Regulatory Associate/Senior Associate Job at Capsticks Solicitors LLP (Birmingham, Leeds, London, Manchester or Winchester)

Associate/Senior Associate - Regulatory

This is an opportunity to work at the forefront of regulatory law. You will hand...

Location

United Kingdom , Birmingham, Leeds, London, Manchester or Winchester

Salary:

Not provided

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Has experience of handling regulatory, disciplinary, litigation, or advisory matters, with exposure to fitness to practise or professional standards work being advantageous
Has previous involvement in evidence gathering exercises, including working with witnesses and reviewing documentary material
Has experience of working with counsel and experts, including assisting with preparation for hearings
Can work collaboratively within a supervised team, contributing proactively to shared objectives, supporting colleagues, and engaging constructively with feedback
Is able to demonstrate an understanding of client needs and the wider public interest context of regulatory work.

Job Responsibility

Developing a clear case plan from the outset and advising on procedural and evidential issues
Ensuring all required factual evidence is identified and obtained
Acting as the main point of contact for witnesses and interviewing key witnesses, including those with complex, sensitive, or vulnerable circumstances
Supervising and reviewing witness statements prepared by paralegals
Instructing expert witnesses, reviewing expert reports, and obtaining clarification where needed
Preparing instructions to counsel (including internal advocates and external counsel) and attending conferences
Managing all follow up actions, maintaining momentum and case progression
Drafting charges or reviewing draft charges to ensure that they best reflect the evidence
Handling disclosure of unused material in line with regulatory expectations
Liaising with defence representatives in the lead up to hearings

What we offer

Competitive Salary
Hybrid Working
Inclusive employer
Reasonable adjustments to application and interview process

Fulltime

Associate/Senior Associate – Healthcare & Public Law (Inquests)

An established national law firm is looking to welcome an Associate or Senior As...

Location

United Kingdom , London

Salary:

62000.00 - 82000.00 GBP / Year

Jameson Legal

Expiration Date

Until further notice

Requirements

Qualified Solicitor with proven experience in healthcare inquests
excellent communication, attention to detail, and organisational skills
ability to work flexibly and proactively within a team
experience in healthcare law is ideal
experience in Court of Protection work or similar jurisdictions is a plus

Job Responsibility

Managing inquests both with and without a jury
providing advocacy and advice on governance, human rights, and patient-focused public law matters
supporting clients through investigations, complaints, and regulatory challenges
contributing to developing new services and initiatives

What we offer

Enhanced leave
flexible working
support for health and wellbeing
career development opportunities
practical resources

Fulltime

Associate/Senior Associate – Charity Governance and Commercial

This is an excellent opportunity to take on a broad, stimulating and varied role...

Location

United Kingdom , Putney

Salary:

Not provided

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Solicitor with experience in charity, corporate, or commercial law
4-6+ years’ PQE (flexible)
Experience in private practice, returning from a career break, relevant in-house experience, or law as a second career
Interest in the charity and not‑for‑profit sector
Proactive and curious approach to learning
Enthusiasm for getting involved in business development

Job Responsibility

Support charities of all sizes to meet legal and regulatory obligations
Act as a trusted advisor on strategic governance and commercial matters
Establish new charities and draft or update governing documents
Advise on company and charity law
Support charity restructures, mergers and incorporations
Provide guidance on commercial contracts, including brand licences and fundraising agreements
Take ownership of matters, manage your own workload, and build strong client relationships

What we offer

Competitive salaries
Generous package of benefits
Tailored training designed to support development and progression
Cohort-based career development programme
Access to cross-firm collaboration and internal network building

Clinical Research Associate/Senior Clinical Research Associate

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

Location

United States , Midwest, West region

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP
Good knowledge of relevant local regulations
Good medical knowledge and ability to learn relevant Client Therapeutic Areas
Basic understanding of the drug development process
Good understanding of Clinical Study Management including monitoring, study drug handling and data management
Bachelor’s degree in related discipline, preferably in life science, or equivalent qualification
Ability to travel nationally/internationally as required
Valid driving license per country requirements, as applicable
Oncology Experience required
Proficient in written and spoken English language required

Job Responsibility

Contributes to the selection of potential investigators
Accountable for study start-up and regulatory maintenance (in some countries)
Trains, supports, and advises Investigators and site staff in study related matters
Confirms that site staff have completed required training
Actively participates in Local Study Team (LST) meetings
Contributes to National Investigators meetings
Initiates, monitors, and closes study sites in compliance with Client Procedural Documents
Drives performance at the sites
Updates CTMS and other systems
Manages study supplies, drug supplies and drug accountability

