Actalent logo

Clinical Study Manager

Actalent

Bernards, NJRemoteContract$85–95/hrTracked todaySeen in employer's feed today

Most applications go out cold — see where you stand first. Free, no sign-up to start.

At a glance

Compensation
$85–95/hr
Location
Bernards, NJRemote
Schedule
Contract
Work Authorization
Not specified

Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Actalent is hiring a Clinical Study Manager. The Clinical Study Manager delivers and executes global clinical studies, reporting to senior leadership while managing study start‑up, CROs, vendors, and regulatory responsibilities across multiple regions, ensuring quality, compliance, and operational efficiency.

Key focus areas include Provide leadership for a large‑scale global clinical trial across the U.S., Europe, and Asia‑Pacific regions, Manage critical study start‑up activities including central laboratory specifications, regulatory package review, site activation support, and cross‑functional study execution, and Oversee and manage CROs and third‑party vendors.

Important skills include Clinical Trial Management, Global Phase I Study Management, Global Phase II Study Management, Oncology Expertise, Vendor Oversight, and EU Clinical Trials Regulation Knowledge. Preferred (not required): Lung Oncology Expertise.

Skills & qualifications

RequiredNice to have

Skills

Clinical Trial ManagementGlobal Phase I Study ManagementGlobal Phase II Study ManagementOncology ExpertiseLung Oncology ExpertiseVendor OversightEU Clinical Trials Regulation KnowledgeIndependent OperationCollaboration SkillsCommunicationOral CommunicationFast-Paced Adaptability

Qualifications

8+ Years Clinical Trial Management ExperienceBachelor of Science DegreeExperience Leading Phase II or III Global StudiesPrior Experience Japanese CompanyClinical Research Associate ExperienceMust Be in Eastern Time Zone or Local to NJ/PA/NY

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match
Life Insurance
HSA/FSA
Paid Time Off
Sick Leave

Full job description

Job Title: Study ManagerJob Description

The Clinical Study Manager plays a pivotal role in delivering and executing global clinical studies under the guidance of a Study Delivery Lead. This role emphasizes tactical study delivery and involves reporting to a Director or a higher-level position. It requires excellent communication, project management skills, and meticulous attention to detail. The Clinical Study Manager interacts routinely with key internal and external stakeholders to convey project status, resolve issues, and address routine inquiries. This role may also involve responsibilities related to both operational strategy and study execution.

Responsibilities

  • Provide leadership for a large-scale global clinical trial across the U.S., Europe, and Asia-Pacific regions.

  • Manage critical study start-up activities, including central laboratory specifications, regulatory package review, site activation support, and cross-functional study execution.

  • Oversee and manage CROs and third-party vendors.

  • Handle EU Clinical Trials Regulation (EU CTR) responsibilities.

  • Collaborate with global stakeholders across multiple time zones.

  • Drive study milestones while ensuring quality, compliance, and operational efficiency.

Essential Skills

  • 8+ years of clinical trial management experience.

  • Strong experience managing global Phase I and/or Phase II studies.

  • Oncology background required; lung oncology experience is highly preferred.

  • Demonstrated experience overseeing vendors and leading complex, multi-country studies across the U.S., EU, and APAC regions.

  • Familiarity with EU Clinical Trials Regulation (EU CTR).

  • Ability to operate independently with minimal training.

Additional Skills & Qualifications

  • Bachelor of Science degree required.

  • Experience in clinical operations leading Phase II or III global studies.

  • Prior experience working for a Japanese company is a plus.

  • Experience as a Clinical Research Associate (CRA) is a plus.

  • Ability to adapt quickly to a fast-paced environment.

  • Strong collaboration skills.

  • Excellent written and oral communication skills.

Work Environment

The position is 100% remote but candidates must be in the Eastern Time Zone or local to the NJ/PA/NY area. Flexibility for face-to-face meetings is desired.

Job Type & Location

This is a Contract to Hire position based out of Basking Ridge, NJ.

Pay and Benefits

The pay range for this position is $85.00 - $95.00/hr.

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 Aug 25, 2026.

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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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 process due to a disability, please email [email protected] for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

You've read the whole posting — now see how you match it.