a patient to a trial and through screening, treatment and follow up/end of treatment.
Inhouse Clinical Research Associate Novotech Health Holdings Pte LtdInhouse Clinical Research AssociateNY$65,000–$75,000 / yearCo-ordinate and maintain clinical study documentation in the Trial Master Files (TMF) including the tracking of documents, preparation for internal/external audits, conducting routine QC reviews and final reconciliation, according to the requirements of ICH GCP and Novotech (or client) SOPs. By offering trust, flexibility, and autonomy through programs like NovoLife, our flexible benefits framework, we empower team members to create an effective work-life balance that delivers professional satisfaction and maximum results for clients.
Senior Clinical Research Associate Novartis AGSenior Clinical Research AssociateNY$108,500–$201,500 / yearKey ResponsibilitiesLead assigned sites as the primary point of contact throughout study deliveryBuild strong relationships to ensure site performance, quality, and milestone achievementManage Phase I to Phase IV trials per monitoring plans and company proceduresConduct site initiation visits and deliver ongoing training for site personnelPerform remote and on-site monitoring to ensure compliance and patient safetyMaintain accurate documentation and update all clinical systems in a timely mannerIdentify risks, resolve issues, and escalate concerns as neededCollaborate with cross-functional teams to drive efficient study executionSupport timely data query resolution and ensure data accuracyAct as a subject matter expert across study activities when requiredEssential RequirementsMinimum of three years of clinical site monitoring experienceMinimum of Bachelor's degree in science, healthcare, or a related fieldStrong understanding of clinical research and drug development processesKnowledge of ICH/GCP and European regulatory requirementsAbility to manage multiple priorities and work independentlyStrong site management, communication, and problem-solving skillsFluency in written and spoken Czech/Slovak and EnglishAbility to travel extensively, up to 80% nationallyDesirable RequirementsExperience in radioligand therapy, chimeric antigen receptor T-cell therapy, or oncologyThe salary for this position is expected to range between $108,500 and $201,500 per year. Assigned to complex trials and/or less experienced sites, you may also act as a Subject Matter Expert, support audit and inspection readiness activities, ensure timely implementation of corrective actions, and collaborate with local and global cross-functional teams to drive process improvements that help bring innovative therapies to patients faster.
Senior Clinical Research Associate (Remote - Field Based) Novartis AGSenior Clinical Research Associate (Remote - Field Based)NYRemote$108,500–$201,500 / yearKey ResponsibilitiesLead assigned sites as the primary point of contact throughout study deliveryBuild strong relationships to ensure site performance, quality, and milestone achievementManage Phase I to Phase IV trials per monitoring plans and company proceduresConduct site initiation visits and deliver ongoing training for site personnelPerform remote and on-site monitoring to ensure compliance and patient safetyMaintain accurate documentation and update all clinical systems in a timely mannerIdentify risks, resolve issues, and escalate concerns as neededCollaborate with cross-functional teams to drive efficient study executionSupport timely data query resolution and ensure data accuracyAct as a subject matter expert across study activities when requiredEssential RequirementsMinimum of three years of clinical site monitoring experienceMinimum of Bachelor's degree in science, healthcare, or a related fieldStrong understanding of clinical research and drug development processesKnowledge of ICH/GCP and 21 CFR regulatory requirementsAbility to manage multiple priorities and work independentlyStrong site management, communication, and problem-solving skillsFluency in English, written and spoken, Spanish highly desiredAbility to drive and travel extensively, up to 80%, in a company vehicleDesirable RequirementsExperience in multiple therapeutic areas and Veeva Vault CTMS is a plus Advanced knowledge and use of AI The salary for this position is expected to range between $108,500 and $201,500 per year. Assigned to complex trials and/or less experienced sites, you may also act as a Subject Matter Expert, support audit and inspection readiness activities, ensure timely implementation of corrective actions, and collaborate with local and global cross-functional teams to drive process improvements that help bring innovative therapies to patients faster.
