Top 31 Clinical study manager Jobs in Armonk, Ny

Manager, Clinical Study Lead
Regeneron —Armonk, NY
- $128,600 - $210,000 a year
- Microsoft Word
- Microsoft Excel
- 6 years
- Health insurance
- Dental insurance
Clinical Study Associate Manager
Regeneron —Armonk, NY
- $109,900 - $179,300 a year
- Bachelor's degree
- Travel
- Mentoring
- Health insurance
- Dental insurance
Senior Clinical Study Manager (Hybrid)
Stryker —Mahwah, NJ
- $132,100 - $220,100 a year
- Full-time
- Hybrid work
- Bachelor's degree
- Agile
- Senior level
- Health savings account
- AD&D insurance
10d
Manager, Clinical Programming (Remote)
Penfield Search Partners —Fairfield, CT
- Contract
- Remote
- Computer Science
- Bachelor's degree
- Organizational skills
Quick Apply
Technical Clinical Data Manager /Data Analyst (Remote)
Penfield Search Partners —Fairfield, CT
- Contract
- Remote
- 5 years
- Bachelor of Science
- SQL
Quick Apply
1d
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
Part -Time Clinical Research Coordinator
Optum —Mount Kisco, NY
- $24 - $43 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
- AD&D insurance
- Employee stock purchase plan
3d
Manager, Precision Medicine Operations
Regeneron —Armonk, NY
- $114,800 - $187,400 a year
- 5 years
- Bachelor's degree
- Team management
- Health insurance
- Dental insurance
Manager, Clinical Imaging Operations
Regeneron —Tarrytown, NY
- $128,600 - $210,000 a year
- Management
- 5 years
- Bachelor of Science
- Health insurance
- Dental insurance
Clinical Trials Manager-B
Stamford Health —Stamford, CT
- Full-time
- 5 years
- Computer literacy
- Office
- Free parking
- Health insurance
Quick Apply
3d
Research Project Manager
New York State Psychiatry Institute —New York, NY
- $80,698 - $82,000 a year
- Full-time
- Adults
- Mid-level
- University
Quick Apply
Program Manager Clinical Research
Montefiore Einstein —Bronx, NY
- $84,000 - $105,000 a year
- Full-time
- Mid-level
- 3 years
- Master'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
Research Scientist 4
State of New York - People With Developmental Disabilities, Office for —Orangeburg, NY
- $106,898 - $135,665 a year
- Full-time
- Background check
- Master's degree
- Bachelor's degree
- Free parking
- Paid parental leave
10d
Associate Director, Clinical Research
NS Pharma Inc —Paramus, NJ
- $175,000 - $205,000 a year
- 8 years
- Bachelor's degree
- Contracts
- Health savings account
- AD&D insurance
Quick Apply
3d
Administrator II - IRB
Nathan S. Kline Institute —Orangeburg, NY
- $78,285 - $94,392 a year
- Full-time
- Bachelor of Science
- Mid-level
- Analysis skills
Quick Apply
3d
Director, Clinical Research
NS Pharma —Paramus, NJ
- $210,000 - $245,000 a year
- Full-time
- Hybrid work
- Office
- Bachelor's degree
- Travel
- Health savings account
- AD&D insurance
Physician - In Patient Mental Health Manager
US Veterans Health Administration —Montrose, NY
- $290,000 - $315,000 a year
- Online Application
- Background check
- Medicine
- Surgery
- Paid holidays
- Loan repayment program
Data Coordinator I
Columbia University —Fort Lee, NJ
- $66,300 - $68,000 a year
- Full-time
- Hybrid work
- Computer literacy
- HIPAA
- Office
Director, Clinical Research
NS Pharma Inc —Paramus, NJ
- $210,000 - $245,000 a year
- Full-time
- Hybrid work
- Office
- Bachelor's degree
- Travel
- Health savings account
- AD&D insurance
Quick Apply

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Manager, Clinical Study Lead

