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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.

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

As a Senior Equity Research Associate, the successful candidate will work closely with an analyst in support of providing insights and research on numerous companies across the Building Materials spectrum. Senior Equity Research Associate. Within this, we are currently searching for a senior associa

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

Jefferies is seeking an equity research senior associate to support the Gaming, Lodging & Leisure team. Gaming, Lodging & Leisure Senior Associate. The senior analyst has covered the sectors for 18+ years.

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. Assist with the maintenance of clinical archive and electronic files.

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

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. Initiate studies performing initiation site visits, arrange for shipment

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.

An ideal candidate for our Clinical Project Associate position is an individual who can prioritize and multitask, is experienced in windows-based computer applications, and possesses strong communication skills. Job Description: Provide project management and operational support to designated clinic

Queens Hospital was recognized at ASCOs plenary session for their research efforts in enrolling patients in a diverse community and we welcome candidates who are interested in being an investigator in clinical trials for cooperative group studies, pharmaceutical studies and/or physician-initiated st

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

Interest in academic research and clinical trials related to gastrointestinal and liver diseases. Key Responsibilities: Examine, analyze, and interpret biopsies, resections, and other tissue samples related to the gastrointestinal tract, liver, pancreas, and associated structures. Provide accurate,

This leadership role offers a unique opportunity to shape the clinical, educational, and programmatic direction of our resident-based outpatient practice while building a specialty-focused gynecology career within a dynamic, university-affiliated community hospital. Provide clinical leadership and o

Board certification in combined Anatomic and Clinical Pathology, or in Anatomic Pathology.

The Associate Clinical Dermatologist (Pediatrics) will exhibit sustained excellence in clinical. Pediatrics) or a seasoned physician as Associate Clinical Dermatologist (Pediatrics). Associate Clinical Dermatologist Position.

Required Qualifications For Clinical Service Director (RN). Clinical Service Director (RN). Daily Responsibilities For Clinical Service Director (RN).

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. The DCE develops and supports the organization in clinical analysis, education, training, and strategic planning to drive clinical excellence. Completes a root cause analysis in focus center(s), regions, te

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

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

A minimum of 3 years' experience in Medical Device clinical trials, pharmaceutical, biotechnology or related firm, including direct exposure to the process of clinical study supply (IUO and Ancillary) management and execution. Collaborate with the Clinical Study team to include Medical Affairs, Clin

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.

The Clinic Director at SportsCare Physical Therapy is responsible for overseeing the day-to-day operations of the clinic, ensuring high-quality patient care, and managing the clinical and administrative staff. Supervise and mentor clinical staff, ensuring they adhere to best practices and provide qu

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

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.

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

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

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.

Stays abreast of literature, government guidelines, internal guidance on clinical trial conduct including Good Clinical Practice and internal SOPs, regulations for specific projects to which assigned, in order to be a team resource of clinical pharmacology and therapeutics knowledge in terms of both

Our Clinic Directors oversee all aspects of the clinic operations, manage clinical and non-clinical staff, and work with patients to provide individualized treatment and plans of care. Commitment to Clinical Excellence:. Experienced teammates are encouraged to become certified clinical instructors a

Admera Health is a genomic and bioinformatics research services company supporting pharmaceutical and biotech clients from early discoveries through clinical research. Title Level Commensurate with Experience (Senior Associate Scientist II or Scientist I). Experience in research-focused or biopharma

In collaboration with appropriate Clinical Trial Team (CTT) members: Ensure clinical support of trials as needed; conduct ongoing medical and scientific review of clinical trial data with Clinical Scientific Expert(s) with appropriate oversight from Medical Lead; manage patient safety reports on tri

Proven track record of leading innovation across the full lifecycle in pharmaceutical, consumer healthcare, and retail sectorsspanning consumer insights, product performance analysis, innovation planning, product development (pre-clinical/clinical), regulatory launch, and post-market monitoring. Ass

Admera Health is a genomic and bioinformatics research services company supporting pharmaceutical and biotech clients from early discoveries through clinical research. Title Level Commensurate with Experience (Senior Associate Scientist II or Scientist I). Experience in research-focused or biopharma

Attend company-wide meetings to discuss various company initiatives to continuously improve clinical excellence and patient care. With our continued expansion, we are able to offer tremendous growth opportunities for our clinical staff. Opportunity to mentor students as a Clinical Instructor.

A multi-specialty practice in Orange County is currently seeking an Oncologist for a promising opportunity with their growing team.Monday to Friday, 40 hours/week.Diagnose and treat various types of cancer in patients.Develop personalized treatment plans based on individual patient factors such as c

The Clinical Systems Analyst supports the implementation, maintenance, and optimization of clinical and administrative systems. Provide EMR (Athena) training for physicians, residents, and clinical/non-clinical staff. Act as a liaison between IT, clinical departments, and software vendors to communi

Manager, Senior Manager, or Associate Director). Exceptional communication and presentation abilities, with experience influencing senior executives. The Associate Director, Commercial Analytics, will serve as a key client-facing leader within KMK's Commercial Analytics Center of Expertise.

The Manager of Clinical Research Center Operations is responsible for Clinical Research Center Staff and other clinical support staff for all areas of Clinical Research across the Hackensack Meridian Health (HMH) network, ensuring compliance of all research studies and regulations. Manages Clinical

Our Clinic Directors oversee all aspects of the clinic operations, manage clinical and non-clinical staff, and work with patients to provide individualized treatment and plans of care. Commitment to Clinical Excellence:. Experienced teammates are encouraged to become certified clinical instructors a