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Retail Sales Manager
Harbor Freight Tools
Mobile, AL
- $25.5 to $28.5 USD / hour
186543BRJob Description: Our Assistant manager (full-time) is a valued member of a high performing team who is empowered & equipped to do their job. You will know why your work matters and…
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Corporate Security General Associate Manager
Wells Fargo
BIRMINGHAM, AL
Knowledge and understanding of Access Control, CCTV, and Alarm, Systems operations. (Lenel On-Gard, March Networks, Biometrics)
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Senior Director, Plant Manager – Missile Integration & Electronics
Leidos
Huntsville, AL
The Plant Manager is responsible for the overall leadership, performance, and operational effectiveness of a manufacturing facility supporting missile integration and test operations and…
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Sr Manager - Proj/Prog
Maximus
Montgomery, AL
The Sr. Manager provides overall leadership and management for assigned federal contact center programs and serves as the primary management focal point responsible for the administrative,…
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Pharmacy Technician Refill Authorization
Intermountain Health
Montgomery, AL
Any lapse or failure to meet these requirements may result in disciplinary action, up to termination, at the hiring manager's discretion.
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Buyer I or II
Intermountain Health
Montgomery, AL
Develops close working relationship with aligned category manager(s) to identify and implement cost, quality, and supply continuity improvements.
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Product Manager - Technical
Intermountain Health
Montgomery, AL
The Technical Product Manager is responsible for driving the development and management of technology-driven products and solutions that support our health plan operations. Collaborates…
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Sales and Service Technician
Bridgestone Americas
Montgomery, AL
Bridgestone Retail Operations (BSRO) is part of Bridgestone Americas and employs over 22,000 teammates in North America. BSRO operates more than 2,200 company-owned stores, including…
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Pharmacy Technician Specialty Pharmacy
Intermountain Health
Montgomery, AL
Any lapse or failure to meet these requirements may result in disciplinary action, up to termination, at the hiring manager's discretion.
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Facets Product Consultant - Manager
Cognizant
Montgomery, AL
- $113,000 to $130,000 USD / year
Strong understanding of healthcare payer operations and end-to-end health plan business processes.
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Regulatory Readiness Program Manager
Meta
Montgomery, AL
Regulatory Readiness Program Manager Responsibilities:
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Regional Maintenance Manager
CBRE
Montgomery, AL
- $200,000 to $210,000 USD / year
…looking for a skilled and forward-thinking Regional Maintenance Manager (RMM) to join our growing team as we work to service one of the world’s largest online…
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Pharmacy Technician Central Fulfillment
Intermountain Health
Montgomery, AL
Any lapse or failure to meet these requirements may result in disciplinary action, up to termination, at the hiring manager's discretion.
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Food Operations Manager 2
Sodexo
MONTGOMERY, AL
- $64,600 to $83,600 USD / year
Lead food operations for a new employee café and oversee multiple micro kitchens within a premier corporate services account. Drive guest satisfaction, team engagement, and operational…
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Principal Material Project Manager
Leidos
Huntsville, AL
The PMPM reports to the Material Operations & Strategies Associate Director, is directly aligned to the Program Manager, and represents Material Operations & Strategies on customer…
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Director of Export & Compliance - 1015
Quantinuum
Broomfield, CO
- $175,000 to $235,000 USD / year
- Oversee compliance program operational execution through the Compliance Project Manager, including training calendars, audit tracking, policy rollouts, and compliance reporting.
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Manufacturing Manager - 1107
Quantinuum
Broomfield, CO
- $162,000 to $218,000 USD / year
- Build effective partnerships with quality, supply chain, program management, operations, design engineering, and external suppliers to manage dependencies, resolve risks, and meet…
Added 5 mins ago
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Customer Service & E-Commerce Associate Team Leader (Customer Service, In-Store Shopper Assistant Department Manager)
Whole Foods Market
Atlanta, GA
- $20.05 to $35 USD / hour
…orders, excellent pickup experience, team productivity, and program execution. You will monitor key performance indicator metrics and visual cues in-store to assess the Team’s performance…
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E T Consultant Senior Health Specialist
World Bank Group
Washington, DC
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Financial Analyst - E2- Orlando, FL
Lockheed Martin
Orlando, FL · Orlando
You will be a Program Finance Analyst supporting the Geospatial portfolio for the Program Finance & Business Operations team. Our team is responsible for business management, program…
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Integrated Program Planning Asc Mgr - L4 - TX
Lockheed Martin
Arlington, TX · Arlington
Lockheed Martin’s Integrated Program Planning Team – Where Precision Meets Innovation!
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Multifunctional Manufacturing Supv - L3
Lockheed Martin
Troy, AL · Troy
You will be the Manufacturing Supervisor for our team in Troy, AL, reporting to the Program Manager. Our team is responsible for the day-to-day operations of a work group, ensuring…
Added 7 mins ago
Program Management Stf - E4
Lockheed Martin
Lexington, KY · Lexington
The Program Manager for Special Operations Forces Global Logistics Services (GLSS) will lead execution of maintenance and modification efforts in the Aviation Mission Area for H-60 series…
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Project Management & Planning Operations Rep Stf - E4
Lockheed Martin
Fort Worth, TX · Fort Worth
The Project Management & Planning Operations Representative will oversee the operational aspects of ongoing corrective actions responses for the F35 program. Serves as liaison between…
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Asst. Director, Marketing and Videoboard Operations
University of Miami
Coral Gables, FL
Assist the manager of Production Services with shows across other sports as needed

Actalent

Clinical Trial Manager

Lexington, MA, United States

$70 to $75 USD / hour

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Job details

Pay: $70 to $75 USD / hour
Posting language: English
Posted: Nov 3, 2026

Original job description

Job Title: Clinical Trial ManagerJob DescriptionThis role leads and oversees a high-priority global Phase III clinical trial in an ultra-rare disease with aggressive timelines. The Clinical Trial Manager provides sponsor-side operational leadership, ensuring effective CRO and vendor oversight, site management, timeline adherence, quality control, and inspection-ready documentation. The position offers significant visibility and ownership across global study operations and is intended to ramp up ahead of a key leadership transition to ensure continuity on this critical program.

