Study assistant Job at EdEx (Dartford)

Study Assistant / Academic Tutor

Study Assistant / Academic Tutor position at a Secondary School in Brent support...

Location

United Kingdom , Brent, London

Salary:

Not provided

EdEx

Expiration Date

Until further notice

Requirements

Strong academic background
Educated to undergraduate level at a minimum
Passion for education, learning and high achievement

Job Responsibility

Support students aged 11-19 in accessing learning resources
Work alongside families of identified students to support their progress and attainment
Supervise and provide support for student/s, including those with identified needs
Assist with development and implementation of Individual Education/Behaviour Plans and Personal Care programmes
Establish constructive relationships with students
Promote inclusion and acceptance of all students
Encourage students to interact with others and engage in activities
Set challenging expectations and promote self-esteem and independence

Fulltime

Clinical Research Coordinator I

Supports Frenova Renal Research by providing administrative and clinical support...

Location

United States of America , Mishawaka

Salary:

Not provided

Fresenius Kidney Care Eupora

Expiration Date

Until further notice

Requirements

High School Diploma required
Associate’s Degree or Certified Medical Assistant preferred
2-4 years of experience of related experience preferred
Minimum 18 months experience in a medical setting and/or clinical research setting required
Willingness to obtain research specific training as needed
Ability to meet deadlines for multiple concurrent projects
Ability to understand and follow study specific protocol and direction
Ability to understand a patient medical record
Attention to detail required
Good computer skills including MS Excel

Job Responsibility

Utilizes experience and knowledge to act as a resource and provide on-going leadership and support to Clinical Research Assistant I
Conducts on the job training for Clinical Research Assistant I as requested
Researches and identifies research related issues and discrepancies
Obtains and prepares regulatory/essential documents throughout the duration of a study
Ensures documents and forms are compiled and submitted in a timely manner
Assists with maintaining constant communication with Institutional Review Boards, study sponsors, dialysis facility, practice and field staff
Assists with the contracting process, document preparation and execution
Interfaces with potential study subjects for the purpose of promoting participation in research studies
Assists with screening subjects for participation eligibility
Assists with and documents the obtaining of informed consent according to GCP

What we offer

Healthcare
Continuing Education
Paid Time Off
Collaborative Environment
Additional Perks
401(k) Retirement Saving

Fulltime

Psychology Graduate SEN Teaching Assistant

Psychology Graduates & Students – Start Your Career as a SEN Teaching Assistant....

Location

United Kingdom , Bristol

Salary:

Not provided

AFFINITY WORKFORCE

Expiration Date

Until further notice

Requirements

Is studying or has graduated in psychology (or a related field) and wants to apply their knowledge practically
Is confident working with challenging behaviour and can adapt strategies to suit individual needs
Can provide 1:1 or 2:1 or classroom tailored support to help pupils reach their potential
Demonstrates strong communication and behaviour management skills
Is proactive, resilient, and enthusiastic about inclusion
Is committed to continuous learning and professional growth

Job Responsibility

Apply psychological concepts such as behaviour management, developmental theory, and communication strategies in real-world settings
Gain practical experience supporting children with Autism Spectrum Condition (ASC), Profound and Multiple Learning Difficulties (PMLD), Severe Learning Difficulties (SLD), and complex needs
Work across five specialist sites – Infants, Juniors, Secondary, Sixth Form, and Alternative Provision – giving you diverse exposure to different age groups and developmental stages
Receive ongoing training and mentoring, including Team Teach and Trauma-Informed Practice, to complement your academic studies
Build transferable skills in observation, intervention, and tailored support that will strengthen applications for postgraduate study or careers in clinical, educational, or occupational psychology
Supporting pupils with a wide range of needs, including: Autism Spectrum Condition (ASC), Profound and Multiple Learning Difficulties (PMLD), Severe Learning Difficulties (SLD), Complex Needs

