Jobs in the United States

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Added 1 min ago
3rd Grade Teacher (INR)
Academy District 20
Colorado Springs, CO
Establishes and communicates high expectations and use processes to support the development of critical-thinking and problem-solving skills
Added 3 mins ago
Senior Mission Operations Engineer
Blue Origin Personnel, LLC
Reston, VA · Denver, CO
…operations engineers in accomplishing these tasks throughout the program lifecycle, while also collaborating extensively with engineers from across the space and ground segments. The ideal…
Added 3 mins ago
CO
Administrative Support I
City of Dublin
Dublin, OH
- $20.38 to $29.9 USD / hour
The City of Dublin is currently accepting applications for an Administrative Support I role. This position serves as the first point of contact for residents at our City Hall location,…
Added 3 mins ago
IT Audit, Cybersecurity & Risk Senior Consultant (Financial Services Focus)
Baker Tilly Advisory Group, LP
United States
You feel valued when you are provided the resources and support to continually sharpen your technical skills and build your career now, for tomorrow
Added 4 mins ago
Test Equipment Engineer
Nissan North America, Inc. (NNA)
Farmington Hills, MI
…teams, laboratory operations personnel, equipment suppliers, and management to ensure equipment solutions meet technical requirements, budget objectives, and operational needs. In addition…
Added 9 mins ago
TX Operations Volunteer
The A21 Campaign
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Provide on-site support at the Freedom Center to accommodate flexible case management scheduling
Added 9 mins ago
NC Operations Volunteer
The A21 Campaign
Charlotte, NC
Provide on-site support at the Freedom Center to accommodate flexible case management scheduling
Added 10 mins ago
Shift Manager
Buffalo Wild Wings
Arden, NC
…restaurant on a shift-by-shift basis. You will also assist the management team in providing support and coaching team members to ensure tasks are performed effectively, helping create…
Added 12 mins ago
SB
Executive Assistant to the President
SUNY Brockport NY
Brockport, NY
- $85,000 to $95,000 USD / year
…President provides high-level executive and administrative support to the President and ensures efficient daily operations of the Office of the President. The Executive Assistant manages…
Added 13 mins ago
Senior Account Executive, GTS
Gartner
Arlington, VA
Account management with an outcome of increased customer satisfaction and an increase in retention and account growth
Added 15 mins ago
SH
Home Health Physical Therapist
Supplemental Health Care
Ludlow, MA
- $1,478 to $1,629 USD / week
Provide skilled interventions for strengthening, endurance, pain management, and fall prevention
Added 15 mins ago
Cardiac Catherization Cath Lab Technologist - Albany, New York
Supplemental Health Care
Albany, NY
…Hospitals nationwide with competitive pay, benefits, and dedicated…
Added 15 mins ago
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Case Management Registered Nurse
Supplemental Health Care
Mattoon, IL
- $2,062 to $2,243 USD / week
Supplemental Health Care is connecting Case Management Registered Nurses with top-tier hospital contracts in Mattoon, Illinois.
Added 15 mins ago
SH
Home Health Physical Therapist
Supplemental Health Care
Bourne, MA
- $2,028 to $2,253 USD / week
Provide skilled interventions for strengthening, endurance, pain management, and fall prevention
Added 15 mins ago
Cardiac Catherization Cath Lab Technologist - Brandon, Florida
Supplemental Health Care
Brandon, FL
…Hospitals nationwide with competitive pay, benefits, and dedicated…
Added 15 mins ago
Catheterization Laboratory Tech Cath Lab Technologist - Sun City Center, Florida
Supplemental Health Care
Sun City Center, FL
…Hospitals nationwide with competitive pay, benefits, and dedicated…
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Clinical Manager - RN - Home Health
Supplemental Health Care
Silverdale, WA
- $2,232 to $2,419 USD / week
Responsible for Referral Intake and Management to ensure that clients receive assessment visits and that these visits are scheduled and performed timely
Added 15 mins ago
Cardiac Cath, Cath Lab/CVIV Cath Lab Technologist - Albany, New York
Supplemental Health Care
Albany, NY
…Hospitals nationwide with competitive pay, benefits, and dedicated…
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Paraprofessional | Walled Lake, Michigan
Supplemental Health Care
Walled Lake, MI
- $21.25 to $22.9 USD / hour
Do you have a heart for helping others and a passion for education? Are you patient, flexible, and ready to support students in a meaningful way? Supplemental Healthcare is hiring…
Added 15 mins ago
SH
Home Health Physical Therapist
Supplemental Health Care
Franklinton, NC
- $2,210 to $2,381 USD / week
Provide skilled interventions for strengthening, endurance, pain management, and fall prevention
Added 15 mins ago
SH
Clinical Manager - RN - Home Health
Supplemental Health Care
Lake Oswego, OR
- $2,230 to $2,489 USD / week
Responsible for Referral Intake and Management to ensure that clients receive assessment visits and that these visits are scheduled and performed timely
Added 15 mins ago
SH
Home Health Physical Therapist
Supplemental Health Care
Aberdeen, WA
- $2,016 to $2,239 USD / week
Provide skilled interventions for strengthening, endurance, pain management, and fall prevention
Added 15 mins ago
SH
Home Health Physical Therapist
Supplemental Health Care
Anmoore, WV
- $2,784 to $2,965 USD / week
Provide skilled interventions for strengthening, endurance, pain management, and fall prevention
Added 15 mins ago
SH
Home Health Physical Therapist
Supplemental Health Care
Easton, MD
- $2,044 to $2,260 USD / week
Provide skilled interventions for strengthening, endurance, pain management, and fall prevention
Added 16 mins ago
Coordinator for Academic Programs
Harvard University
Cambridge, MA
Provides comprehensive administrative support to the Associate Dean for Academic Programs, including calendar management, meeting coordination, travel arrangements, preparation of briefing…

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 EnvironmentThe 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 & LocationThis is a Permanent position based out of Pennington, NJ. Pay and BenefitsThe 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 & LocationThis is a Permanent position based out of Pennington, NJ. Application DeadlineThis position is anticipated to close on Nov 6, 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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More about this job

Skills

Clinical research
Clinical trials
Regulatory compliance
Google Cloud
Monitor activities
Reporting
Documentation
Inspection
Communication skills
Presentation skills
Research
Collaboration
Interpersonal skills
EDC
Microsoft Office
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Microsoft Outlook
Problem solving
Time management
Financial management

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