Associate Research Specialist Job at Children's Hospital Los Angeles (Los Angeles)

Associate Research Specialist

The Associate Research Specialist (ARS) will be involved in pediatric neural can...

Location

United States , Los Angeles

Salary:

43680.00 - 61953.00 USD / Year

Children's Hospital Los Angeles

Expiration Date

Until further notice

Requirements

Experience working in a laboratory environment required
Preferred 1+ years experience performing laboratory research (previous work in a biology research lab for at least 6 months and have at least 3 months of experience performing mammalian cell culture)
Previous experience working with live mice and human stem cells is preferred
Bachelor’s degree or equivalent experience in a scientific field
Applicants must have completed their bachelor’s degree by their anticipated start date
Candidates must be committed to working for at least 2 years

Job Responsibility

Conducts routine laboratory research procedures
Follows protocol to perform experiments
Tabulates data and may assist with analysis
Performs routine equipment maintenance and orders supplies
May provide instruction to support personnel
Maintain and differentiate human stem cells
Clone DNA constructs
Perform genome editing using CRISPR
Perform transduction/transfections, flow cytometry, western blot, RT-qPCR, immunofluorescence, immunohistochemistry and mouse surgeries
Rotate with 2-3 other lab mates to maintain cell cultures over the weekends

What we offer

Competitive compensation package
Robust benefits program

Fulltime

Clinical Research Associate Specialist 2

A remote Clinical Research Associate role based out of Irvine, California, suppo...

Location

United States , Irvine

Salary:

65.00 - 85.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

3–4 years in clinical research as a CRC or CRA, including quality assurance/control and regulatory compliance in the healthcare industry
Experience with electronic data capture (EDC) systems
Experience with Veeva or a similar clinical trial management platform
Remote monitoring and site management
Electronic data capture (EDC) proficiency
Veeva or equivalent platform experience
Knowledge of regulatory compliance and ICH/GCP guidelines
Strong data collection and documentation skills
Cross-functional collaboration and stakeholder communication
Process improvement mindset

Job Responsibility

Perform remote monitoring visits - qualification, initiation, interim monitoring, and close-out — and complete reports per the study monitoring plan
Provide cross-functional operational support throughout the study lifecycle
Investigate data and documentation discrepancies and contribute to process improvements to reduce recurrence
Support, interface, and collaborate with site personnel, IRBs/ECs, contractors, vendors, and cross-functional company personnel
Build and maintain strong working relationships with internal partners (Clinical Operations, Regulatory Affairs, Quality, R&D) and site personnel (Investigators, CRCs, research nurses)
Assist with site remediation activities as applicable
Complete and maintain relevant training specific to Medical and Clinical Affairs, BU-specific, and study-specific requirements
Identify opportunities and propose solutions to improve process efficiency within and across related functional areas

Fulltime

New

Associate Research Engineer/ Specialist

Are you interested in joining a dynamic team at GKN Aerospace to advance cutting...

Location

Sweden , Trollhättan

Salary:

Not provided

NearYou Sverige AB

Expiration Date

Until further notice

Requirements

MSc in Mechanical Engineering, Materials Engineering, Production Engineering, Industrial Engineering, Physics or a related field
alternatively, a BSc in a relevant discipline with at least 2 years of industry experience
Strong written and verbal communication skills, with the ability to produce clear technical reports and deliver effective presentations
Fluent in English
Develops new NDT processes, transitions emerging technologies into production, and ensures continuous improvement through effective lessons learned, knowledge capture, and process development
Solid understanding of manufacturing processes, including additive manufacturing techniques
Knowledge of non-destructive testing (NDT) methods
Hands-on experience with X-ray Computed Tomography and/or radiography is considered a plus
Experience in Computer-Aided Engineering (CAE) tools is advantageous
Programming skills and/or experience with AI-related methods are considered an asset

Job Responsibility

Perform inspection and evaluation of specimens produced through Additive Manufacturing (AM) processes
Correlate inspection results to support and enable AM process and material development
Work closely with process development teams to improve manufacturing quality and reliability
Contribute to the development of inspection methodologies for advanced aerospace components
Analyze inspection data to drive process optimization and defect understanding

What we offer

Collective agreement conditions for salary, insurance, pension and holiday
Consultant manager support
Opportunity to meet different company cultures and gain experience from various industries

Fulltime

Senior Clinical Research Associate/Clinical Research Associate II - Oncology

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

United States

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) in a CRO or pharma organization
Preferred therapeutic experience in Oncology
Global clinical trial experience preferred
Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Must be fluent in English and in the native language(s) of the country they will work in
Travel (60-80%) within area is required
Valid driver’s license and passport required
Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
Demonstrated knowledge of global and local regulatory requirements
Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)

Job Responsibility

Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and sponsor standards to achieve project goals, timelines and quality
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
During study conduct, serve as the primary point of contact for assigned investigator sites
Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
Provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
Attend investigator meeting when required (virtual or F2F)
Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators
Partner with SCP and the study team to define and support recruitment initiatives at site level

What we offer

Flexible work arrangements
Career growth and development
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced Technology

Fulltime

New

Associate Specialist - Technical Applications Group

The Associate Specialist Technical Applications Group (TAG) supports the develop...

