Jobs in the United States

25+ jobs

Save this search

Added just now
Revenue Integrity Charge Auditor
Intermountain Health
Frankfort, KY
…regulatory information. Provide guidance with policy and procedure development, training and support, and applicable clinical education focused to reduce clinical…
Added just now
C
Business Analyst with Healthcare Experience
Cognizant
Frankfort, KY
- $83,000 to $94,500 USD / year
Collaborate closely with Product Management, Compliance, Operations, UX, Development, and QA teams to ensure successful delivery of business objectives.
Added just now
C
VMware & Windows Infrastructure Architect
Cognizant
Frankfort, KY
- $100,000 to $115,000 USD / year
…cloud engineering teams, infrastructure delivery teams, and operations teams to deliver secure, scalable, resilient, and cost-effective technology…
Added just now
Integrations Program Manager
Meta
Frankfort, KY
Meta is seeking an Integrations Program Manager to lead complex, cross-functional integration programs that connect Meta's products, platforms, and operations at scale. In this role, you…
Added just now
Application Analyst Willow Inpatient
Intermountain Health
Frankfort, KY
Gathers, validates, and translates technological requirements into design and development specification while providing product management
Added just now
Senior Analyst, Provider Compliance
CVS Health
Frankfort, KY
…strategies. Applies deep expertise in compliance, business operations, analytics, and communication to develop and execute strategies that support regulatory and contractual obligations.…
Added just now
UP
Apprentice Freight Car Repair - South Morrill, NE
Union Pacific
SO MORRILL, NE
- $33.7 USD / hour
Join our team at one of North America's leading railroad companies and embark on a comprehensive three-year training program to become a skilled Freight Car Repairer! As an apprentice in…
Added just now
Distribution Sourcing Analyst (Remote)
BAE Systems
Nashua, NH · Austin, TX · Ft. Wayne, IN · Cedar Rapids, IA
You will serve as a critical link between our program requirements and our global distribution partners. From managing high-value procurements to navigating complex market conditions, you…
Added just now
R
Senior Director, Technical Training
Reworld
Louisville, KY
- $7.25 USD / hour
…implementation of an organization-wide strategic technical training program. A significant component of this role will be to build a comprehensive structured on the job training program…
Added just now
AE
Summer Intern - Quality Engineer
Apogee Enterprises Inc
Louisville, KY
- $7.25 USD / hour
…for Summer 2027. These positions go from May-August (12-week program) and offer hands-on project experience, professional development, and much…
Added just now
US
Summer Intern - Quality Engineer
UW Solutions
Louisville, KY
- $7.25 USD / hour
…for Summer 2027. These positions go from May-August (12-week program) and offer hands-on project experience, professional development, and much…
Added just now
ES
Assistant Store Manager
Extra Space Storage
Louisville, KY
- $16 to $17 USD / hour
The Assistant Store Manager plays a pivotal role in supporting the daily operations of one or more self-storage locations, under the guidance of the District Manager and Store Manager. This…
Added just now
Seasonal Assistant District Manager
Jackson Hewitt - GUU
Chicago, IL
…business from the ground up providing real business leadership development and experience as well as deep understanding of critical components of business success (recruitment/retention…
Added just now
Seasonal Assistant District Manager
Jackson Hewitt - GUU
East Peoria, IL
…business from the ground up providing real business leadership development and experience as well as deep understanding of critical components of business success (recruitment/retention…
Added just now
Faculty – Surgery Administration, Research Focus (Open Rank, Tenure-Track)
The Ohio State University
United States
…continuum, from undergraduate medical education to faculty development. Specific needs of the Department may vary over time, but may range from development / implementation and study of…
Added just now
Quality Assurance Inspector - B Shift
Arvato Bertelsmann
Louisville, KY
…inspections, monitoring processes, and supporting production operations. This role works closely with Operations and Quality leadership to meet customer specifications, maintain service…
Added just now
B
Retail Front End Supervisor - Full-Time
Burlington
LOUISVILLE, KY
- $15 to $17 USD / hour
- Full-time
…Management in the areas of Merchandising, Customer Service, Operations, and Human Resources. This leadership position is the stepping-stone to a management role within our expanding…
Added just now
Sales Operations Analyst
GE Appliances, a Haier company
Louisville, KY
Onboard, train & manage Commercial Development Program bubble assignments and Co-op/interns
Added just now
Occupational Therapist
Sevita
Louisville, KY
…attending conferences, etc.Attends departmental meetings for program development and establishing effective systems of operations team…
Added just now
MRI Manager Medical Imaging - $20,000 Sign On Bonus
RIH Rhode Island Hospital
United States
…procedures. Is responsible to provide a high-quality education program for incumbent staff. Supports designated student training program(s) for the department by assuring the training…
Added just now
Manager, Ecosystem Program
KPMG
Louisville, KY
Support budgeting, resource planning, operational administration, and development of program artifacts, planning materials, and executive reporting
Added just now
Regional Mobility Immigration Partner
Arvato Bertelsmann
Louisville, KY
The role also supports and coordinates Arvato USA's employer-sponsored immigration program, working closely with US HR and external immigration counsel. The scope will include retained…
Added just now
Senior Manager, Product – Ductless Residential HVAC
GE Appliances, a Haier company
Louisville, KY
…limited oversight, the Senior Manager, Product bridges technical development and market requirements to deliver profitable, competitive ductless solutions aligned with broader Residential…
Added just now
K
Senior Associate, ECC Contracts
KPMG
Louisville, KY
- $7.25 USD / hour
…It's also enabled by our culture, which encourages individual development, embraces an inclusive environment, rewards innovative excellence and supports our communities. With qualities like…
Added just now
Manufacturing Engineering Co-op (Summer/Fall 2027)
Collins Aerospace
Louisville, KY
U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract.

