Staff Associate II Job at jobRxiv

Clinical Research Associate II

Clinical Research Associate - Remote - FSP. ICON plc is a world-leading healthca...

Location

Greece , Athens

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor's degree in a scientific or healthcare-related field
Minimum of 2 years of experience as a Clinical Research Associate
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Strong organizational and communication skills, with attention to detail
Ability to work independently and collaboratively in a fast-paced environment
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

Job Responsibility

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
Collaborating with investigators and site staff to facilitate smooth study conduct
Performing data review and resolution of queries to maintain high-quality clinical data
Contributing to the preparation and review of study documentation, including protocols and clinical study reports

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Fulltime

Senior Clinical Research Associate or Clinical Research Associate II

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

United States , Blue Bell

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor's degree in a scientific or healthcare-related field
Minimum of 1-year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Strong organizational and communication skills, with attention to detail
Ability to work independently and collaboratively in a fast-paced environment
Ability to travel at least 60% of the time (international and domestic - fly and drive)

Job Responsibility

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
Collaborating with investigators and site staff to facilitate smooth study conduct
Performing data review and resolution of queries to maintain high-quality clinical data
Contributing to the preparation and review of study documentation, including protocols and clinical study reports

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Loan Agency Services, Associate II

Discover the future of debt capital markets. We’re experts at adapting and innov...

Location

United States , Chicago

Salary:

42500.00 - 75000.00 USD / Year

Alter Domus

Expiration Date

Until further notice

Requirements

Bachelor’s degree in accounting, finance, economics, a related field, or commensurate work experience
2+ years of experience in bank loan agency, syndication or investment management operations experience
Responsive, friendly, professional, and proactive communication approach
Deadline-driven and highly organized with exceptional attention to detail
Ability to independently research, analyze and resolve complex problems and quickly learn new concepts
Working knowledge of fundamental financial, accounting and operations concepts
High proficiency in Microsoft Excel and experience with Bloomberg and other loan research tools a plus

Job Responsibility

Act as liaison between borrowers and lenders, collaborate with other parties within the industry, including legal counsel, trustees and other third party service providers
Maintain a working knowledge of all relevant portfolios and deal related documentation
Reference, understand and extract Credit Agreement and governing document information to ensure compliance and update the Agency system accordingly
Use judgment, interpretation and problem-solving to understand loan related information
Calculate, invoice and disburse all deal related fees
collect and disburse interest, principal, fee payments and new borrowing funds
Coordinate funds movement for initial funding and closing
Provide training to Associate level staff on policies and procedures
Ensure proper system set-up including maintenance of changing deal attributes
Understand services offered and risks as it relates to Agency and alert Manager of out of scope requirements, risk issues, etc

What we offer

Support for professional accreditations such as ACCA and study leave
Flexible arrangements, generous holidays and birthday leave
Continuous mentoring along your career progression
Detailed career pathway with structured support
Exclusive access to online learning
Active sports, events and social committees
Employee Assistance Program
Employee Share Plan

Fulltime

Clinical Research Associate II or Senior Clinical Research Associate

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

Brazil , Belém do Pará

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor's degree in a scientific or healthcare-related field
Solid experience as a Clinical Research Associate in CROs or pharma companies
Based in Belém do Pará, or nearby locations
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Strong organizational and communication skills, with attention to detail
Ability to work independently and collaboratively in a fast-paced environment

Job Responsibility

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
Collaborating with investigators and site staff to facilitate smooth study conduct
Performing data review and resolution of queries to maintain high-quality clinical data
Contributing to the preparation and review of study documentation, including protocols and clinical study reports

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Medical Lab Scientist II

At Boston Children’s Hospital, the quality of our care – and our inclusive hospi...

Location

United States , Needham

Salary:

33.60 - 53.77 USD / Hour

Boston Children's Hospital

Expiration Date

Until further notice

Requirements

Associate’s Degree AND successful completion of an ASCP/NAACLS accredited Medical Technology/Medical Laboratory Science program required
Bachelor’s Degree AND successful completion of an ASCP/NAACLS accredited Medical Technology/Medical Laboratory Science program preferred
Minimum 3 years of Clinical Lab Science experience required
5 years Clinical lab experience preferred
National certification preferred
Certification required for related science degreed individuals

Job Responsibility

Performs a variety of routine and highly specialized diagnostic tests and specialized procedures
Assures quality of the results and communicates relevance of results to other health care professionals
Performing a variety of moderate and highly complex and diagnostic laboratory testing under general supervision in the laboratory
May perform specialized procedures in special laboratory sections unique to each laboratory’s discipline
Evaluating whether the results are abnormal/critical and takes appropriate action internally/externally according to laboratory guidelines
Recording results of tests with all supporting documentation for clinical interpretation
Performing regularly scheduled quality control, preventative maintenance, and calibration of equipment according to laboratory guidelines. Performs all troubleshooting and repair
Participating in department continuing education including training program expanding scope of knowledge
Providing general assistance to less experienced laboratory personnel
Communicating principle/theory to physicians and other professional staff

What we offer

$7,500 one time sign on bonus
flexible schedules
affordable health, vision and dental insurance
child care and student loan subsidies
generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement
cell phone plan discounts
discounted rates on T-passes

Fulltime

Biomedical Equipment Technician II

The Biomedical Equipment Technician II (BMET2) provides clinical equipment servi...

