Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Clinical Study Manager

$85 - $95 per hour

Actalent

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 View email address on click.appcast.io 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.

Vacancy posted 5 days ago
Similar jobs that could be interesting for youBased on the Clinical Study Manager in Basking Ridge, NJ vacancy
  •  ...cost.Job Description1. Support individual clinical trial teams (CTTs) and Biomarker Sub-...  ...liaising with internal stakeholders. Assist Study Lead by forecasting the biosample...  ...analysis, and assisting with the relevant data management components. 4. With support, provide... 
    Suggested
    Work at office
    Immediate start

    Artech

    East Hanover, NJ
    4 days ago
  • $201.84k - $302.76k

     ...protocols, informed consent forms, and clinical sections of key submission documents. Oversees...  ...plans.Owns the development of study design to meet study objectives.Responsible...  ...Clinical Pharmacology (TMCP).With Data Management, co-leads the Integrated Data Review Plan... 
    Suggested

    Daiichi Sankyo

    Basking Ridge, NJ
    5 days ago
  •  ...Responsible for operational aspects of one or more clinical trials (phase I-IV, Expanded Access,...  ...external focus• Contributes to or manage simple clinical trial with minimal supervision...  ...Novartis Trials - provide feedback on study proposals, review submitted study concepts... 
    Suggested
    Contract work
    Work at office
    Local area
    Immediate start

    Artech

    East Hanover, NJ
    1 day ago
  •  ...Responsible for performing the ongoing review of clinical trial data as outlined in the data...  ...trila duration in collaboration with management.Collaborate with Medical Lead/BSL to identify...  ...and publishing global clinical studies in a pharmaceutical company or contract... 
    Suggested
    Contract work
    Work experience placement
    Work at office
    Immediate start

    Artech

    East Hanover, NJ
    4 days ago
  •  ...testing -Develop and maintain project- specific Data Management plan throughout the life-cycle of the study protocol, which includes CRF annotation, database...  ...evaluate efficiency, accuracy, and speed in cleaning clinical study data and locking database for study reporting... 
    Suggested
    Interim role
    Immediate start

    Artech

    Bridgewater, NJ
    4 days ago
  • $162.4k - $243.6k

     ...society.Job SummaryUnder supervision of Clinical Science Asset Lead or Clinical Science Lead...  ...minimal supervision to provide critical study-level support to the CSL/PS/MM/GCL for...  ...Clinical Pharmacology (TMCP).With Data Management, co-leads or provides input to the Integrated... 
    Work at office

    Daiichi Sankyo

    Basking Ridge, NJ
    5 days ago
  • $170k - $190k

    The Senior Clinical Trial Drug Supply Manager is a critical position within the clinical development organization directly supporting the execution...  ...submissions. This role will be responsible for multiple global studies and the independent oversight of drug supply forecasting... 
    Temporary work
    Work at office
    Flexible hours

    Amneal Pharmaceuticals

    Bridgewater, NJ
    3 days ago
  • $242.7k - $404.5k

     ...society.Job SummaryThe Senior Director, Clinical Safety Science is a key leadership role...  ...leadership for safety surveillance and risk management for a group of assets. Lead scientist...  ...leading safety scientist teams in clinical studies, regulatory submissions, aggregate... 

    Daiichi Sankyo

    Basking Ridge, NJ
    1 day ago
  • $90k - $130k

     ...Everest Clinical Research (“Everest”) is a full-service contract research organization (...  ...strong foundation as a statistical and data management center of excellence. Building on this...  ...tracking and reporting. Assist with study-level resource planning and management,... 
    Contract work
    Temporary work
    Work at office
    Remote work
    Work from home
    Worldwide

    Everest Clinical Research

    Bridgewater, NJ
    1 day ago
  •  ...Novartis seeks a Clinical Study Data Lead in East Hanover, NJ, with a hybrid model requiring 12 onsite days monthly. You will drive end-...  ...trial teams and stakeholders. Expect 5–8 years in clinical data management with deep knowledge of GCP, data standards, and regulatory... 

    Healthcare Businesswomen's Association

    East Hanover, NJ
    3 days ago
  • $165.5k - $214.17k

     ...lives of patients for generations to come. Clinical Operations is responsible for the...  ...commercialization of Gilead’s products. You will manage a team of direct and potentially indirect...  ...for the successful execution of studies and/or multiple studies within a program... 
    Contract work
    For contractors
    Local area
    Worldwide

    Kite Pharma

    Parsippany, NJ
    3 days ago
  •  ...contingent labor as a variable cost. Job Description The Clinical Program Manager will work cross functionally to develop, track and maintain...  ...programming) Please note: The manager is not looking for a study manager or a CRA/CTA. The candidate will not be working on... 
    For contractors
    Work at office
    Immediate start

    Artech Information System LLC

    Madison, NJ
    3 days ago
  • $164k - $282.9k

     ...Senior Medical Director Multiple Myeloma will be a member of the Global Medical Affairs team, leading the conduct of a global clinical study using the portfolio of compounds at J&J with the aim of building curative regimens for patients with multiple myeloma. The Senior... 
    Full time
    Temporary work
    Work experience placement
    Local area
    Remote work
    Worldwide

    Johnson & Johnson

    Raritan, NJ
    3 days ago
  • $196k - $342.7k

     ...merit. Job Function: Discovery & Pre-Clinical/Clinical Development Job Sub Function:...  ...Surgery. Leads a team responsible for clinical study design and delivery, outcomes research,...  ...Wound Closure & Healing business. Co-manage relationships with external scientific... 
    Full time
    Local area
    Immediate start