Location

United States , Boca Raton

Salary:

Not provided

Nestlé Purina

Expiration Date

Until further notice

Requirements

Bachelor's degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Food Science, or related scientific discipline
0–1 year of relevant experience (internships, co-ops, or entry-level experience considered)
Basic understanding of formulation development and manufacturing processes
Familiarity with laboratory or manufacturing environments and nutraceutical, pharmaceutical, or consumer health products
Working knowledge of GLP and cGMP practices
Proficiency with Microsoft Office (Word and Excel)
Strong technical writing and documentation skills
Knowledge of scientific principles related to formulation and manufacturing processes
Ability to work in environments with exposure to powders, chemicals, and allergens

Job Responsibility

Support formulation development, evaluation, and process improvement for nutritional and solid dose products
Execute laboratory studies, development trials, and assist with industrial trials and production support
Collect, analyze, and report data
prepare technical summaries and documentation
Support scale-up, validation, and technology/process transfer to internal and external manufacturing sites
Provide technical support for manufacturing, including troubleshooting, process improvements, and cost savings initiatives
Create and maintain technical documentation (raw material specifications, batch records, change controls, deviations, transfer documents)
Maintain laboratory records, equipment, and workspaces
Identify and support continuous improvement initiatives and elimination of non-value-added activities
Research and share scientific and technical information with the team

Fulltime

New

Associate Specialist, Accounts Payable and Receivable (US)

We are seeking a detail-oriented and self-motivated Accounts Payable (AP) Paymen...

Location

India , Hyderabad

Salary:

Not provided

Randstad

Expiration Date

December 21, 2026

Requirements

Exposure to accounts payable/P2P
payments task
invoice processing
working knowledge of JDE and COUPA

Job Responsibility

Lead the end-to-end execution of daily and ad-hoc payment runs
Monitor payment run calendar and make sure payments are completed on time
Monitor the JDE revision queue regularly to ensure invoices are successfully interfaced into the system
Proactively monitor, research, and resolve ACH returns and rejects
Act as the primary point of contact for banking portals
Audit payment batches against supporting documentation
Identify discrepancies in the payment cycle and resolve them with minimal supervision
Respond to supplier queries about payment status
Look for opportunities to improve the payment process and support automation initiatives
Support month-end activities related to payments

Associate Specialist, Mid Office Operations

The ideal candidate will support Randstad Solutions delivery team to setup and m...

Location

India , Hyderabad

Salary:

Not provided

Randstad

Expiration Date

December 05, 2026

Requirements

HS Diploma Required
Some college graduation education preferred
4-7 years of related experience
Proficient with Microsoft Office tools including Word, Excel, PowerPoint, Outlook
Proficient utilizing Google Forms
Strong customer focus and customer service skills
Excellent communication, interpersonal and organizational skills
Demonstrated experience managing large, complex accounts or projects
Experience describing and documenting project requirements
Must be detailed oriented with a concern for quality expressed by continually initiating system and process improvements

Job Responsibility

Collaborate with management for goals and objective achievement
Ensure adherence to corporate guidelines and policies
Adhere to client and Company processes and quality procedures as defined
Communicate with management to provide status updates, reporting metric updates and identify any potential issues
Troubleshoot system, process, and document related issues
Create and update procedural documentation for internal distribution
Create and update Contract Set-ups per client contract documentation
Accurately add Talent to Contracts for time entry purposes
Provide back-up documentation to Billing team for customer to ensure timely payment
Research and resolve billing issues

Fulltime

Associate Specialist, Finance Business Partnering

Every year, we help hundreds of thousands of people find rewarding jobs in the e...

Location

India , Bangalore

Salary:

Not provided

Randstad

Expiration Date

July 16, 2026

Requirements

Proven work experience as an HR Onboarding Specialist, Payroll Specialist, or in a relevant combined HR Operations role
Hands-on experience with Human Resources Information Systems (HRIS)
Solid understanding of accounting fundamentals and payroll best practices
Basic knowledge of labor legislation and regulations of the field
Proficient in MS Office
Outstanding organizational ability with great attention to detail
Solid communication skills (verbal and written) and a strong team spirit
An ability to handle sensitive and confidential information with the highest degree of trustworthiness
High school diploma or equivalent
BSc/BA in Human Resources Management, Business, Accounting, or a relevant field is a strong plus

Job Responsibility

Communicate company and position details to new hires before their start date
Cascade company policies and employee handbooks
Gather and process all necessary onboarding paperwork, including contracts, non-disclosure agreements, and compliance forms
Roll out offers and collect essential onboarding documents
Ensure new hires have the necessary technical assistance (hardware/software setup, manuals, passwords, and guidelines)
Conduct Open house sessions regularly and address new hires' and existing employees' queries and grievances regarding contracts, policies, and payroll
Generate necessary internal system records (e.g., AL forms)
Process and manage the company's payroll with accuracy and efficiency
Gather information on hours worked for each employee and calculate the correct compensation, incorporating overtime, deductions, bonuses, etc., using a computer system
Keep track of hour rates, wages, compensation benefit rates, and new hire information within the payroll system

Fulltime

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Associate Research Specialist

Job Description

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What we offer

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