Jobs in the United States

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Added 3 mins ago
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Operations Coordinator - Production
San Antonio Water System
San Antonio, TX
- $26.46 to $45.39 USD / hour
JOB SUMMARYThe Operations Coordinator will support and assist the Vice President - Production Operations in achieving goals for the department, which is operational excellence, readiness,…
Added 5 mins ago
Dean of Liberal Arts & Social Science
Central Wyoming College
RIVERTON, WY
…catalog material pertaining to divisional programs, coordinating program advisory committees, articulating programs within college and external colleges, universities and agencies,…
Added 5 mins ago
Licensing Coordinator
Ford Motor Company
Cheyenne, WY
Vehicle discount program for employees and family members and management leases
Added 5 mins ago
Facilities Coordinator
CBRE
Cheyenne, WY
…serving, valuations); Building Operations & Experience (facilities management, property management, flex space & experience); Project Management (program management, project management,…
Added 5 mins ago
Bookkeeper/Finance Coordinator
Converse County Aging Services
DOUGLAS, WY
…tracking. Working closely with the Finance Director, the Finance Coordinator helps maintain accurate financial records and responsible management of organizational and program…
Added 8 mins ago
BioLife Medical Support Specialist - LPN
USA - 3387 BioLife Plasma Services, LP
Towson, MD
…expected. You will determine donor eligibility to donate plasma, management of donor adverse events, review of laboratory test results, and donor notification of unsuitable test results.…
Added 9 mins ago
Operations Coordinator - Scottsdale, AZ
Tiffany
Scottsdale, AZ
The Operations Coordinator takes the lead by performing all back of house operations in a Tiffany store. The Coordinator has a passion for providing excellent client service and partners…
Added 25 mins ago
Guest Coordinator
Ulta Beauty, Inc.
Foley, AL
The Guest Coordinator is responsible for engaging with guests and promoting the Ulta Beauty services business through one-on-one guest interactions, both over the phone and in-person. They…
Added 30 mins ago
Materials & Equipment Coordinator
The Davey Tree Expert Company
Richfield, OH
The Materials & Equipment Administrator is an essential part of Davey Resource Group’s Utility Asset Management (UAM) material and equipment procurement process and is responsible for…
Added 32 mins ago
ENTERPRISE CONSENT GOVERNANCE LEADER-PRIVACY
Kroger Family of Companies
Cincinnati, OH
Serve as the business owner for Kroger's consent management platform(s), including Ketch, and lead platform administration, governance operations, implementation coordination, stakeholder…
Added 32 mins ago
Onsite Staffing Coordinator in Fairfield, OH!
Employment Solutions Management, Inc
Cincinnati, OH
Description STAFF PERFORMANCE COORDINATOR Fairfield, OH Job SummaryUnder direct supervision, the Staff Performance Coordinator contributes to the operational growth and profitability of the…
Added 50 mins ago
Manager, Program
University of Utah
Salt Lake City, UT
…Student & Scholar Services (ISSS) provides a continuum of case management for international student & scholar support cases including assessment, planning, collaboration, implementation,…
