Senior Clinical Study Manager

Lensa; New York (NY); Remote; Full time

Job summary

A leading career site seeks a Senior Clinical Study Manager to ensure the execution of clinical studies by overseeing CRO selection, managing study budgets, and ensuring adherence to standards. This fully remote position requires over 7 years of experience in clinical trials, particularly within oncology.

Benefits

Medical, dental & vision benefits

401(k) Retirement Plan

Short and long-term disability

Transportation benefits

Employee Assistance Program

Paid Time Off and Sick Leave

Qualifications

• 7+ years of experience as a GLOBAL Clinical Trial Manager in pharmaceuticals or biotech.
• Experience leading Phase II or III global studies within oncology.
• 5+ years of global experience within oncology (SOLID TUMORS) preferred.

Responsibilities

• Lead the development of clinical study plans and ensure compliance with quality measures.
• Monitor clinical trial performance, quality metrics, and manage study budgets.
• Coordinate study-related meetings and training sessions for team members.

Skills

Project Management

Stakeholder Communication

Clinical Trials Monitoring

Education

Bachelor of Science degree or higher

Job description

1 week ago Be among the first 25 applicants

Lensa is the leading career site for job seekers at every stage of their career. Our client, Actalent, is seeking professionals in New York, NY. Apply via Lensa today!

Job Title: Senior Clinical Study Manager

The Senior Clinical Study Manager is responsible for ensuring the successful execution and delivery of clinical studies across various geographic regions, adhering to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), FDA regulations, EU Directives, and ICH guidelines. This role requires extensive interaction with internal and external stakeholders to communicate project status, address issues, and provide expert-level guidance. The position reports to an Associate Director and involves both strategic planning and operational execution of clinical studies.

Responsibilities

• Lead the development of clinical study plans, identifying critical path activities and interdependencies.
• Create and manage the Clinical Study Oversight Plan, ensuring adherence and documentation of activities by CROs and vendors.
• Provide operational input into study protocols and amendments, and lead document review and coordination.
• Oversee CRO and vendor selection, scope of work creation, and ensure compliance with quality measures and timelines.
• Monitor clinical trial performance and quality metrics, escalating issues and proposing solutions as necessary.
• Ensure study adherence to internal procedures for planning, conduct, close out, and reporting.
• Monitor and reconcile study budgets, reviewing vendor invoices and ensuring alignment with Finance.
• Coordinate study-related meetings and training sessions, including vendor kick-off and investigator meetings.
• Support department in codifying knowledge and best practices, and prepare training materials.
  
  

Additional Skills & Qualifications

• 7+ years of experience as a GLOBAL Clinical Trial Manager with a pharmaceutical or biotech company.
• 5+ years of global experience within oncology (SOLID TUMORS!)
• Bachelor of Science degree or higher.
• Experience leading Phase II or III global studies within oncology
• Experience working for a Japanese company is a plus.
  
  

Work Environment

The team consists of a team lead and three study managers, with responsibilities in vendor management and regional assignments. The team operates in either the EU or US-Latin America regions, managing timelines, budgets, site activation, and enrollment. The role requires experience in study management, global experience, and overseeing CROs for study management activities.

Pay and Benefits

The pay range for this position is $90.00 - $98.00/hr.

Requirements

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
  
  

Workplace Type

This is a fully remote position.

Application Deadline

This position is anticipated to close on Jun 2, 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 [e-mail] ([e-mail]) for other accommodation options.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  IT Services and IT Consulting

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