1,140 Results for

Clinical Research Associate Jobs in Chinatown, NY

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Clinical Research Coordinator (CRC) System One

Riverdale, NJ

$33 / hour
Quick Apply

We are looking for an experienced Clinical Research Coordinator to support day-to-day clinical trial operations at an onsite research site in Riverdale, NJ, with travel to nearby locations. This full-time contract-to-hire role requires independent coordination of participant visits and documentation while also performing blood draws, specimen processing, and injections (within the scope of clinical qualifications).

12 days ago

Associate Director, US Clinical Supply Business Management, GCSO Daiichi Sankyo, Inc.

Basking Ridge, NJ

$162,400–$243,600 / year
Full time

Additionally, the role will serve as a key member of the Global Clinical Supply Committee (GCSOC), providing the Project Management Office (PMO) support in organizing and facilitating Committee meetings and ensuring progress is achieved with other Committee members continuously. This role is accountable to the Head, Clinical Supply & Business Management - Global Clinical Supply Operations (GCSO) to drive the vision and implementation of the Business Management function in the US (DSI) through close collaboration with Global Business Management colleagues in Japan and Germany.

30+ days ago

Clinical Contracts Associate System One

Riverdale, NJ

Remote

$30–$35 / hour
Quick Apply

In this role, you will review, negotiation, and execution of Clinical Trial Agreements (CTAs) and related amendments, while partnering closely with internal teams and external sponsors/CROs. The ideal candidate is highly organized, comfortable working independently, and confident driving multiple priorities in a fast-moving clinical research environment.

4 days ago

Oncology CRA-Sponsor side! Jobot

New York, NY

$125,000–$140,000 / year
Quick Apply

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4 days ago

Quantitative Clinical Pharmacology PhD Fellow Daiichi Sankyo, Inc.

Basking Ridge, NJ

$100,960–$151,440 / year
Full time

Develop Model-Based Drug Development Plans (MBDD) and Clinical Pharmacology plans for early development candidates and work closely with QCP WG leads and non-clinical teams (non-clinical PK, translational science and pharmacology) to identify FIH dosing and early development plans. Daiichi Sankyo’s PhD Fellowship Program offers early-career scientists a unique opportunity to launch their careers at the forefront of drug development and innovation focusing on advancing model informed drug development.

3 days ago

Senior Director, Global Clinical Supply Quality Assurance Daiichi Sankyo, Inc.

Basking Ridge, NJ

$209,850–$349,750 / year
Full time

Strategic Leadership & Oversight and Cross-Functional Team Participation: Cross-Functional Team Participation: Develop, lead, participate or manage resources that support various working groups Responsible to contribute to the achievement of global QA vision and enhance globalization at DS QA-GMP affiliates, proactively support and contribute to the development and execution of regional and global QA GMP strategies, internal and external collaboration, activities and initiatives that support and drive compliance and improvement opportunities for IMP, new and established products; Ensure a strong interface with Pharmaceutical Technical Development, CSO, RACMC to ensure full QA visibility and proactive engagement of QA across stakeholder. Drug Product Release and Oversight of Clinical Trial Materials Lifecycle: Drug Product Release: Exercise leadership in order to execute a comprehensive drug product release program for commercial and investigational drug products and assures that all external contractors involved in manufacturing and testing provide GMP compliant release documentation ensuring satisfactory QA review and approval of drug product master production records.

10 days ago

Associate Director, Biostatistics (Late Stage Oncology) Daiichi Sankyo, Inc.

Basking Ridge, NJ

$175,440–$263,160 / year
Full time

Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies including study design, protocol development, CRF review, SAP development, analysis files development, statistical analysis accuracy validation, results interpretation and CSR input and review. Global BDO Strategy to Improve Drug Development: Primarily participates and may occasionally lead moderately complex initiatives, with some level of supervision, to improve the harmonization and efficiency of drug development which leads to cost savings and shortened timelines for the company.

30+ days ago

Associate Program Dir., IM Residency Physician Yale New Haven Health

Greenwich, CT

$165.75–$275.91 / hour

The individual must demonstrate knowledge of the principles of growth and development over the life span and possess the ability to assess data reflective of the patient's status and interpret the appropriate information needed to identify each patient's requirements relative to his or her age-specific needs, and to provide the care needed as described in the unit's/area's/department's policies and procedures. 1 Assist PD, APD's, CR and PA develop and oversee the allocation of residents in their various rotations in order to satisfy ACGME and Residency Review Committee requirements for successful completion of an internal medicine residency with particular attention to the overlap between outpatient and inpatient assignments.

5 days ago

Phlebotomist Kaygen Inc.

Franklin Lakes, NJ

$30–$38 / hour
Temporary
Contractor
Full time
Quick Apply

We specialize in providing high-volume contingent staffing, direct hire staffing and project-based solutions to companies worldwide ranging from startups to Fortune 500 and Managed Service Providers (MSP) across a wide variety of industries. The phlebotomist will recruit subjects for clinical studies and perform blood collections, prepare specimens for laboratory testing as well as perform screening procedures according to specific protocol procedure requirements.

2 days ago

Clinical Research Associate I - Center for Interventional Cardiovascular Research and Clinical Trials Mount Sinai Health System

New York, NY

$58,661–$81,675 / year

Mount 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.