Research Administrative Manager (Executive Support & Research Operations) - Center for Interventional Cardiovascular Research and Clinical Trials Mount Sinai Health SystemResearch Administrative Manager (Executive Support & Research Operations) - Center for Interventional Cardiovascular Research and Clinical TrialsNY$65,193–$130,000 / yearMount Sinai advances health for all people, everywhere, by taking on the most complex health care challenges of our time - discovering and applying new scientific learning and knowledge; developing safer, more effective treatments; educating the next generation of medical leaders and innovators; and supporting local communities by delivering high-quality care to all who need it. We are consistently ranked by U.S. News & World Report's Best Hospitals, receiving high "Honor Roll" status, and are highly ranked: No. 1 in Geriatrics, top 5 in Cardiology/Heart Surgery, and top 20 in Diabetes/Endocrinology, Gastroenterology/GI Surgery, Neurology/Neurosurgery, Orthopedics, Pulmonology/Lung Surgery, Rehabilitation, and Urology.
Clinical Research Associate II, Oncology Pharmaron Beijing Co LtdClinical Research Associate II, OncologyNYRemote$90,000–$100,000 / yearWhat We are Looking for: Bachelor's degree, RN, or equivalent combination of education and relevant experience; life sciences background preferred 3+ years of clinical monitoring experience within sponsor, CRO, or investigative site environments Hands-on oncology monitoring experience required, including Phase I studies Strong knowledge of ICH-GCP guidelines and applicable regulatory requirements Ability and willingness to travel up to 30% based on study needs Excellent organizational skills with strong attention to detail Strong communication skills and ability to manage site relationships effectively Experience using CTMS, EDC, eTMF, and other clinical trial systems Experience in early-phase startup environments Ability to independently prioritize workload across multiple sites and studies Why Pharmaron? Position: Clinical Research Associate II, Oncology Location: Remote (East Coast USA Preferred) Salary: $90,000 to $100,000 D.O.E Unfortunately, we cannot support work visa permit applications for this role About Pharmaron Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life.
Clinical Research Coordinator Hackensack Meridian HealthClinical Research CoordinatorHackensack, New JerseySchedules, coordinates, prepares, and assists for all sponsor monitor site visits and ensures all supporting documentation records are adequate and available for the visit; Meets with monitor at least once during each monitor site visit and resolves all issues found during visit. Responsibilities: A day in the life of a Clinical Research Coordinator at Hackensack Meridian Health includes: Acts as liaison between principal investigators, sub-investigators, clinical research nurses and regulatory specialists on all regulatory issues and changes within the protocol.
Clinical Research Coordinator * Oncology clinical research experience preferred * New York University School of MedicineClinical Research Coordinator * Oncology clinical research experience preferred *NY$70,481.60–$74,793.60 / yearThe Oncology CRC performs study coordination tasks under the direction of the principal investigator/treating investigator, under the supervision of the CTO management/leadership and works closely with the Oncology Clinical Research Nurses (CRNs), Oncology Clinical Research Coordinators (CRCs), Data Coordinator Unit (DCU) staff and other CTO and PCC staff to ensure patient safety, overall compliance in the conduct of the study, and adherence to the approved study protocol and quality clinical trial data collection. Schedules study participants according to the approved protocol; coordinates with ancillary service providers to ensure patients remain adherent to the protocol; coordinate subjects tests and procedures in compliance with the particular protocol and with the appropriate department, and collaborates with other NYU and PCC departments to seamlessly navigate a patient to a trial and through screening, treatment and follow up/end of treatment.
Clinical Research Associate Alira HealthClinical Research AssociateNY$125,000–$145,000 / yearQuality focused; Proven ability to be careful, thorough, and detail-oriented Strong organizational skills and the ability to multi-task and work effectively in a fast-paced environment Able to manage priorities, organize time and solve problems Strong analytical, negotiation, meeting management, cross-functional team, and leadership skills Ability to travel Ability to manage stress Professional, trustworthy and disciplined Ability to problem-solve unstructured or ambiguous challenges Strong command of Local language, both written and verbal, in the country where monitoring activities are performed Excellent communication and interpersonal skills with customer service orientation Good computer skills, with ability to use clinical trial management systems, clinical trial databases and electronic data capture Self-starter who thrives in a collaborative, yet less structured team environment Knowledge of clinical research, ICH GCP and local regulations Knowledge of Regulatory and Ethical requirements EU: Adequate English. • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work, Alira Health SOPs and regulatory requirements, i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) Guidelines.