What we offer

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

Fulltime

Clinical Research Associate/Senior Clinical Research Associate- FSP

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

Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP
Good knowledge of relevant local regulations
Good medical knowledge and ability to learn relevant Client Therapeutic Areas
Basic understanding of the drug development process
Good understanding of Clinical Study Management including monitoring, study drug handling and data management
Bachelor’s degree in related discipline, preferably in life science, or equivalent qualification
Excellent attention to detail
Good written and verbal communication skills
Good collaboration and interpersonal skills
Good negotiation skills

Job Responsibility

Contributes to the selection of potential investigators
As required, accountable for study start-up and regulatory maintenance
Trains, supports, and advises Investigators and site staff in study related matters
Confirms that site staff have completed and documented the required training appropriately
Actively participates in Local Study Team (LST) meetings
Contributes to National Investigators meetings
Initiates, monitors, and closes study sites in compliance with Client Procedural Documents
Drives performance at the sites
Updates CTMS and other systems with data from study sites
Manages study supplies, drug supplies and drug accountability at study site

What we offer

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

New

Bar Captain

Communicate service needs to chefs and stewards throughout functions. Total char...

Location

Malaysia , Petaling Jaya

Salary:

Not provided

Marriott Bonvoy

Expiration Date

Until further notice

Requirements

High school diploma or G.E.D. equivalent
At least 2 years of related work experience
At least 1 year of supervisory experience

Job Responsibility

Communicate service needs to chefs and stewards throughout functions
Total charges for group functions, and prepare and present checks to group contacts for payment
Ensure banquet rooms, restaurants, and coffee breaks are ready for service
Ensure proper centerpieces are displayed on every table
Inspect the cleanliness and presentation of all china, glass, and silver prior to use
Check in with guests to ensure satisfaction
Set tables according to type of event and service standards
Communicate additional meal requirements, allergies, dietary needs, and special requests to the kitchen
Maintain cleanliness of work areas throughout the day
Follow all company and safety and security policies and procedures

Fulltime

New

PACS Engineer

How would you like to work in a place where your contributions and ideas are val...

Location

United States , Augusta

Salary:

Not provided

Wellstar Health System

Expiration Date

Until further notice

Requirements

Bachelors Information Technology or Bachelors Computer Applications or Bachelors Biomedical Engineering
Advanced, hands-on experience administering, configuring, and supporting Sectra PACS / enterprise imaging
Hands-on experience with PACS solutions, with demonstrated Sectra proficiency
CIIP (Certified Imaging Informatics Professional) within 90 Days Required
PARCA (PACS Administrators Registry and Certification Association) within 90 Days Required

Job Responsibility

Design, implement, and optimize scalable PACS architectures that integrate with enterprise IT environments, including cloud-based and hybrid solutions
Ensure the PACS infrastructure is designed for high availability and fault tolerance to support hospital operations 24/7
Facilitate seamless integration with EHR, RIS, AI-driven diagnostic tools, and reporting systems using standardized protocols such as HL7 and DICOM
Enhance clinician workflows by designing user-centric PACS solutions that reduce inefficiencies and minimize image retrieval and load times
Develop strategies for load balancing, caching, and indexing to improve image retrieval speed and system responsiveness
Maintain in-depth knowledge of all applications and infrastructure supporting medical imaging, including networks, firewalls, and backend systems
Manage the lifecycle of PACS applications, ensuring efficient operation, preemptively resolving issues, and maintaining availability to support clinical operations
Monitor application performance, troubleshoot issues, and coordinate with technical teams to implement solutions
Ensure compliance with healthcare regulations and organizational policies
Oversee proper functioning of DICOM modalities, image routing, and data storage solutions

Fulltime

New

Senior Iam Engineer

Randstad Digital (Formerly Finite Recruitment) - Senior IAM Engineer. Canberra b...

Location

Australia , Canberra

Salary:

Not provided

Randstad

Expiration Date

July 19, 2026

Requirements

Australian Citizens ONLY
NV1 security clearance

Job Responsibility

Strong technical capability to support Business-as-Usual (BAU) operations for the One Identity Manager platform
Stabilizing and managing BAU activities at Level1 and Level2 to ensure operational stability and service continuity
Managing and supporting activities that overlap between BAU and Project delivery
Proactively monitor and troubleshoot complex issues in the One Identity Manager environment
Oversee the application of patches, updates, and upgrades to One Identity Manager and associated systems
Provide post-implementation support and develop detailed technical documentation
Perform daily Standard Operating Procedures (SOP’s) to maintain the quality of the operational platform
Configure and maintain IAM workflows, policies, and connectors to support BAU operations

Fulltime

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