30+ days ago

Clinical Research Associate - Sponsor Dedicated IQVIA

Parsippany, Kansas

In this role, you will be responsible for overseeing clinical trial sites to ensure studies are conducted in compliance with study protocols, regulatory requirements, Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, and sponsor expectations. Successful candidates will possess strong site management skills, a commitment to quality, and the ability to build productive relationships with investigators and site personnel.

25 days ago

Clinical Research Associate (CRA) Zp Group Llc

$110,000–$130,000 / year

Responsibilities: of the Clinical Research Associate include: · Perform remote monitoring and source data verification activities to ensure study data accuracy, completeness, and regulatory compliance. · Conduct site initiation visits (SIVs) and participate in onsite monitoring visits when required to support study milestones and quality objectives.

6 days ago

Sr. Clinical Research Associate/Clinical trial Manager BridgeBio Pharma Inc

$145,000–$177,000 / year

Lead operational management for assigned regions and sites by driving site initiation activities, monitoring performance metrics, identifying and mitigating risks, driving escalations and action-item closure, and representing regional performance in study team and cross-functional discussions. Lead aspects of vendor management for the CRO and other key vendors (IRT, imaging, central and specialty labs, etc.), establishing expectations, ensuring deliverables are met, performance measures are maintained, and escalating as needed; address performance gaps and drive corrective actions to closure.

30+ days ago

Senior Clinical Research Associate (Field- Based) - Multiple Openings NAMSA Inc

$68,800–$133,700 / year

Assess the suitability of potential investigative sites through screening interviews, regulatory document review and evaluation of study information and provides input to the site selection process. Supports study start-up activities such as tracking and performing quality review of study documents, completing, and distributing site activation letters, etc.

30+ days ago

Spec 2, Clinical Operations, Clinical Research Associate MillenniumSoft Inc

Franklin Lakes, NJ

Quick Apply

Maintains quality results by following study protocol procedures and testing schedule; recording all pertinent information required during processing procedures. Tracks collected specimens by initialing, dating, and noting times of collection; maintaining daily metrics of lab activities performed.

1 day ago

Clinical Research Associate II - FSP Precision Medicine Group LLC

$91,500–$137,300 / year

Precision's uniquely integrated offerings enable the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for complex disease states. Essential 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.

9 days ago

Clinical Research Associate - 170044 Zp Group Llc

$100,000–$140,000 / year

Partner with investigative sites and internal study teams to address findings, resolve issues, and maintain study timelines. Responsibilities: of the Clinical Research Associate (CRA): Conduct onsite and remote monitoring activities to evaluate study progress, participant safety, and protocol compliance.

30+ days ago

FSP Sr. Clinical Research Associate II - Northeast - Ophthalmology Fortrea Inc

Remote

$125,000–$142,000 / year

Responsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.

9 days ago

Senior Clinical Research Associate - 177466 Zp Group Llc

$155,000–$175,000 / year

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. Qualifications: for the Senior Clinical Research Associate include: · Minimum of 2+ years of oncology monitoring experience with current expectations of approximately 3 years of independent monitoring.

6 days ago

Clinical Research Associate National Veterinary Associates

Remote

$80,000–$95,000 / year

This role serves as a strategic and operational lead for assigned studies, exercising discretion and independent judgment in planning trial activities, identifying and resolving site and study issues, prioritizing competing demands, and driving decisions that materially influence study timelines, site performance, sponsor satisfaction, data quality, and overall business results. The CRA acts as a primary liaison among sponsors, hospital teams, and internal stakeholders and is expected to operate with a high degree of autonomy in managing study conduct, recommending solutions, setting priorities, and shaping processes that support the successful delivery of Ethos Science services.

13 days ago

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Clinical Research Associate Jobs in Chinatown, NY

Clinical Research Coordinator (CRC) System One

Associate Director, US Clinical Supply Business Management, GCSO Daiichi Sankyo, Inc.

Clinical Contracts Associate System One

Oncology CRA-Sponsor side! Jobot

Quantitative Clinical Pharmacology PhD Fellow Daiichi Sankyo, Inc.

Senior Director, Global Clinical Supply Quality Assurance Daiichi Sankyo, Inc.

Associate Director, Biostatistics (Late Stage Oncology) Daiichi Sankyo, Inc.

Associate Program Dir., IM Residency Physician Yale New Haven Health

Phlebotomist Kaygen Inc.

Clinical Research Associate I - Center for Interventional Cardiovascular Research and Clinical Trials Mount Sinai Health System

Clinical Research Associate - Sponsor Dedicated IQVIA

Clinical Research Associate (CRA) Zp Group Llc

Sr. Clinical Research Associate/Clinical trial Manager BridgeBio Pharma Inc

Senior Clinical Research Associate (Field- Based) - Multiple Openings NAMSA Inc

Spec 2, Clinical Operations, Clinical Research Associate MillenniumSoft Inc

Clinical Research Associate II - FSP Precision Medicine Group LLC

Clinical Research Associate - 170044 Zp Group Llc

FSP Sr. Clinical Research Associate II - Northeast - Ophthalmology Fortrea Inc

Senior Clinical Research Associate - 177466 Zp Group Llc

Clinical Research Associate National Veterinary Associates

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