Regeneron -
Armonk, NY

Apply Now

Job Details

$128,600 - $210,000 a year

Benefits

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

Qualifications

Microsoft Word
Clinical program budget management
Staff supervision
Fiscal management
Microsoft Excel
Clinical study protocols and reports
Presentation software
Research project design
Team development
ICH guidelines
IVR
Bachelor's degree
Managing clinical research teams
Vendor relationship management
Leading team collaboration initiatives
Vendor contract management
Research regulatory compliance
Clinical quality assurance standards
Microsoft Project
Research and development project management
Cross-functional team management
Technical Proficiency
Cross-functional communication
Operational budget management

Full Job Description

Build our future together:

The Manager, Clinical Study Lead may perform the following responsibilities with moderate oversight: accountable for the global execution of assigned smaller or less complex clinical trials from study design, through execution, to study close out. You are accountable for the study timelines, study budget, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies outsourced to Clinical Research Organizations (CROs) and the balance of direct leadership versus oversight will vary accordingly. Contributes and drives ongoing process improvement initiatives.

When & where:

Work Location: Armonk, NY, Warren, NJ
25% Travel may be required

Discover your role:

Leads the cross-functional study team responsible for clinical study delivery, serving as the primary point of contact for leadership and oversight, and oversees execution against planned timelines, deliverables, and budget while raising issues (conduct, quality, timelines, budget) to the Program Operations Lead and stakeholders and implementing corrective actions
Provides operational input into protocol development; leads feasibility assessments to select relevant regions and countries; oversees or conducts site evaluation and selection; and leads investigator meeting preparation and execution
Oversees and contributes to study documentation, including case report forms, data management plan, monitoring plan, monitoring oversight plan, project-specific training plan, data review plan, statistical analysis plan, and related materials
Oversees set-up and maintenance of study systems (e.g., CTMS, TMF) and ensures compliance with clinical trial registry requirements
Identifies outsourcing needs and leads vendor engagement, contracting, and management; ensures CROs and third-party vendors are aligned and delivering per scope of work
Provides input into baseline budget and timeline development and management; ensures accurate budget management and scope change control for internal and external studies
Leads study-level risk assessment and mitigation; monitors site activation and monitoring visits and acts on deviations; leads development and oversees implementation of patient recruitment and retention strategies and responds to deviations from plan; and monitors data entry and query resolution against agreed metrics
Manages study close-out activities, including database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability; contributes to clinical study report writing and review; and facilitates study-level lessons learned
Assigns tasks to Clinical Study Management staff and supports their deliverables; directly supervises CTM staff (work assignments, performance management, recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight); recommends and participates in cross-functional and departmental process improvements; and identifies innovative, globally informed approaches to study execution and continuous improvement of CTM SOPs
May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring

This role requires:

Bachelor’s degree and have at least six years of relevant industry experience
Extensive budget management expertise; a proven ability to build productive study teams and collaborations; and demonstrated vendor management experience
Strong technical proficiency with trial management systems and Microsoft applications is required, including Project, PowerPoint, Word, Excel, and platforms such as IVRS/IWRS and EDC
Experience in global clinical trial operations, including developing protocols and key study documents; solid knowledge of ICH/GCP and relevant regulatory guidelines and directives; and effective project management, cross-functional team leadership, and organizational skills
Ability to understand and implement the operational strategic direction and guidance for respective clinical studies

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)

$128,600.00 - $210,000.00

Apply Now

Refine Your Search

clinical study manager jobs in armonk, ny

Manager, Clinical Study Lead

Clinical Study Associate Manager

Senior Clinical Study Manager (Hybrid)

Manager, Clinical Programming (Remote)

Technical Clinical Data Manager /Data Analyst (Remote)

Senior Manager, Clinical Study Inspection Readiness

Part -Time Clinical Research Coordinator

Manager, Precision Medicine Operations

Manager, Clinical Imaging Operations

Clinical Trials Manager-B

Research Project Manager

Program Manager Clinical Research

Clinical Research Coordinator I

Research Scientist 4

Associate Director, Clinical Research

Administrator II - IRB

Director, Clinical Research

Physician - In Patient Mental Health Manager

Data Coordinator I

Director, Clinical Research

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