What we offer

Competitive salary and referral bonuses
Excellent training and development opportunities – including Team Teach and Trauma-Informed Training
Supportive and friendly team environment
Will have a dedicated point of contact for ongoing guidance and support throughout their placement or employment
Clear guidance and mentorship from experienced professionals
Opportunities to work across multiple specialist school sites
A strong focus on staff wellbeing

Study Delivery Associate

The Study Delivery Associate provides essential administrative and operational s...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s degree
Associate’s degree and 4 years of clinical execution experience
High school diploma / GED and 6 years of clinical execution experience
2 years' work experience in life sciences or medically related field
1 year of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
Experience working on global clinical trials
Expertise in clinical trial processes, operations, and oversight in biotech, pharmaceutical, or Contract Research Organization environments
Strong skills in using MS Word, Excel, PowerPoint, and other relevant software
Experience with tracking and filing of essential documents
Working knowledge of CTMS, eTMF, EDC, and Microsoft Office tools

Job Responsibility

Support the setup and maintenance of study-level trackers, dashboards and timelines
Communicate study progress, timelines and deliverables to the Study Delivery Manager
Assist with tracking and following up on study actions, including risk mitigation actions
Assist with the preparation and record keeping of risk & quality reviews
Ensure completion of study team training and inspection readiness activities
Assist with trial-related events, global site communications, and logistics for investigator meetings
Support study start-up activities, including system setup, supplier access management, ICF tracking and document readiness
Support vendor relationships and site engagement strategies
Manage shipment, reconciliation and analysis of biological samples
Coordinate investigational product logistics

What we offer

Reasonable accommodation for individuals with disabilities

Nurse Practitioner

New Graduate Primary Care Program designed specifically for newly graduated or l...

Location

United States , Greensboro

Salary:

87035.00 - 187460.00 USD / Year

CVS Health

Expiration Date

Until further notice

Requirements

NP/PA with less than 12 months of clinical experience
Active and unrestricted Family Nurse Practitioner or Physician Assistant license
Ability to provide holistic, evidence-based care, including STI prevention and education
Authorized to order/administer immunizations (e.g., COVID-19, flu, TB, Depo)
Basic Life Support (BLS) certification, including CPR and AED
Willingness to complete DOT certification within 30 days of hire
Ability to pass a respirator FIT test and wear a mask when required
Master's degree from an accredited Family Nurse Practitioner program, National Board Certification and state licensure to practice as an Advanced Practice Nurse or Physician Assistant
Or in select states, Master of Science in Physician Assistant Studies (or other health-related master's degree or equivalent experience together with Bachelor of Science in Physician Assistant Studies) with current National Board Certification and State of Employment license to practice in the role

Job Responsibility

Deliver evidence-based primary and family care, including assessment, diagnosis, treatment, and health counseling
Perform administrative tasks such as clinic opening/closing, inventory, insurance verification, and payment collection
Conduct routine exams and diagnostic tests to support accurate diagnosis and treatment
Collaborate with other healthcare professionals to ensure comprehensive care
Promote preventive care and wellness through screenings, chronic condition management, and behavioral health support

What we offer

Autonomy to manage your own practice with strong clinical and organizational support
Flexible scheduling and a focus on work-life balance
Comprehensive training and access to industry-leading tools and resources
Evidence-based clinical decision support tools
Career growth and development opportunities within a Fortune 10 company
No after-hours charting—complete documentation during your shift
Affordable medical plan options
401(k) plan with matching company contributions
Employee stock purchase plan
No-cost wellness screenings, tobacco cessation and weight management programs

Fulltime

Clinical Trials Assistant

The Medical Affairs team collaborates with the leaders of Sleep, Respiratory Car...