Closed listing

Parexel

Early Clinical Scientist

Boston, MA, United States

This opening has closed.

The original listing is kept below for reference.

Find open jobs More jobs with this employer

About employer

Job details

Posting language: English
Posted: Oct 2, 2026

Similar jobs hiring now

Search current openings

Original job description

Archived listing. The details below describe a past opening.

Parexel FSP has exciting opportunity for a Clinical Scientist! The Early Clinical Scientist (ECS) may lead or support an early phase clinical study or studies, depending on size/complexity. The ECS is accountable for the clinical/scientific execution of the protocol.

Key Accountabilities:

Oversight/Leadership

Responsible for coordinating the design, planning and execution of early phase clinical trials in collaboration with the Clinical Director, and internal/external team members
Oversees trials within and/or across program(s)/therapeutic areas and ensures excellence in execution/compliance to support study objectives and data validity
Manages trial and program projects including team activities (i.e. meetings, document/collaborative workspace management, etc.)
Manages internal/external team performance to achieve project objectives and resolves project performance issues if they arise
Conducts real-time oversight of ongoing trials to identify and mitigate patient, study design, data or study conduct issues

Clinical Trial Operational Delivery

Monitors clinical safety assessment and risk management of compounds
Provides risk assessment and contingency planning, under accelerated timelines
Reviews and interprets clinical trial data
May conduct on-site study monitoring, including site training and supervision of complex, novel endpoint/biomarker collection processes
Co-authors clinical sections of protocols, clinical investigator brochures, clinical study reports and ensures documents are completed in accordance with applicable standards
Develops study operational documents with input from team members (e.g. site monitoring plan, study operations manual, informed consent, etc.)
May be required to review budgets and approve invoices for payments to vendors.

Compliance with Parexel Standards

Complies with required training curriculum
Completes timesheets accurately as required
Submits expense reports as required
Updates CV as required
Maintains a working knowledge of and complies with Parexel processes, ICH-GCPs and other applicable requirements

Skills:

MS Office Suite Experience Required– including Word, Excel, Power Point, and Teams
Strong team collaboration, leadership, communication (written and verbal), issue identification and resolution skills
Proficient in written and spoken English
Proficient in local language (as applicable)
Ability to manage multiple projects and varied tasks and prioritize workload with attention to detail
Ability to manage complex operations and projects under accelerated timelines
Ability to partner effectively with internal and external teams to achieve results
Ability to quickly develop a working scientific knowledge of different therapeutic areas
Ability to build knowledge and skills to effectively manage additional processes/procedures
Ability to build knowledge and skills to effectively manage additional processes/procedures

Knowledge and Experience:

Experience in managing CROs from the Sponsor side for Phase 1 clinical trials
Use of Clinical Trial Management and Trial Master File systems
Authoring Protocol Concepts
Facilitating a Trial Team including cross functional partners such as regulatory, clinical supplies managers, data managers, statisticians, programmers, procurement, etc.
Reviewing the following: protocol, ICF, IB, CSR, biomarker process, site and medical monitoring plans, risk assessment, protocol deviations
Understanding of clinical research development process from program planning to regulatory submission
Scientific, medical and/or safety writing and reporting (at least one is required)
Knowledge of GCP, ICH guidelines and regulatory requirements
Familiarity with early drug development processes

Education:

Degree in Life Sciences
Bachelor’s degree and ≥7 years related* experience OR
Master’s degree and ≥5 years related* experience OR
PhD or doctorate degree and ≥1 year related experience

EEO Disclaimer

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

About employer

Report this job