Responsibilities

Lead the planning, implementation, execution, and oversight of a global Phase III clinical study in alignment with the protocol, budget, milestones, and regulatory requirements.
Serve as the primary sponsor contact for the contract research organization (CRO) and managed vendors, overseeing performance, KPIs, monitoring quality, and managing risks, issues, and escalations.
Provide strong sponsor-side operational leadership across CRO and vendor oversight, global sites, timelines, and trial quality.
Coordinate and lead cross-functional study team activities across Clinical Development, Data Management and Statistics, Regulatory, Safety, Drug Supply, Finance, and other key functions to ensure seamless execution.
Support new site identification and selection as enrollment expands, including in APAC and European regions, and ensure sites are activated and supported effectively.
Oversee Trial Master File (TMF) quality to maintain inspection readiness, including management of risk, issue, and decision logs and corrective and preventive action (CAPA) activities as needed.
Support the development and management of contracts and change orders, including vendor and site budgets, to ensure financial control and alignment with study needs.
Contribute to the review of clinical data to support data quality, consistency, and readiness for analysis and regulatory submission.
Oversee study supplies and logistics to ensure sites have the necessary materials and drug supply to support uninterrupted trial conduct.
Lead or support site and vendor closeout activities, ensuring proper documentation, data reconciliation, and regulatory compliance.
Operate effectively in a mid-study environment with tight timelines and evolving enrollment and site needs, proactively identifying and resolving operational challenges.
Maintain a strong focus on inspection readiness and compliance with ICH-GCP and applicable clinical research regulations throughout the study lifecycle.
Collaborate with global stakeholders and regional teams, including those in Europe and APAC, to ensure consistent execution and communication across regions.

Essential Skills

Proven ability to independently run or oversee a global clinical study, ideally at the Phase III stage.
Strong sponsor-side CRO and vendor oversight experience, including performance management, KPI tracking, and issue escalation.
Demonstrated ability to operate effectively in a mid-study environment with tight timelines and changing enrollment and site needs.
Strong knowledge of ICH-GCP and applicable clinical research regulations, with a particular focus on inspection readiness.
Demonstrated cross-functional leadership skills and the ability to collaborate effectively with global teams, including Europe and APAC.
Hands-on experience in clinical trial operations and vendor management.
Degree in biomedical, pharmaceutical, life sciences, or a related discipline; MSc preferred.
Target of 57 years of relevant clinical operations experience, specifically with meaningful Clinical Trial Manager experience; 35 years may be considered for a strong high-achiever capable of performing the role.
Sponsor-side experience strongly preferred; profiles with only CRO experience are not the primary target.
Experience leading global Phase III studies preferred.
Willingness to travel as required for study needs and stakeholder engagement.

Additional Skills & Qualifications

MSc in biomedical, pharmaceutical, life sciences, or a related field is preferred and considered an asset.
Global Phase III study leadership experience is highly desirable.
Rare disease clinical trial experience is a significant plus.
Biotech experience is a significant advantage, though strong candidates from large pharmaceutical environments may also be considered.
Proven ability to manage complex stakeholder relationships across CROs, vendors, and internal cross-functional teams.
Strong organizational, communication, and problem-solving skills, with a focus on proactive risk identification and mitigation.
Motivation to take on a highly visible leadership role in a critical global ultra-rare disease program, with potential for long-term continuity.
Interest in a career path that offers broad sponsor-side ownership across CRO and vendor oversight, global site management, TMF and inspection readiness, and cross-functional operations.

Work EnvironmentThis position is primarily remote, offering flexibility while maintaining strong collaboration with global teams. Candidates based in the Northeast are preferred, with the Massachusetts/Boston area considered a plus due to the ability to come into the office periodically for in-person meetings and collaboration. The role involves working with global stakeholders across multiple time zones, including Europe and APAC, which may occasionally require flexible hours to support cross-regional communication. The environment is fast-paced and execution-focused, centered on a high-stakes global Phase III ultra-rare disease program. The Clinical Trial Manager will work extensively with CROs, vendors, and internal cross-functional teams using standard clinical trial technologies and systems to manage timelines, TMF quality, inspection readiness, and study documentation. Travel may be required to attend key meetings, site visits, or vendor engagements, depending on study needs. Job Type & LocationThis is a Contract position based out of Lexington, MA. Pay and BenefitsThe pay range for this position is $70.00 - $75.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.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) Job Type & LocationThis is a Contract position based out of Lexington, MA. Application DeadlineThis position is anticipated to close on Nov 17, 2026. Workplace TypeThis is a fully remote position.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 actalentaccommodation@actalentservices.com 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.

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Skills

Research
Leadership
Data management
Statistics
Inspection
Financial jurisdiction
Logistics
Documentation
Regulatory compliance
Google Cloud
Clinical research
Communication skills
Performance management
Vendor management
Stakeholder management
Problem solving
Collaboration

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