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Job Description Job Title: Clinical Research Coordinator Position Summary: The Clinical Research Coordinator is responsible for facilitating and overseeing radiology and tumor response assessments for assigned clinical trials. This role plays a key part in planning, coordinating, and implementing workflows in compliance with all relevant local, federal, and state regulations, as well as institutional policies and standard operating procedures. Working under the general supervision of the principal investigator, radiologists, and study teams, the coordinator conducts radiology research and serves as a vital liaison between the Cancer Center and the Radiology Department. Key Responsibilities: • Coordinate and manage radiology and tumor response assessments for clinical trials., • Ensure compliance with regulatory requirements and institutional SOPs., • Collaborate with principal investigators, radiologists, and study teams to support trial execution., • Serve as the primary point of contact between the Cancer Center and Radiology Department., • Maintain accurate documentation and records related to clinical trial activities. Required: • Bachelor’s degree in a science or healthcare-related field., • Minimum of 2 years in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years of related experience in clinical research., • Strong attention to detail and a customer service-oriented mindset., • Ability to work independently and collaboratively in a fast-paced, deadline-driven environment., • Excellent organizational, presentation, documentation, and interpersonal skills., • Strong written and verbal communication abilities., • Education or training in human subject research and Good Clinical Practice (GCP)., • Professional certification such as:, • SOCRA Certified Clinical Research Professional (CCRP), • Certified Clinical Research Associate (CCRA) This is a Permanent position based out of Hackensack, New Jersey. Pay and Benefits The pay range for this position is $80000.00 - $80000.00/yr. HMH perm benefits are offered Workplace Type This is a fully onsite position in Hackensack,NJ. Application Deadline This position is anticipated to close on Oct 30, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job Description Clinical Supplies Manager Paramus, NJ Clinical Supplies Manager Paramus, NJ Experience level: Mid-senior Experience required: 8 Years Education level: Bachelors degree Job function: Management Industry: Pharmaceuticals Pay rate : View hourly payrate Total position: 1 Relocation assistance: No Visa sponsorship eligibility: No SUMMARY OF POSITION: Assist and support the Associate Director in managing Contract Development and Research Organizations (CDMO) in the areas of Clinical Supplies. Review master batch records (MBR), Master Packaging Work Orders (MPWO), and clinical related supplies-related documents. Assist and support the review of packaging, labeling, storage, logistics, and distribution documentation of the investigational product. Assist and support the management of clinical supply inventories using Interactive Response Technology. Expected to prepare data tables when needed for data interpretation. Assist with documentation and process internal and external change controls. Assist and support clinical supply activities for investigational products, such as import and export, customs clearance, DEA Controlled Drug experiences, etc. Manage and processing of CMC Team project invoices and internal project budget requests (ARIBA), and monitoring of project financial tracking. Assist and support Regulatory Affairs (RA) to provide any documents for their submissions (US and Global). Assist and support the Quality Assurance Unit (QAU) regarding the review of investigations and conduct vendors and internal audits. Assist and support Clinical Operations on document reviews related to KEY RESPONSIBILITIES: Technical Management Assist collaborated team to prepare clinical supplies request forms for new and existing studies when its need it. Prepare requests for proposals for activities in support of clinical supply projects. Review CDMO Project proposals and provide feedback to the Associate Director before selecting a specific vendor, review and audit slides, tables, and budget calculations. Assist and prepare CDMO Vendor Comparison slides and assist in the selection of an appropriate CDMO based on technical ability, cost, and ability to deliver on time. Provide technical support for vendors IRT/IWRS system in support of SK clinical studies. Utilize inventory forecasting software to ensure an adequate amount of CTMs is available to supply clinical sites when needed. Assist and support in writing and preparation of regulatory submission documents: drug product and drug substance sections in IND, Annual reports, and Informational amendments. Assist and support in writing and preparation of SOPs and interpreting and reviewing SOPs and study protocols. Review manufacturing, packaging, and labeling Master and Executed Packaging Work Orders/Batch Records (MBR/EBR, Packaging Labeling Approval Forms (PLAF), Labeling Approval Forms (LAF), etc. Assist and prepare Excel tables when needed. Assist in the maintenance of SOPs related to reflecting current clinical supply activities. Assist and support Investigational Product Returns and Reconciliation at the end of the studies and collect all necessary documentation from vendors. Financial Management Prepare Ariba process for internal budget approval of new/ongoing CMC Team projects. Prepare, maintain, and monitor project budgets for the CMC Team Review and process clinical supply CMO invoices for project activities. Prepare and assist the FP&A team on project-specific spending and accrual monthly and quarterly basis, if requested. Participate in project budgeting and forecasting process for the CMC Teams annual project budget management activities. QUALIFICATIONS: Bachelors degree in chemistry (preferred analytical) and up to 5-8 years of experience working in an analytical laboratory background. Ability to read, analyze, and interpret basic scientific protocols, reports, and technical journals. Also, should be able to interpret financial reports. Expert technical skills, good organization skills, ability to follow directions, and good communication skills. Computer aptitude is a plus, especially proficiency with Microsoft Office, and in particular use of Excel and the ability to plot data. Understand protocols, write SOPs, and have technical knowledge of packaging and labeling activities. Knowledge of pharmaceutical stability protocols, assessment of expiration dating for investigational drug products Knowledge of GMP batch record development, review, and approval process Demonstrated understanding of the entire supply chain and associated cost drivers Ability to execute the Clinical Supply portion of User Acceptance Testing (UAT) for the IRT system. Knowledge of GCP and global cGMP regulations, (knowledge of EU GMP QP regulations is preferred), a plus. Knowledge of warehousing, distribution (including cold chain distribution), and logistics, a plus. Ability to review, analyze, and interpret the IVR/IRT reports and specification requirements, a plus. Ability to understand, maintain, and demonstrate troubleshooting on vendors IRT/IVRS system, a plus.

Responsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions. Under the direction of supervisor or designee, this position will serve

The ideal candidate for our Clinical Research Associate - Qualitative Methods position will conduct both qualitative research and prepare high-quality clinical study documentation, including protocols, method validation reports, and scientific publications. Job Description: Develop and implement qua

In addition to clinical responsibilities, faculty members may have opportunities to participate in clinical, translational, or population-based research, as well as the teaching of medical students, residents, and fellows.

Job Description: Provide project management and operational support to designated clinical project team ensuring that quality, timelines, and project specifications are met Manage study documentation ensuring accuracy within the documentation while aiding in the preparation of supply shipments to st

Prior work experience must include one (1) year of experience (with a Master’s) or three (3) years of experience (with a Bachelor’s) in the following: performing quantitative and qualitative analysis and communicating concise information for internal and external stakeholders at various levels o

Access to cutting-edge technology and research opportunities.

Radiology physician employment in New York : Whether you are looking for a new telehealth opportunity or a way to supplement your income, CompHealth can help you find an assignment to meet your needs.Weekdays, Weekends, Days, 12-hour shifts.CT, PF, US, MR, and nuclear medicine.We negotiate better pa

Associate Program Director - Pathology Residency Program Westchester County, NY Mon-Fri 8:30am-5pmThe prospective candidate will collaborate with the current Program Director to administer and maintain a residency program that is conducive to exceptional clinical learning and professional developmen

The Department of Dermatology at Columbia University Vagelos College of Physicians & Surgeons is seeking a new or mid-career physician as Assistant Clinical Dermatologist or a seasoned physician as Associate Clinical Dermatologist. The Associate Clinical Dermatologist will exhibit sustained excellen

The New York Obesity Research Center, within the Division of Endocrinology, is seeking a Clinical Research Associate to support the technical aspects of a clinical trial focused on obesity and type 2 diabetes. The incumbent will be responsible for biospecimen collection, processing, and shipment to

Pinnacle Clinical Research is seeking a Full-time Geriatrician to serve as a Principal Investigator (PI) for clinical trials. Responsibilities include providing clinical oversight, monitoring patient safety, and collaborating with research staff to advance clinical studies. Ideal candidates will hav

The Brain Donation Coordinator in the Division of Aging & Dementia and in the Taub Institute for Research on Alzheimer's Disease and the Aging Brain at Columbia University Irving Medical Center will be working as part of several federally funded research projects which follow aging persons who inten

The position includes an academic appointment with Columbia University Vagelos College of Physicians and Surgeons, one of the top-ranked multidisciplinary clinical and research teams in the country.

