Clinical trial jobs in New York, NY - Page 2Create job alerts

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000...

Through the practice of professional nursing the Oncology Clinical Research Nurse (RN) I prioritizes and advocates for the best interest of the patient enrolled on an oncology clinical trial while maintaining the fidelity of the clinical research protocol and compliance with policies, procedures ...

Job Title: Clinical Research Coordinator Job Description The Clinical Research Coordinator is responsible for coordinating the initiation and activation of all new clinical trial protocols. Review patients' charts and medical history with the Research Nurse Clinician (RNC) and/or physician t

Oversee the execution and delivery of a portfolio of GCO-supported clinical studies from the vendor management perspective across a specific therapeutic area, defining a Trial Vendor Management community. Manage resource allocation and collaborates with Vendor Program Strategy Directors to ensure...

From new trial modes to faster and integrated evidence and findings, our innovative clinical trial solutions mean we can unlock better evidence. Clinical Trial Endpoint Technology Solutions. Clario is a 50+ year old company that delivers industry-leading clinical trial endpoint technology solutio...

Job Description "Urgently Hiring!! Looking to fill as soon as possible!!” Job Summary QSAC is hiring for our Baldwin Day Habilitation program! We are looking for committed and energetic Behavior Intervention Specialists (BIS) who will conduct, assess and develop behavior support plans, addres...

Job Description "Urgently Hiring!! Looking to fill as soon as possible!!” Job Summary QSAC is hiring for our Day Habilitation program! We are looking for committed and energetic Behavior Intervention Specialists (BIS) who will conduct, assess and develop behavior support plans, address challe...

Job Description "Urgently Hiring!! Looking to fill as soon as possible!!” The salary range for this position is $52,000-$60,000 annually Behavior Intervention Specialists - Position Job Summary QSAC is hiring Behavior Intervention Specialists (BIS) across QSAC Program! We are looking for...

Job Description "Urgently Hiring!! Looking to fill as soon as possible!!” Job Summary QSAC is hiring for our Day Habilitation program! We are looking for committed and energetic Behavior Intervention Specialists (BIS) who will conduct, assess and develop behavior support plans, address challe...

Job Description "Urgently Hiring!! Looking to fill as soon as possible!!” Job Summary QSAC is hiring for our Residential Program! We are looking for committed and energetic Behavior Intervention Specialists (BIS) who will conduct, assess and develop behavior support plans, address challenges ...

Job Description "Urgently Hiring!! Looking to fill as soon as possible!!” Job Summary QSAC is hiring for our Day Habilitation program! We are looking for committed and energetic Behavior Intervention Specialists (BIS) who will conduct, assess and develop behavior support plans, address challe...

Job Description "Urgently Hiring!! Looking to fill as soon as possible!!” Job Summary QSAC is hiring for our Day Habilitation program! We are looking for committed and energetic Behavior Intervention Specialists (BIS) who will conduct, assess and develop behavior support plans, address challe...

Job Description "Urgently Hiring!! Looking to fill as soon as possible!!” Job Summary QSAC is hiring for our Day Habilitation program! We are looking for committed and energetic Behavior Intervention Specialists (BIS) who will conduct, assess and develop behavior support plans, address challe...

Job Description "Urgently Hiring!! Looking to fill as soon as possible!!” Job Summary QSAC is hiring for our Day Habilitation program! We are looking for committed and energetic Behavior Intervention Specialists (BIS) who will conduct, assess and develop behavior support plans, address challe...

Job Description "Urgently Hiring!! Looking to fill as soon as possible!!” Job Summary QSAC is hiring for our Day Habilitation program! We are looking for committed and energetic Behavior Intervention Specialists (BIS) who will conduct, assess and develop behavior support plans, address challe...

Job DescriptionDescription: About the company Shengsheng Supply Chain Management is an international logistics company that provides professional and integrated solutions for global time and temperature-sensitive cargo transportation. Professionally serving the life science, biotechnology and ph...

ROLE SUMMARY The Issue Support Associate (ISA) is an essential part of the Investigation Team and is responsible for supporting key investigation tasks for assigned Quality Issues to ensure compliance with timelines Good Clinical Practice (GCP) and Pfizer SOPs. The role collaborates with global...

May be assigned to lead clinical trial(s) as Clinical Scientific Lead and provide leadership and guidance for all clinical aspects of a clinical trial. As the medical/clinical lead interacts with and represents Novartis to global key opinion leaders and experts and may lead or co-chair steering c...

Position Summary** • Serves as a primary source of medical accountability and oversight for multiple clinical trials • Matrix management responsibilities across the internal and external network • Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities

Clinical Trial Manager** Responsibilities + Leads or collaborates on required tasks prior to commencement of senior clinical trials that include, but are not limited to: clinical planning, protocol development, case report form (CRF) development, IRB submissions, investigator agreements, info...

The Director of Clinical Trial Management is responsible for leading and overseeing the clinical monitoring aspects of clinical trials from study design through closeout. The Director will manage a team of Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) and will collaborate...

Driving execution of the section of the clinical program in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates, if applicable. The Clinical Development Director (CDD) in the Cardio Renal & Metabolic (CRM) Development Unit is res...

Responsibilities: Develop SAS programs and statistical output for the management and reporting of clinical trial data managed by GCD.Guarantee quality of statistical output produced by external provider, to program tools to support data review activities and data visualization, to collaborate on ...