Added 1 hour ago
LI
Data Entry Clerk | M-F | $15/hr | 8am-5pm | Causal Dress!*
Larjar, Inc.
Tampa, FL
- $15 USD / hour
Other duties as assigned by Supervisor, Team Lead or member of management
Added 1 hour ago
UG
Heavy Equipment Operator / Landfill
Unified Government of Athens-Clarke County
Winterville, GA
- $40,721 USD / year
Continuation of this Recruitment/Hiring Incentive Program is subject to available funding and approval by the Manager.
Added 1 hour ago
UG
Program Support Analyst I
Unified Government of Athens-Clarke County
Athens, GA
- $49,497 USD / year
…financial records; assistance with tracking and maintaining agency program accomplishments; utilizing the Housing and Urban Development (HUD's) Integrated Disbursement and Information…
Added 1 hour ago
CH
Supportive Housing Coordinator
COMMUNITY HOUSING NETWORK INC
COLUMBUS, OH
- $24 to $27.52 USD / hour
As a Supportive Housing Coordinator, you will provide direct support to CHN’s Supportive Services operations by coordinating services, education, and community referrals that empower…
Added 1 hour ago
TC
AV Schools Resource Technician - PT
The Classical Academy
Colorado Springs, CO
- $19.22 USD / hour
Provides coordinated support and works closely with the Fine Arts Coordinator for all performing arts events.
Added 1 hour ago
SO
Administrative Coordinator 4
State of Louisiana
Shreveport, LA
- $15.76 to $27.01 USD / hour
The Administrative Coordinator-4 is an advanced administrative and specialized support position requiring extensive knowledge of the SSA Disability Program, the appellate process, and all…
Added 1 hour ago
Centralized Staffing Coordinator
Texas Children\'s
Houston, TX
We’re searching for a Centralized Staffing Coordinator, someone who works well in a fast-paced setting. In this position, you’ll be responsible for supporting hospital operations through…
Added 1 hour ago
CH
Project Coordinator (4076)
CHILDRENS HUNGER FUND
Sylmar, CA
- $20 to $26.26 USD / hour
The Project Coordinator will facilitate efficient department workflow and diligently ensure that department projects and initiatives that promote and elevate the visibility of Children’s…
Added 1 hour ago
Licensing Coordinator
Ford Motor Company
Phoenix, AZ
Vehicle discount program for employees and family members and management leases
Added 1 hour ago
DH
ECMO Program Coordinator
Dignity Health
Phoenix, AZ
- $45.26 to $67.32 USD / hour
You will oversee ECMO Program general operations in collaboration with ECMO Medical Staff Leadership including but not limited to program coordination quality monitoring education and…
Added 1 hour ago
MC
Kinesiologist (1-Year Limited Tenure)
Mayo Clinic
Phoenix, AZ
- $27.99 to $41.98 USD / hour
Contribute to data management and processing.
Added 1 hour ago
J
Director, Employee Relations
Jobgether
Remote, United States
- $155,000 to $175,000 USD / year
In this senior leadership role, you will oversee the Employee Relations function, establishing consistent standards for workplace investigations, case management, and employment practices.
Added 1 hour ago
Registered Nurse
Appalachian Regional Healthcare, Inc.
Beckley, WV
Reports up chain of command Clinical Nurse Manager/Nurse Manager/House Nurse Coordinator pertinent information

