Top 110 Clinical study manager Jobs in New York State

Clinical Study Associate Manager
Regeneron —Armonk, NY
- $109,900 - $179,300 a year
- Bachelor's degree
- Travel
- Mentoring
- Health insurance
- Dental insurance
Manager, Clinical Study Lead
Regeneron —Armonk, NY
- $128,600 - $210,000 a year
- Microsoft Word
- Microsoft Excel
- 6 years
- Health insurance
- Dental insurance
Assistant Director of Community Mental Health Services
Livingston County, NY —Geneseo, NY
- $80,000 - $82,000 a year
- Full-time
- Writing skills
- Licensed Clinical Social Worker
- Outpatient experience
Quick Apply
RN Pediatric Clinical Research - PRN
Professional Case Management —Plattsburgh, NY
- $60 an hour
- PRN
- CPR Certification
- Nursing
- Clean driving record
- On-the-job training
Quick Apply
Senior Manager, Clinical Study Inspection Readiness
Regeneron —Armonk, NY
- $150,500 - $245,500 a year
- Bachelor of Science
- 8 years
- Travel
- Health insurance
- Dental insurance
Clinical Project Manager - Oncology (Client Dedicated/Remote)
サイネオス・ヘルス —New York State
- $120,000 - $135,000 a year
- Remote
- Mid-level
- 3 years
- Bachelor's degree
- Employee stock purchase plan
- Health insurance
Associate Manager / Manager, Project Services - Laboratories (Remote - East Coast)
IQVIA —Ithaca, NY
- $64,200 - $173,000 a year
- Full-time
- Remote
- Microsoft Excel
- Computer literacy
- Data analysis skills
- Work from home
Manager, Clinical Research
University of Rochester —Rochester, NY
- $70,600 - $105,800 a year
- Full-time
- Office
- Master's degree
- University
7d
Program Implementation Manager, Clinical Studies
American Heart Association —New York, NY
- $70,000 - $90,000 a year
- Full-time
- Remote
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Wellness program
- Paid holidays
8d
Clinical Data Manager
Cardiovascular Research Foundation —New York, NY
- $80,000 - $110,000 a year
- Weekends as needed
- Hybrid work
- Writing skills
- Mid-level
- Office
- Paid holidays
- Disability insurance
Quick Apply
Assistant Clinical Research Manager
Columbia University —New York, NY
- $85,000 - $91,000 a year
- Full-time
- Hybrid work
- Mid-level
- University
- Bachelor's degree
Clinical Research Coordinator I
Columbia University —New York, NY
- $66,300 - $68,000 a year
- Full-time
- Hybrid work
- Spanish
- Customer service
- HIPAA
Senior Manager, Clinical Research
Butterfly Network —New York, NY
- $200,000 - $215,000 a year
- Hybrid work
- Nursing
- Office
- Bachelor's degree
- Health savings account
- Employee stock purchase plan
Quick Apply
Clinical Research Assistant
Adams Clinical —New York, NY
- $24.00 - $26.92 an hour
- Vital signs
- High school diploma or GED
- Bachelor's degree
- Health savings account
- Health insurance
Research Program Manager
NYU Langone Health —New York, NY
- $84,577.93 - $109,200.00 a year
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Wellness program
Clinical Research Site Manager, HBN
Child Mind Institute —New York, NY
- $76,500 - $95,000 a year
- Full-time
- Hybrid work
- Mid-level
- Office
- 3 years
- Paid parental leave
- Health insurance
Quick Apply
Senior Clinical Trial Manager
Katalyst Healthcares & Life Sciences —Manhattan, NY
- Contract
- Hybrid work
- Microsoft Outlook
- Computer literacy
- 3 years
Quick Apply
14d
Sr. Clinical Trials Project Manager
University of Rochester —Rochester, NY
- $70,600 - $105,800 a year
- Full-time
- Hybrid work
- 5 years
- Master's degree
- University
4d
Senior Clinical Research Manager - CICET
Columbia University —New York, NY
- $130,000 - $150,000 a year
- Full-time
- Spanish
- Nursing
- Microsoft Excel
Clinical Research Coordinator - Rheumatology
Columbia University —New York, NY
- $66,300 a year
- Full-time
- Spanish
- Customer service
- HIPAA