Location

Australia , Sydney

Salary:

Not provided

ResMed

Expiration Date

Until further notice

Requirements

Bachelor’s degree in relevant studies
Ability to support multiple clinical studies on relatively tight timelines and prioritise multiple tasks
Developing and maintaining relationships with internal and external stakeholders
Follows standard practices and procedures and applies basic theories, concepts, principles and methodologies in analyzing situations or data
Receives instruction, guidance and direction from others.
Proficient in software applications such as Outlook, Word, Excel and PowerPoint

Job Responsibility

Participates in the set-up and implementation of clinical studies through communication between the CDS and the study site.
Supports the CDS to ensure that all required devices and materials for the study are prepared and available
Ensures the clinical study database and Case Report Forms (CRFs) are prepared in advance of the study commencing
Assist in monitoring of the clinical study data during the conduct of the study to ensure compliance to the study protocol and applicable Work Instructions
Assists in audits and Regulatory Inspections as required
Verifies study documentation files and finalises the study closure reports at the completion of the clinical study
Appropriately documents and archives study data and documentation as per Work Instructions following the completion of the clinical study

Fulltime

Study Delivery Associate

The Study Delivery Associate provides essential administrative and operational s...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s degree
Associate’s degree and 4 years of clinical execution experience
High school diploma / GED and 6 years of clinical execution experience
2 years' work experience in life sciences or medically related field, including 1 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
Experience working on global clinical trials
Expertise in clinical trial processes, operations, and oversight in biotech, pharmaceutical, or Contract Research Organization environments
Strong skills in using MS Word, Excel, PowerPoint, and other relevant software for documentation, data management, and trial support
Experience with tracking and filing of essential documents such as protocols, informed consent forms, and regulatory submissions
Working knowledge of CTMS, eTMF, EDC, and Microsoft Office tools
Ability to maintain accurate and timely data entry

Job Responsibility

Support the setup and maintenance of study-level trackers, dashboards and timelines
Communicate study progress, timelines and deliverables to the Study Delivery Manager
Assist with tracking and following up on study actions, including risk mitigation actions
Assist with the preparation and record keeping of risk & quality reviews
Ensure completion of study team training and inspection readiness activities to maintain compliance with regulatory requirements
Assist with trial-related events, global site communications, and logistics for investigator meetings
Support study start-up activities, including system setup, supplier access management, ICF tracking and document readiness
Support vendor relationships and site engagement strategies
Manage shipment, reconciliation and analysis of biological samples
Coordinate investigational product logistics, ensuring compliance with reconciliation processes

What we offer

Reasonable accommodation for individuals with disabilities to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment

Study Delivery Associate

The Study Delivery Associate provides essential administrative and operational s...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s degree
Associate’s degree and 4 years of clinical execution experience
High school diploma / GED and 6 years of clinical execution experience
2 years' work experience in life sciences or medically related field
1 year of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
Experience working on global clinical trials
Expertise in clinical trial processes, operations, and oversight in biotech, pharmaceutical, or Contract Research Organization environments
Strong skills in using MS Word, Excel, PowerPoint, and other relevant software
Experience with tracking and filing of essential documents such as protocols, informed consent forms, and regulatory submissions
Working knowledge of CTMS, eTMF, EDC, and Microsoft Office tools

Job Responsibility

Support the setup and maintenance of study-level trackers, dashboards and timelines
Communicate study progress, timelines and deliverables to the Study Delivery Manager
Assist with tracking and following up on study actions, including risk mitigation actions
Assist with the preparation and record keeping of risk & quality reviews
Ensure completion of study team training and inspection readiness activities to maintain compliance with regulatory requirements
Assist with trial-related events, global site communications, and logistics for investigator meetings
Support study start-up activities, including system setup, supplier access management, ICF tracking and document readiness
Support vendor relationships and site engagement strategies
Manage shipment, reconciliation and analysis of biological samples
Coordinate investigational product logistics, ensuring compliance with reconciliation processes

What we offer

Reasonable accommodation for individuals with disabilities

Study assistant

EdEx

Location:
United Kingdom , Dartford

Category:
Education

Contract Type:
Employment contract

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
November 24, 2025

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