Location

United States , Marietta

Salary:

Not provided

Wellstar Health System

Expiration Date

Until further notice

Requirements

High School Diploma General
Associates Electrical Engineering or Associates Biomedical Engineering or Associates Mechanical Engineering
GADL - Georgia Driver's License or VSDL - Valid State Driver's License
Minimum 3 years of experience in supporting medical devices and systems in a hospital environment
Minimum 3 years Knowledge of electronic digital circuitry and understanding of electronic and electro-mechanical devices
Proficient in Microsoft Office software including Word, Excel, and PowerPoint
Capable of interpreting building architectural and systems drawings and information
Able to compose and deliver presentations regarding medical devices and systems to clinical staff
Working knowledge of Security Protocols

Job Responsibility

Perform calibrations and repairs on equipment as assigned
Demonstrate knowledge of safe and approved troubleshooting techniques on medical devices
Read schematics and service manuals, consult with vendors and service representatives to assist in troubleshooting
Utilize test equipment and complete repairs in a time and cost-effective manner with patient safety as the primary focus
Document work performed and any significant performance data accurately and in a timely manner
Operates as part of a team of engineers responsible for providing in depth technical knowledge required to implement, manage, upgrade and support many applications and interoperability into EPIC and other repositories
Responds to service calls to evaluate, diagnose, and perform corrective and preventative maintenance on biomedical equipment which requires moderate intervention
Performs safety acceptance testing on new medical equipment and on hospital equipment returned after service
Documents all repair, maintenance, installation, and other activity in a timely fashion using the departments equipment management software and other mechanisms as needed
Update/Install medical equipment to include security protocols and work with customers to provide design solutions maintaining technical and application standards

Fulltime

Biopharm Manufacturing Associate II

We make and supply medicines and vaccines all around the globe and our teams own...

Location

United States , King of Prussia

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

BS/BA degree, with cGMP manufacturing experience
OR an Associate’s degree from Montgomery county community college in Biotechnology or related technical field with cGMP manufacturing experience
OR High School degree, 1+ years of cGMP manufacturing experience.

Job Responsibility

Perform production operations including fermentation or cell culture operations, preparation of solutions, chromatographic separation, filtration and concentration operations, autoclave and parts washing of process assemblies, and area cleaning/upkeep
Be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time
Participate in safety and compliance initiatives, as well as investigations
Engage in the GSK Production System to continuously improve safety, quality, and schedule/cost performance
Demonstrate GSK Values (Patient Focus, Transparency, Respect, & Integrity) and Expectations (Courage, Accountability, Development, & Teamwork) on a daily basis by engaging positively with team members and production support groups
Under the direction of senior personnel, performs a variety of largescale production operations, interacting with automated equipment and monitoring/processing data
Participate in safety and compliance initiatives, investigations, and help solve technical and organizational problems while working with different teams of experts
With good documentation and data integrity practices, safely and compliantly completes and documents daily manufacturing tasks per standard operating procedures, batch document instructions, and logbooks
Proactively works with senior staff to achieve competency in production operations
Supports in cross-functional activities, such as engineering actions, validation actions and Tech Transfer actions, including proactive safety and compliance input prior to execution

Fulltime

Staff Nurse

Becoming a Nurse at University Health is a great way to step up and be there for...

Location

United States , San Antonio

Salary:

31.00 - 56.00 USD / Hour

University Health

Expiration Date

Until further notice

Requirements

Minimum of one year experience required
Verification of course completion in accordance with all American Heart Association Basic Cardiac Life Support and Health Care Provider guidelines is required
BSN highly preferred
Current license from the Board of Nurse Examiners of the State of Texas to practice as a registered nurse is required
Must have a current AHA BLS Healthcare Provider or AHA BLS Instructor Provider card

Job Responsibility

Provides basic leadership skills for assigned patients
Collaborates with other departments
Begins process of proactive thinking when implementing the plan of care
Serves as mentor to the staff nurse and ancillary personnel
Receives mentoring from Staff Nurse II and III and Patient Care Coordinator

What we offer

Medical: Excellent coverage for individuals and families with very low premiums and co-pays, and ZERO co-pays for medications filled at University Health
Dental
Vision
Pet insurance
Flexible and health spending accounts
Paid Time Off (PTO): Generous accrual rates that start on day one
Retirement: 457(b) and 403(b) deferred compensation programs
Education Reimbursement: Including college tuition reimbursement up to $600 per semester, continuing education up to $400 and certification reimbursement
Life and Disability: Basic life paid by University Health, with optional plans for life and disability insurance
Health and Wellness: Employee discounts, including gym memberships, employee health clinic, healing arts program, community events

Parttime

Staff Associate II

jobRxiv

Location:
United States

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 05, 2026

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jobRxiv

Location:United States

Category:Research and Development

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Job Description:

Job Responsibility:

Requirements:

Additional Information:

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