Jobs in the United States

25+ jobs

Save this search

Added just now
HU
Program Coordinator & Faculty Assistant (Part-time)
Harvard University
Cambridge, MA
- Part-time
Upload content to the Canvas learning platform and help design a pleasant student interface
Added 4 mins ago
Engineer – Internal Logistics Innovation & Projects
TKY Toyota Motor Mfg Kentucky, Inc Company
Georgetown, KY
New-model introduction which includes layout development, parts list & packaging confirmation, dolly design, automated deliveries, and conveyance equipment installations
Added 5 mins ago
Senior Electrical Engineer
Devens
Devens, MA
…well as adjacent industries such as semiconductor fabrication, data centers, utilities, advanced manufacturing, energy, and engineering or construction services. Direct GMP experience is…
Added 7 mins ago
Sr Software Engineer (Product Engineering Background)
Jobgether
Remote, United States
Join a fast-growing technology company transforming how businesses exchange data across global supply chains through modern, AI-powered infrastructure. As a Senior Software Engineer, you…
Added 7 mins ago
Senior Product Management Director
Jobgether
Remote, United States
…product managers and collaborate closely with engineering, design, marketing, sales, and customer success leadership. A key focus will be integrating advanced AI technologies into product…
Added 7 mins ago
J
Manager, Paid Media and Acquisition
Jobgether
Remote, United States
- $90,000 to $102,000 USD / year
…product, ecommerce, analytics, and franchise teams, you’ll turn data into measurable business results. The role offers significant autonomy, hands-on execution, and the opportunity to shape…
Added 7 mins ago
Sr Consultant, Software Engineering - Forward Deployed Engineering
Nationwide Life and Annuity Insurance Co
OH · AZ · IA
The Senior Consultant, Software Engineering (Forward Deployed Engineering) leads the design, development, deployment, and continuous improvement of complex AI solutions that address…
Added 7 mins ago
Consultant, Software Engineer - Platform Engineering
Nationwide Life and Annuity Insurance Co
OH · AZ · IA
The Consultant, Software Engineering supports the design, development, operation, and continuous improvement of reusable enterprise AI platforms and services that help teams deliver trusted…
Added 7 mins ago
Consultant, Software Engineer - Forward Deployed Engineering
Nationwide Life and Annuity Insurance Co
OH · AZ · IA
…HoneyHive, evaluation and observability tooling, guardrails, and developer…
Added 7 mins ago
Strategic Pricing Lead, TA
BP Products N.A. Inc.
Remote, United States
…pricing, sales, operations, supply, trading, finance, technology, data and analytics, while building team capability and representing TA in wider pricing…
Added 15 mins ago
Actuarial Analyst
Humana
Dover, DE
…forecasting solutions. This role will play a key part in the design and development of a holistic modeling solution, building new methodologies and frameworks from the ground up to support…
Added 15 mins ago
Lead Product Owner - Edge
Lumen
Dover, DE
Lumen is the trusted network for the AI‑powered world, connecting people, data, and applications through our expansive fiber network and connected ecosystem. We enable secure,…
Added 15 mins ago
Lead Product Manager, Next Best Action Use Case Management
Humana
Dover, DE
…integrated healthcare services, innovative technology, and data-driven…
Added 15 mins ago
Lead Product Manager, Value realization
Humana
Dover, DE
…integrated healthcare services, innovative technology, and data-driven…
Added 15 mins ago
Software Test Engineer
WCG Clinical
Dover, DE
Review requirements and design documentation to help ensure requirements are clear, testable, and consistent with the clinical trial protocol and system design specifications before test…
Added 16 mins ago
Build Engineer
Etched
San Jose, CA
Etched is building hardware for frontier intelligence. We co-design chips, racks, software, and manufacturing to deliver best-in-class throughput and latency across both prefill and decode…
Added 18 mins ago
SC
Scheduling Analyst
Solano Community College
Fairfield, CA
- $4,906.78 USD / month
Data entry of the college schedule of classes
Added 18 mins ago
Bus Experience & Planning Advisor - Retail Bank Operations
PNC Bank NA
United States
Accuracy and Attention to Detail, Analytical Thinking, Business Process Design, Data Gathering and Analysis, Effective Communications, Influencing, Planning: Tactical, Strategic, Problem…
Added 19 mins ago
Production Data & Process Support Specialist
(1137) Protein Sciences Corp
Pearl River, NY
Design and deliver training programs for manufacturing personnel on proper SAP transaction execution, iShift data entry protocols, and related digital workflows
Added 29 mins ago
Fishery Biologist 2- Chinook Monitoring Plan
Pacific States Marine Fisheries Commission
La Grange, CA
Plan, design, schedule, and conduct fish catch and effort surveys for marine fisheries. Utilize existing general creel survey protocols and determine modifications that address specific…
Added 34 mins ago
Staff Engineer - Developer Productivity
Jobgether
Remote, United States
As a Staff Engineer specializing in Developer Productivity, you will shape the engineering experience and technical infrastructure that enables a growing organization to build, test, and…
Added 34 mins ago
Staff Analytics Engineer
Jobgether
Remote, United States
Design, develop, and maintain scalable ELT/ETL pipelines using dbt, Airflow, SQL, and modern cloud-based data technologies.
Added 34 mins ago
Senior Security Consultant
Jobgether
Remote, United States
Design and recommend security architectures, technical controls, and improvement roadmaps aligned with SOC 2, ISO 27001, and HIPAA requirements.
Added 34 mins ago
Senior GRC Consultant
Jobgether
Remote, United States
Design, implement, and maintain comprehensive GRC programs, including security policies, control frameworks, risk management processes, and evidence management procedures.
Added 34 mins ago
Senior Full Stack Engineer
Jobgether
Remote, United States
…designing, developing, and scaling a sophisticated customer data platform that helps businesses seamlessly connect their data warehouses with everyday business tools. You will contribute…

Actalent

Clinical Research Associate

Pennington, NJ, United States

$130,000 USD / year

Apply About employer

Applications open in a new tab.

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.

Apply About employer

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

Report this job