Understanding operational metrics and how clinical excellence can impact clinical operations. Ability to analyze clinical opportunities, strategically plan, and implement clinical programs and initiatives. The DCE develops and supports the organization in clinical analysis, education, training, and

NewYork-Presbyterian Medical Group.Board Certified/Board Eligible Endocrinologist .NewYork-Presbyterian Medical Group/Hudson Valley’s ambulatory offices located in Croton-on-Hudson, New York.The practice site is located in close proximity to.NewYork-Presbyterian/Hudson Valley Hospital.NewYork-Pre

The Clinical Research Director (CRD) provides medical and scientific expertise to the creation and implementation of global clinical development plans and other activities within Sanofi Genzyme related to the corporate mission of developing novel and valued therapeutics for patients with high unmet

At least 2 years of experience in clinical research or human subjects research required. SOCRA Certified Clinical Research Professional (CCRP) or ACRP Certified Professional (ACRP-CP/CCRC) preferred. Schedule participant visits, imaging procedures, and follow-up assessments; coordinate logistics wit

Research Senior Associate for its New York, NY location. Deliver investment advice and insights to institutional investors, corporations, and other research recipients. Conduct market and industry qualitative and quantitative research for technology, market, and competitive due diligence within the

The Clinical Research Coordinator manages clinical trials (including some regulatory and budget requirements) and assists in the coordination of tests/visits for patients, working with the study team to maximize work efficiency to gather all required data and relevant clinical information. Director

The Senior Clinical Study Lead (CSL) is expected to operate with a high degree of independence and is accountable for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out. This role applies to internally sourced studies and st

The CRC will work with investigators, study staff, Scientific Review Committee (SRC) and institutional review boards (IRB), clinical trial sponsors and federal regulatory agencies to assure compliance with study protocols, data documentation, reporting requirements, ensure that regulatory requiremen

Works with minimal oversight from the Clinical Operations Senior Director or Director, in collaboration with Clinical Study Management teams and Clinical Research and Development functional teams. Clinical Operations, Project & Portfolio Management, Clinical Research). The successful candidate will

Responsible for researching products/potential vendors, researching/procuring study supplies, monitoring inbound shipments and cost accruals per study. A minimum of 3 years' experience in Medical Device clinical trials, pharmaceutical, biotechnology or related firm, including direct exposure to the

The focus of the Clinical Sales Associate (CSA) is to clinically sell to maximize the da Vinci Surgical System's utilization in the Manhattan, NYC territory. Additional job duties may be determined by functional people manager) Work with the Clinical Sales Manager to develop a sales strategy to driv

The Columbia University Division of Infectious Diseases is seeking a dedicated Clinical Research Coordinator to join our team advancing cutting-edge HIV, HIV prevention and sexual health, and emerging infections research. Experience in infectious disease clinical care and/or research. Develop and ma

At least 2 years of experience in clinical research or human subjects research required. Schedule participant visits, imaging procedures, and follow-up assessments; coordinate logistics with research staff and clinical teams. Clinical Research Coordinator - Careers At East River Medical Imaging, PC.

The Clinical Research Manager I (CRM I) is a professional who oversees and coordinates the execution of clinical research studies and trials. This CRM I supervises Clinical Research Coordinators and ensures accountability to Cardiology Research guidance documents and standard operating procedures. P

Prior experience in clinical research and/or in research billing compliance required. A working understanding of research billing compliance including National Coverage Determinations (NCCDs) for coverage of routine costs and the CMS Clinical Research Policy required. We have an exciting opportunity

The clinical research aide will perform a variety of research duties in support of funded studies related to maternal-child health. Early childhood/pregnant women research or clinical experience. The responsibilities for the position include: recruiting study participants, screening potential partic

This position champions Clinical Excellence by monitoring patient outcomes, treatment protocols, documentation quality, and adherence to best practices to drive high-quality patient care. Experienced teammates are encouraged to become certified clinical instructors and mentor students.