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Clinical Study Associate Manager

Regeneron -
Armonk, NY

Apply Now

Job Details

$109,900 - $179,300 a year

Benefits

Health insurance
Dental insurance
Paid time off
Vision insurance
401(k) matching

Qualifications

Clinical program budget management
Fiscal management
Presentation software
Project documentation
ICH guidelines
IVR
Bachelor's degree
Vendor relationship management
Vendor contract management
Clinical quality assurance standards
Microsoft Project
Achieving project delivery timelines
Medical terminology
Technical Proficiency
Operational budget management

Full Job Description

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Clinical Study Associate Manager to join our Clinical Trial management team. In this role, you will support the Clinical Study Lead by taking responsibility for areas of clinical trial delivery, applying to both internally sourced studies and studies out-sourced to CROs, while collaborating with the study team internally and externally with vendors such as CROs.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

Location: Armonk, NY, Warren, NJ
Hybrid: 4 days per week onsite
Travel percentage: May require 25% travel

Discover your role:

May lead/oversee the planning and management of a clinical study in an assigned region(s) in alignment with global study plans, and may contribute to global planning and management of the study
Contributes to risk assessment and helps identify risk mitigation strategies, and supports feasibility assessment to select relevant regions and countries
Oversees and provides input to the development of study specific documentation (e.g., CRF, data management plan, monitoring plan, monitoring oversight plan) and reviews site level informed consents and other patient-facing study start-up materials
Oversees setting up and maintenance of study systems including CTMS and TMF, and contributes to investigator meeting preparation and execution
Oversees engagement, contracting and management of required vendors for the study, and oversees and provides input to study drug and clinical supplies' forecasting, drug accountability and drug reconciliation
Provides regular status reports to collaborators as requested by the Clinical Study Lead, and contributes to development of and oversees implementation of recruitment and retention strategies
Monitors recruitment and retention, and monitors progress for site activation and monitoring visits
Supports data quality including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations and suspected non-compliance by sites, and escalates data flow and data quality issues to Clinical Study Lead
Oversees the execution of the specific clinical study deliverables against planned timelines, escalates issues related to timelines or budget to Clinical Study Lead, and supports accurate budget management and scope changes
Contributes to clinical project audit and inspection readiness throughout the study lifecycle, and supports internal and external inspection activities and contributes to CAPAs as required
Manages aspects of study close-out activities including database lock, reconciliation of vendor contract, study budget, TMF and study drug accountability, may mentor clinical trial management staff, and may be assigned unmasked tasks for studies (e.g., unmasked TMF management, unmasked data review, IVRS point of contact)

This role requires:

Bachelor's Degree and 4+ years of relevant industry experience
Excellent communication and interpersonal skills; ability to build relationships internally and externally
A data driven approach to executing and problem solving, and attention to details for the ability to deliver on specific study activities
Technical proficiency in trial management systems and MS applications including Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC, TMF
Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization
Budget awareness with the ability to participate in various aspects of budget management
Familiarity with medical terms, and vendor management experience
Experience in clinical trial operations including experience developing key study documents
Knowledge of ICH/GCP and regulatory guidelines/directives

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Salary Range (annually)

$109,900.00 - $179,300.00

Apply Now

Refine Your Search

clinical study manager jobs in new york state

Clinical Study Associate Manager

Manager, Clinical Study Lead

Assistant Director of Community Mental Health Services

RN Pediatric Clinical Research - PRN

Senior Manager, Clinical Study Inspection Readiness

Clinical Project Manager - Oncology (Client Dedicated/Remote)

Associate Manager / Manager, Project Services - Laboratories (Remote - East Coast)

Manager, Clinical Research

Program Implementation Manager, Clinical Studies

Clinical Data Manager

Assistant Clinical Research Manager

Clinical Research Coordinator I

Senior Manager, Clinical Research

Clinical Research Assistant

Research Program Manager

Clinical Research Site Manager, HBN

Senior Clinical Trial Manager

Sr. Clinical Trials Project Manager

Senior Clinical Research Manager - CICET

Clinical Research Coordinator - Rheumatology

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