Skills: coordinator, oncology, RN, research, clinical, OCN, "oncology certified nurse", clinical research Top Skills Details: coordinator, oncology, RN, research, clinical, OCN, "oncology certified nurse", clinical research Additional Skills & Qualifications: Must Haves: - IA

Serve as primary Operations contact for internal and external study team members/vendors on assigned studies and as the escalation point for vendors, investigators, and sites Contribute to the RFP process with a focus on operations-related vendors and study activities in collaboration with the P

Routinely perform and record physical inventory of a small clinical trial inventory area. Maintain Study Product and Study Supply inventory using Inventory management database. Inventory experience preferred.

Clinical Data Management Leadership.Provide clinical data management leadership within the study team to align on and drive data collection requirements for one or more complex clinical development projects.Efficiently plan, coordinate, and deliver complete, high quality and reliable clinical tri...

Actively participates in internal Trial Supply Management and Clinical Supply Chain meetings, Study Team meetings, Clinical Supply Matrix Team meetings and any other relevant meetings providing all relevant data and documentation prior to each meeting, highlighting any risks and mitigation strate...

Primary Responsibilities:** + Chair the Clinical Supply Program Team and works closely with Clinical Trial Teams (CTT), Project Management (PM), Regulatory, and other functional area representatives to negotiate timelines and strategy for clinical supplies + Acts as the main spokesperson between ...

As a Head of Product at EVYD Technology US, you will lead the strategy, development, and execution of our next-generation AI-powered clinical trial optimization platform. This is a high-impact leadership role where you will shape the future of AI in clinical development, working closely with AI e...

Position Summary / Objective** + Serves as a primary source of medical accountability and oversight for multiple clinical trials + Matrix management responsibilities across the internal and external network + Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabili

Serves as Clinical Trial Lead for one or more trials + Successfully leads, plans, and executes trial level activities for multiple trials with minimal to moderate level of supervision + Provides scientific and clinical leadership to team of supporting Clinical Scientists (matrix leadership)

Responsibilities: We are seeking a skilled Clinical Data Management Lead to oversee the execution of clinical trials.This role will be responsible for ensuring high-quality data collection, review, and delivery within scope, on time, and with precision.Lead clinical trial project teams, attending...

Clinical Development, Clinical Trial Planning, Dermatology, Dermatology Research, Launch Strategy, Market Access, Medical Affairs, Medical Dermatology, Medical Research, Pharmaceutical Medical Affairs, Pipeline Strategy, Project Management, Scientific Engagement, Strategic Thinking. Global Direct...

Job Description Title: Patient Care Technician (PCT), IP Unit - PRN Location: Staten Island About us: ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with expertise in early and late-stage neuroscience drug ...

Ensure lessons learned are communicated across teams and ensure alignment so that unnecessary amendments are avoided and to align with asset/TA-level protocol elements + May serve as Trial Lead for complex clinical studies + May present data/information to internal and external stakeholders

In partnership with Clinical Study Management, provide guidance and daily oversight for the successful in-house management of all aspects of international clinical trials, delivering high quality study data, on time and on budget. We are seeking a talented, experienced, and highly motivated Clini...

Clinical Trial Disclosure Senior Specialist.Role is 100% onsite CW can work from Madison, NJ or Lawrenceville, NJ Position Summary: The Clinical Trial Disclosure Senior Specialist will provide the operational support of:.Redaction of clinical trial documents in accordance with evolving global reg...

Responsibilities: Serve as lead CDM on assigned clinical trials by attending internal and external clinical trial project team meetings.Responsible for the study-specific data management tasks from protocol review to database lock to ensure data are collected, reviewed, and delivered with high qu...

Safety Reports) + Ensure collation and distribution of study tools and documents + Update clinical trial databases (CTMS) and trackers + Clinical supply & non-clinical supply management, in collaboration with other country roles + Manage Labeling requirements and coordinate/sign tran

This position provides legal oversight for the negotiation and management of clinical trial agreements, grant-funded research contracts, and collaboration agreements with academic and industry partners. Demonstrated ability to manage complex agreements and collaborate effectively with operational...

Job Description Oncology Clinical Pharmacy Specialist – Northern New Jersey (On-Site) Where Precision Meets Purpose: Transform Lives Through Clinical Research Are You Ready to Make an Impact? Do you excel at interpreting complex treatment protocols and translating them into safe, effective med...

As a Clinical Development Medical Director in Cardiovascular Renal & Metabolic, you will be responsible for the scientific and clinical strategy of assigned clinical trials, scientific monitoring, and reporting of quality data. Need thorough knowledge of Good Clinical Practice, clinical trial des...

Apply now and secure your spot in our next research study while positions are still available!. Join Our Part-Time Research Studies Today!. Are you eager to earn extra income from the comfort of your home? We are looking for motivated individuals to participate in paid research studies including ...

Are you eager to earn extra income from the comfort of your home? We are looking for motivated individuals to participate in paid research studies including focus groups, clinical trials, online surveys, secret shopping, and product reviews. Participate in focus groups, clinical trials, or online...

Are you eager to earn extra income from the comfort of your home? We are looking for motivated individuals to participate in paid research studies including focus groups, clinical trials, online surveys, secret shopping, and product reviews. Participate in focus groups, clinical trials, or online...

Are you eager to earn extra income from the comfort of your home? We are looking for motivated individuals to participate in paid research studies including focus groups, clinical trials, online surveys, secret shopping, and product reviews. Join Our Part-Time Research Studies Today!. This is an ...

Join Our Part-Time Research Studies Today!. Are you eager to earn extra income from the comfort of your home? We are looking for motivated individuals to participate in paid research studies including focus groups, clinical trials, online surveys, secret shopping, and product reviews. This is an ...