Clinical Research Coordinators (CRCs) are key members of research teams at Columbia. Knowledge of clinical research systems and processes, Good Clinical Practice (GCP) guidelines, HIPAA, IRB and other regulatory and compliance activities. Adhere to workplace and patient safety protocols, monitor the

Metro PT is looking for a motivated, compassionate, forward-thinking Clinical Director for our brand new Harrison location! If you're an experienced Physical Therapist ready to take the next step forward in your career, we want to hear from you! Our clinics enjoy a well-trained support staff, as wel

Under the direction of the Project Coordinator II and the Principal Investigator, the Clinical Research Coordinator (CRC) will be responsible for coordinating the day-to-day activities of a laboratory-based research protocol focused on examining the health benefits of breaking up periods of prolonge

Provides clinical instruction, mentoring, and direction to PTA’s, and Students as assigned. Will provide orientation and clinical guidance to new team members as needed. Experience in clinical practice across a range of settings preferred (e.

The Associate Research Scientist's responsibilities will consist of working closely with members in the Pediatric Cardiology Heart Center Research Core, providing senior level biostatistical and analytic support for all projects. Conduct applied research in an area of considerable scope of complexit

Clinical Territory Associate- Future Opportunity. CTA) is a 24+ month developmental role that will partner with the Ft Wayne team to gain knowledge in all aspects of our business to include technical, clinical, and sales.

The role of a Clinical Research Coordinator may support task-oriented requirements within the broader context of clinical research coordination. The Clinical Research Coordinator I (CRC I) is responsible for independently coordinating simple to moderately complex clinical research studies, including

Desire to be part of a strong team that emphasizes patient experience, clinical growth, and professional development. Clinical and Leadership Mentorship Program. Clinical Ladder for Advancement.

The Department of Neurology in the Division of General Neurology at Columbia University Vagelos College of Physicians and Surgeons is seeking an Associate Clinical Neurologist. Maintain a consistent level of excellence in clinical care and ensure adherence to best practices in patient management. Ac

Clinical Research Financial Specialist. This hybrid position manages the cash flow of a clinical study account from date of activation to date of closure; collects funds based on patient activity; manages payables as internal charges are incurred; assists grant managers with the application of funds

The Clinical Research Coordinator will support research activities within the Division of Nephrology at CUIMC. The incumbent will collect biospecimens-including kidney biopsy tissue-and clinical data from medical records, schedule and conduct follow-up visits, and ensure accurate data entry into res

Associate Director, Rare Hematology, Us Patient Advocacy. The Associate Director, Rare Hematology, US Patient Advocacy collaborates with relevant malignant and non-malignant Hematology and focused rare patient communities to understand unmet needs that inform business strategy, mobilize and empower

Experienced teammates are encouraged to become certified clinical instructors and mentor students. Assistant Clinical Director -Physical Therapist. Commitment to Clinical Excellence:.

Responsible for ensuring planning and direction of Clinical Pharmacology components of clinical programs (including clinical development plan/life cycle plan) and studies (including synopsis and protocol preparation; clinical phase oversight, reporting). Stays abreast of literature, government guide

IQVIA is seeking an experienced Associate Clinical Project Management Director/Trial Delivery Manager (TDM) to lead and coordinate global and regional clinical trial management activities. Associate Clinical Project Management Director/Trial Delivery Manager (TDM). IQVIA is a leading global provider

Oversees all current clinical research projects in the Interstitial Lung Disease Program, within Columbia University Irving Medical Center's Division of Pulmonary, Allergy & Critical Care. Facilitate and helps lead research team meetings. Assist with short term projects and provides cross coverage t