Clinical Research Associate - Sponsor Dedicated IQVIAClinical Research Associate - Sponsor DedicatedParsippany, KansasEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Senior Clinical Research Associate EBR Systems IncSenior Clinical Research AssociateNY$108,700–$139,800 / yearThe Senior CRA works in close collaboration with EBR Field Clinical Engineering, proactively removes barriers to study execution, interprets clinical data in context, and ensures issues are identified and escalated early to protect data quality, timelines, and regulatory outcomes. Beyond traditional monitoring, the Senior CRA serves as a trusted clinical partner at the site level-cultivating strong investigator and coordinator relationships, actively supporting enrollment and follow-up performance, and engaging with site teams on the clinical substance of the work, not just operational logistics.
Clinical Research Associate - Cell Therapy AstraZeneca PlcClinical Research Associate - Cell Therapy$112,154.40–$168,231.60 / yearThe CRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies in compliance with AstraZeneca Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations, ensuring that sites deliver according to study commitments. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles).
Senior Clinical Research Associate Danaher CorpSenior Clinical Research AssociateNYRemote$103,000–$130,000 / yearContribute to study planning including budget and contract negotiation and timeline forecasts, site identification and qualifications, and process improvement initiatives within the Global Clinical Affairs organization; as well as prepare study documents, including creating clinical templates, such as informed consent forms, clinical monitoring plan, etc. Conduct independent study monitoring, including site coordination, investigational product accountability, and assessments of protocol deviations and/or adverse events, and drive clinical data quality which can include follow up on incomplete data entry and/or outstanding queries.
Sr. Clinical Research Associate Danaher CorpSr. Clinical Research AssociateNYRemote$103,000–$130,000 / yearContribute to study planning including budget and contract negotiation and timeline forecasts, site identification and qualifications, and process improvement initiatives within the Global Clinical Affairs organization; as well as prepare study documents, including creating clinical templates, such as informed consent forms, clinical monitoring plan, etc. Conduct independent study monitoring, including site coordination, investigational product accountability, and assessments of protocol deviations and/or adverse events, and drive clinical data quality which can include follow up on incomplete data entry and/or outstanding queries.
Clinical Research Nurse - Phase 1 - P/T with Benefits - Days Hackensack Meridian HealthClinical Research Nurse - Phase 1 - P/T with Benefits - DaysHackensack, New JerseyResponsibilities: Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential. Performs nursing assessments and monitors study patient`s progress during clinical trials; Tracks study patient`s response by documenting on toxicity flow sheet, medication flow sheet and nurses` progress notes.
Senior Clinical Director, Clinical Research, Hematology Merck & Co IncSenior Clinical Director, Clinical Research, HematologyNJ$282,200–$444,200 / yearThe Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area, specifically in our Hematology Section. The Senior Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies.
Clinical Research Nurse Hackensack Meridian HealthClinical Research NurseParamus, New JerseyFull timeAssists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential. Performs nursing assessments and monitors study patient`s progress during clinical trials; Tracks study patient`s response by documenting on toxicity flow sheet, medication flow sheet and nurses` progress notes.
Clinical Research Coordinator * Must have experience with oncology clinical trials * NYU Langone Medical CenterClinical Research Coordinator * Must have experience with oncology clinical trials *New York, NY$70,481.60–$74,793.60 / yearThe Oncology CRC performs study coordination tasks under the direction of the principal investigator/treating investigator, under the supervision of the CTO management/leadership and works closely with the Oncology Clinical Research Nurses (CRNs), Oncology Clinical Research Coordinators (CRCs), Data Coordinator Unit (DCU) staff and other CTO and PCC staff to ensure patient safety, overall compliance in the conduct of the study, and adherence to the approved study protocol and quality clinical trial data collection. Schedules study participants according to the approved protocol; coordinates with ancillary service providers to ensure patients remain adherent to the protocol; coordinate subjects tests and procedures in compliance with the particular protocol and with the appropriate department, and collaborates with other NYU and PCC departments to seamlessly navigate a patient to a trial and through screening, treatment and follow up/end of treatment.