Actalent

Clinical Research Associate

Pennington, NJ, United States

$130,000 USD / year

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Job details

Pay: $130,000 USD / year
Experience: Minimum 5 years of onsite clinical monitoring experience, including experience with Phase III clinical trials.
Posting language: English
Posted: Oct 31, 2026

Original job description

Clinical Research Associate (Midwest-Based)

This role offers an experienced Clinical Research Associate the opportunity to move into a sponsor-side environment and play a central role in managing and monitoring Phase III clinical trials. You will oversee site-level clinical operations, ensure adherence to protocols and regulatory requirements, and work closely with cross-functional study teams to support the delivery of potentially life-changing therapies. The position is based in the Midwest and involves extensive travel to investigative sites, strong visibility within the clinical program, and meaningful ownership of site performance and study outcomes.

Responsibilities

Manage and monitor clinical trial activities at assigned study sites to ensure compliance with the protocol, Good Clinical Practice (GCP), and applicable regulatory requirements.
Serve as the primary point of contact for investigators and site staff, fostering strong and collaborative relationships.
Plan, conduct, and document all required site visits, including Site Qualification Visits (SQV), Site Initiation Visits (SIV), Interim Monitoring Visits (IMV), and Close-Out Visits (COV).
Perform comprehensive site management activities to ensure project timelines, milestones, and deliverables are met.
Leverage in-depth knowledge of the study protocol to safeguard subject safety, ensure protocol compliance, and protect the integrity and validity of study data.
Ensure all site management and monitoring activities are conducted in compliance with ICH-GCP, standard operating procedures (SOPs), the Clinical Monitoring Plan (CMP), study plans, and applicable local laws and regulations.
Verify the accuracy and completeness of study data through detailed source data review and source data verification (SDR/SDV).
Conduct initial and ongoing training and retraining of site staff on protocol requirements, study procedures, and study-specific tools as needed.
Manage site-level queries, protocol deviations, and operational issues, escalating concerns appropriately and in a timely manner.
Ensure investigative sites update clinical trial data systems accurately and within required timelines.
Oversee timely and accurate reporting of adverse events (AEs), serious adverse events (SAEs), and drug safety (DS) events, including appropriate follow-up to completion.
Prepare, submit, and maintain high-quality visit reports, follow-up letters, and related documentation within required timelines.
Maintain accurate, complete, and up-to-date study files, including regulatory documents and monitoring records.
Support and facilitate site audits and regulatory inspections by ensuring inspection readiness and addressing findings as needed.
Contribute to site feasibility assessments and support the development and execution of patient recruitment strategies.
Act as a liaison between investigative sites and the sponsor, ensuring effective communication, timely issue resolution, and alignment on study expectations.
Collaborate with sites to develop, adapt, and track subject recruitment plans that align with project needs and enhance enrollment predictability.
Attend project meetings and provide clear, concise updates on site status, enrollment progress, and key operational metrics.
Identify operational risks at the site level and recommend appropriate mitigation strategies.
Ensure safety events and other reportable occurrences are properly documented, followed, and closed to completion in collaboration with safety surveillance.
Lead and conduct presentations to internal teams, site personnel, and other stakeholders as needed.
Coordinate, organize, and manage clinical study coordinator teleconferences on a routine basis when required.
Collaborate with contract research organizations (CROs) and vendors to manage site-level activities and resolve operational challenges.
Contribute to patient recruitment and retention initiatives and support long-term site relationship management.
Operate effectively in a fast-paced, dynamic environment by proactively addressing issues, proposing solutions, and maintaining focus on study goals.

Essential Skills

Minimum 5 years of onsite clinical monitoring experience, including experience with Phase III clinical trials.
Demonstrated experience in a sponsor environment or working closely with sponsors on clinical programs.
Strong knowledge of and skill in applying clinical research regulatory requirements, including ICH-GCP guidelines.
Experience in site management, including planning and conducting SQV, SIV, IMV, and COV visits.
Proven ability to manage serious adverse events in collaboration with safety surveillance teams, ensuring events are followed through to completion.
Effective organizational, communication, and interpersonal skills, with the ability to build strong relationships with site personnel and internal stakeholders.
Ability to lead and conduct presentations for internal teams and site staff.
Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) platforms.
Proficiency with the Microsoft Office suite, including Word, Excel, PowerPoint, and Outlook.
Strong analytical and problem-solving abilities, with the capacity to identify risks and propose mitigation strategies.
Experience working in a fast-paced, collaborative environment with shifting priorities.
Effective time management and financial management skills to support efficient site operations.
Willingness and ability to travel up to 80%, including frequent overnight stays.
Bachelors degree in a scientific discipline or healthcare-related field (preferred).

Work Environment

The role is based in the Midwest and involves frequent travel to investigative sites, with up to approximately 80% travel including overnight stays. You will work in a smaller, performance-driven clinical-stage environment where individual contributions are highly visible and closely tied to the success of the clinical program. The culture emphasizes collaboration, innovation, and action, and is best suited for proactive, solutions-oriented professionals who are comfortable taking initiative rather than waiting for direction. Clinical Operations team members are expected to take strong ownership of their studies, manage challenges directly with CROs and vendors, and bring forward practical solutions.

Job Type & Location

This is a Permanent position based out of Pennington, NJ.

Pay and Benefits

The pay range for this position is $130000.00 - $130000.00/yr.

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.

Annual bonus: 1015% 401(k): 5% company match Tuition reimbursement: Up to $8,000/year Cell phone reimbursement: $125/month Paid time off: At least 10 vacation days + 5 sick days Paid holidays: 12/year Healthcare: Medical and dental coverage Additional: Employee rewards/recognition program Benefits should be confirmed for the specific FTE offer, as eligibility and plan details may vary.

Job Type & Location

This is a Permanent position based out of Pennington, NJ.

Application Deadline

This position is anticipated to close on Nov 6, 2026.

Workplace Type

This 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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