    Johnson & Johnson Innovative Medicine

    Raritan, NJ
    2 days ago
  •  ...DescriptionThis role is key for medical supervision and medical management of clinical trials proposed or to be performed by the Clinical Science & Operations Platform (CSO) of Sanofi R&D. The Clinical Study Director (CSD) is the medical reference in the clinical study... 
    Work at office
    Local area
    Immediate start

    Artech

    Bridgewater, NJ
    1 day ago
  •  ...Clinical Manager Responsible for all operational aspects of 1 or more OGD clinical trial(s) under the leadership of Clinical Trial Head (CTH). Support all scientific aspects of clinical trial(s) as assigned. Responsible for program level activities as assigned. Ensure... 
    Contract work
    Local area

    Integrated Resources

    East Hanover, NJ
    6 days ago
  • $237.4k - $298.9k

     ...Description Summary: The Senior Director, Clinical Pharmacology is responsible for...  ...also responsible for providing project management support for select projects in clinical...  ...delivery of all relevant clinical pharmacology studies. The incumbent works cross-functionally... 
    Contract work
    Temporary work
    Work experience placement
    Work at office

    PTC Therapeutics

    Warren, NJ
    1 day ago
  • $93.1k - $285.5k

    Job Summary:We are looking for Senior Project Leaders/Clinical Program Managers to join our innovative and dynamic group of global professionals...  ...best-in-class technology and data analytics. This role owns study and or program level timelines and planning;Microsoft... 
    Full time
    Part time
    Immediate start
    Worldwide

    IQVIA

    Parsippany, NJ
    4 days ago
  • $280.35k

     ...hopeful future for patients, their families, and society.Job SummaryThe Sr. Director, Clinical Safety, will lead the development and implementation of integrated project/product risk management strategies aimed at achieving the optimum benefit-risk for Development Sankyo's... 

    Daiichi Sankyo

    Basking Ridge, NJ
    4 days ago
  •  ...health-care professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value);...  ...content of protocols, Investigator Brochures, Clinical Study Reports, and Regulatory Submissions and responses. # Has overall... 
    Temporary work
    Local area
    3 days per week

    Allergan

    Florham Park, NJ
    1 day ago
  • $280.35k

     ...Senior Director sits within Global Oncology Clinical Development, an organization dedicated...  ...for one or more clinical trialsMatrix management responsibilities across the internal and...  ...external networkManages Phase 1 - Phase 3 studies (depending on assignment) with... 

    Daiichi Sankyo

    Basking Ridge, NJ
    3 days ago
  • $211k - $400.5k

     ...planning, execution, and interpretation of clinical trials or research activities of one or...  ...business strategy. Responsibilities: Manages the design and implementation of one or...  ...project-related education of investigators, study site personnel, and AbbVie study staff.... 
    Full time
    Local area

    AbbVie

    Florham Park, NJ
    4 days ago
  • $232k - $401.35k

     ...their merit.Job Function: Discovery & Pre-Clinical/Clinical DevelopmentJob Sub Function:...  ...development plans (including life-cycle management, geographic expansion, and post-marketing...  ...development, quality execution of clinical studies, preparation and ownership of clinical... 
    Full time
    Local area

    Johnson & Johnson

    Raritan, NJ
    3 days ago
  • $168.1k - $268.7k

     ...successful product launches and lifecycle management. Your work will influence key department...  ...to cross-functional teams, including Clinical Development, Regulatory Affairs, Commercial...  ...input into clinical development plans, study protocols, and operational documents to... 
    Hourly pay
    Worldwide

    Biontech

    Berkeley Heights, NJ
    more than 2 months ago
  • $210.38k - $272.25k

     ...together. Job Description Director, Clinical Operations – Oncology We are seeking a...  ...and will oversee the execution of complex studies, multiple studies within a program, or multiple programs. You will also manage assigned program resources, lead Clinical Operations... 
    Full time
    For contractors
    Local area
    Worldwide

    Gilead Sciences

    Parsippany, NJ
    3 days ago
  •  ...offering contingent labor as a variable cost.Job DescriptionResponsible for providing timely and prefessional ongoing quality management of clinical trial data by identifying errors/inconsistencies in CRF data and ensuring their resolutions in order that databases can be... 
    Local area
    Immediate start

    Artech

    East Hanover, NJ
    3 days ago
  •  ...serves as a valued strategic partner with Clinical, Commercial, Regulatory, and Market...  ...Medical Directors, Medical Science Liaison Managers, and Medical Science Liaisons) by cultivating...  ...execution of US Phase IIIB‑IV clinical study programs. Support the review and approval... 

    Sanofi

    Convent Station, NJ
    2 days ago
  • $117k - $201.25k

     ...Medicine is currently searching for the best talent for a Field Clinical Manager, Interventional Oncology in North America. This is a field-...  ..., our local teams, and multiple functions within our global study teams. Your primary responsibility will be to ensure that clinical... 
    Full time
    Local area
    Immediate start
    Remote work

    Johnson & Johnson

    Raritan, NJ
    3 days ago
  •  ...Executive Medical Director of Neurology, Clinical Development holds the responsibility to...  ...programs, including monitoring of clinical studies, review and interpretation of clinical...  ..., DMC charters, or other specific management plans and manuals in a cross-functional... 

    Katalyst Healthcares & Life Sciences

    Bridgewater, NJ
    2 days ago
  •  ...Clinical Data Manager Provide timely and professional ongoing management of Data Management deliverables and of clinical trial data with respect to cost, quality and timelines for assigned trials managed within Clinical Data Management. Ensure consistently high quality... 

    Integrated Resources

    East Hanover, NJ
    5 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Clinical Study Manager. Be the first to apply!