Clinical Research Support Assistant Full Time Day Clinical Trials The Valley HospitalClinical Research Support Assistant Full Time Day Clinical TrialsParamus, NJ$21.90–$27.37 / hourShort-term and Long-term Disability, Whole Life Insurance, Legal Support, etc.) • 6 Paid Holidays, Paid Time Off (varies), Wellness Time Off, Extended Illness • Retirement Plan • Employee Assistance Program (EAP) • Valley Health LifeStyles Fitness Center Membership Discount • Day Care Discounts for Various Daycare Facilities. The Clinical Research Support Assistant provides support to the clinical research team by maintaining study inventory, assisting with biospecimen collection and processing, and supporting logistics related to clinical trial conduct.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedParsippany, NJEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Clinical Research Associate - Sponsor Dedicated IQVIA Holdings IncClinical Research Associate - Sponsor DedicatedParsippany, NJEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Clinical Research Associate, Sponsor Dedicated, Oncology or Immunology IQVIA Holdings IncClinical Research Associate, Sponsor Dedicated, Oncology or ImmunologyParsippany, NJ$69,800–$226,800 / yearJoin our team as a Clinical Research Site Manager, where you'll play a crucial role in ensuring our study sites operate seamlessly and adhere to all protocols, regulations, and sponsor requirements. Documentation: Ensure all site documents are filed in the Trial Master File (TMF) and Investigator's Site File (ISF) according to GCP/ICH and local regulations.
NewSenior Clinical Research Manager Columbia UniversitySenior Clinical Research ManagerNew York, NY$115,000–$125,000 / yearThis role expands upon the Clinical Research Manager (CRM) position by incorporating higher-level leadership, strategic planning, financial oversight, and departmental initiatives. The Senior Clinical Research Manager reports to the Assistant Director, Clinical Research Operations and is primarily based out of 161 Fort Washington Avenue, New York, NY.
Associate Clinical Research Coordinator - Cancer Center Clinical Trials - Mineola NYU Langone Medical CenterAssociate Clinical Research Coordinator - Cancer Center Clinical Trials - MineolaMineola, NY$66,300–$68,250 / yearUnder direct supervision, collaborate with various NYU School of Medicine and Hospital personnel involved in assisting with specific aspects of each study that may include: Research Nurses, Infusion Nurses, Phlebotomists, Program Managers, Regulatory staff and collaborating NYU Laboratories. The aCRC performs study coordination tasks under the direction of the investigator and works closely with the Research Nurse, other CRCs and the collaborating CTO units for the Disease Management Group(s) to ensure overall compliance in the conduct of the study and adherence to the approved study protocol.
Clinical Research Associate I (East Coast: NY, FL, NJ, PA, OH, DC, MD) Premier Research International LLCClinical Research Associate I (East Coast: NY, FL, NJ, PA, OH, DC, MD)NJYou will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. Premier Research is looking for a Clinical Research Associate I (East Coast: NY, FL, NJ, PA, OH, DC, MD) to join our Global Clinical Monitoring and Site Management team.
Clinical Director (Principal Scientist), Clinical Research, Immunology - Rheumatology Merck & Co IncClinical Director (Principal Scientist), Clinical Research, Immunology - RheumatologyRahway, NJ$255,800–$402,700 / yearThe Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within their area of expertise, in terms of new scientific findings, research methodologies. Job Description: The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Immunology therapeutic area.
Clinical Director, Clinical Research, Hematology Merck & Co IncClinical Director, Clinical Research, HematologyNJ$255,800–$402,700 / yearThe Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies. The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area, specifically in our Hematology Section.
Clinical Research Nurse - Phase 1 - F/T - Days Hackensack University Medical CenterClinical Research Nurse - Phase 1 - F/T - DaysHackensack, NJHackensack Meridian Health nurses care for patients and their families at every stage of life, 24 hours a day, at bedsides in 9 community hospitals, 4 academic medical centers, a behavioral health hospital, 2 children's hospitals, 2 rehabilitation hospitals, medical offices, and care facilities across the state. Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential.