RA Manager Jobs

Qa Engineer

For our client – worldwide leader in innovative IT and networking technologies –...

Location

United States , Columbia

Salary:

Not provided

Flint International

Expiration Date

Until further notice

Requirements

Bachelor’s Degree (CS, EE), or equivalent experience required
4-6years of industry experience in coding in testing and test methodologies
Strong in QA process, process definition and execution
Strong working knowledge on test automation tools for back end/UI
Strong working knowledge of agile/waterfall SW methodologies
Strong QA Process
Work experience on one or more Test Automation tools (Cucumber, Postman, test Ng, Selenium)
Work experience Scripting Language (python)
Strong written and oral English communication skills
Process oriented, self-starter, self-motivated individual

Job Responsibility

Understand the overall project, understand phase-wise requirements
Involve in requirements gathering, analysis and definition
Understand test planning strategy
Regression strategy, non-functional testing
Functional testing post integrations customizations patches
Staging through lab/test, pre-production, production
Test automations
Generate and own User guides for integrations
Work on testing tasks for phases/integrations
Automate testing using test tools, scripts

Team leader (operations)

Location

Salary:

Not provided

Flexisales Marketing Pvt. Ltd.

Expiration Date

Until further notice

Requirements

5+ years of Experience in Team Handling
Any Graduate
Post-Graduation Not Required
Looking to manage International B2B process
Ready to work in flexible shifts
Excellent verbal and written communication skills
Excellent interpersonal skills, with the ability to communicate with and relate to all levels both within and outside the organization
Should be dynamic, energetic, assertive besides excellent communication and presentation skills

Job Responsibility

Ensure completion of sales Process in place and Productivity
Ensures that company’s everyday activities run smoothly
Keep a track of how efficiently and effectively the organization is operating
Determine staffing requirements, and interview, hire and train new employees
Should have experience in handling team of 20 RA’s
Responsible for Performance management
Meeting the targets aligned
Quality Check of Team Members Performance and Share Feedback accordingly
To Provide Training to New Joiners as Required
To Supervise Team Adherence and Compliance are as per the Policies

Clinical Research Associate

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

Location

South Korea , Seoul; Remote

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Strong problem solving skills
Able to take initiative and work independently, and to proactively seek guidance when necessary
Excellent presentation skills
Client focused approach to work
Ability to interact professionally within a client organization
Flexible attitude with respect to work assignments and new learning
Ability to prioritize multiple tasks, and achieve project timelines
utilizing strong analytical skills to make decision autonomously due to the unpredictable nature of the issues that arise
Strong ability to make appropriate decisions in ambiguous situations
Willingness to work in a matrix environment and to value the importance of teamwork

Job Responsibility

Act as Parexel’s direct point of contact with assigned sites, accountable for quality and delivery during the start-up phase
Build relationships with investigators and site staff
Conduct, drive and manage country specific feasibility and/or site pre-qualification and qualification activities
Generate visit/contact reports, using judgment to identify site issues and problem solving to direct resolution
Develop strategy to configure, distribute, and collect, and review and approve, high quality country specific and/or site specific documents or essential regulatory documents (SRP) and any updated or amended regulatory documentation
Customize, review, and negotiate as needed, country/site specific Informed Consent Forms (ICF), translations, and customize and negotiate any amendments
Prepare and submit IRB/IEC and MoH/RA (if applicable) application(s), resolving conflicts, determining appropriate follow up until receipt of final approval
Submit all pertinent documentation to the trial master file as per project plans/sponsor/company policy
Forecast, develop, manage, and revise plans and strategies for IRB/IEC and MoH / RA submission/approval, Site activation, Patient recruitment & retention
Update and maintain appropriate Clinical Trial Management systems (CTMS) in a timely manner

What we offer

Patient-focused in everything we do
Supportive and inclusive environment
Career growth and development
Flexible work arrangements
Diverse therapeutic areas and project exposure
Advanced Technology

Finance Manager

We enable Plaid’s sustainable growth by providing financial insights and raising...

Location

United Kingdom , London

Salary:

Not provided

Plaid

Expiration Date

Until further notice

Requirements

Minimum 8 years’ experience in finance, accounting, or treasury within a fintech, payments, or EMI environment
Experience working in a firm authorised by both the FCA and DNB (or other EU regulators)
In-depth understanding of the Electronic Money Regulations (2011), Payment Services Regulations (2017), and equivalent EU frameworks under the PSD2/PSD3 and Wft
Proven experience managing safeguarding reconciliations, prudential calculations, and regulatory returns
Qualified accountant (ACA, ACCA, CIMA, RA, or equivalent)
Strong understanding of multi-currency safeguarding and cross-border finance
Excellent analytical and reporting skills
confident liaising with regulators and auditors
Exceptional attention to detail, integrity, and accountability

Job Responsibility

Lead all financial operations for UK/EU entities, including accounting oversight, reconciliations, internal controls, and management reporting
Prepare and maintain monthly/quarterly management accounts, prudential metrics, and capital adequacy reporting
Coordinate annual financial audits across jurisdictions and ensure audit readiness
Ensure consistent application of accounting and prudential standards across UK/EU entities
Manage outsourced UK/BV accounting service providers and partner closely with the US Accounting team to ensure a timely and accurate month-end close
Oversee treasury and liquidity management, ensuring adequate funding and strict segregation of client and corporate funds
Design, operate, and maintain the safeguarding control framework, including daily safeguarding reconciliations and timely investigation of discrepancies
Maintain safeguarding and trust accounts with regulated credit institutions and ensure breaches are logged and escalated appropriately
Prepare and coordinate the annual independent safeguarding audit and track implementation of recommendations
Produce and submit all required regulatory returns, including FCA REP021, FSA056/057 EMI returns, and DNB prudential reports

Fulltime

Rail System Safety Coordinator

At EKFB we’re shaping Infrastructure for a better tomorrow. All four of our part...

Location

United Kingdom , Milton Keynes

Salary:

Not provided

EKFB

Expiration Date

Until further notice

Requirements

Degree or equivalent experience in Engineering, Project Management or a related field
Experience in Rail Systems Design, Engineering or design, appreciation of NTSN and System Safety (CSM-RA) within infrastructure projects is highly desirable
Experience in infrastructure or civil engineering projects, ideally in a major project environment
Understanding of NEC contract mechanism (Early Warnings, Technical queries etc.)
Strong stakeholder management and communication skills
Ability to produce high-quality documentation and technical records
Proficient in Microsoft Office and project collaboration tools (e.g. SharePoint, Smart Connect)
Experience with assurance processes and document control

Job Responsibility

Lead stakeholder interfaces for Rail Systems and National Technical Specification Notices (NTSN) including chairing key meetings such as integration and design reviews
Manage and review NTSN Matrix and compliance evidence trackers
Support the Rail Systems discipline lead with review of and management of the Project Hazard record
Produce comprehensive meeting minutes capturing decisions and agreements in contractual and technical terms
Maintain and manage action trackers and issue logs, ensuring timely resolution and evidence-based closeout
Collaborate effectively with the client team while advocating for best-for-project outcomes
Liaise with design, construction, and assurance teams to address System safety and NTSN concerns
Draft and manage technical queries and contractual communications, with a working knowledge of early warnings, general communications, and change events
Support the Rail Systems Discipline Lead in production and maintenance of interface management plans, ensuring assurance processes are followed and client comments are resolved
Review short-notice construction changes, assess System Safety and NTSN impacts, and coordinate resolutions with stakeholders

What we offer

A competitive salary & benefits

Fulltime

New

Business Performance Senior Manager

The Business Performance Senior Manager is a member of the Transformation Execut...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree (scientific area) and 10 years of directly related experience OR Bachelor’s degree (scientific area) and 12 years of directly related experience
Knowledge of Regulatory principles
Working with policies, procedures and SOP’s
Comprehensive understanding of regulatory activities and how they impact other projects and/or processes
General knowledge of national legislation and regulations relating to medicinal products
General awareness of the registration procedures/challenges in the region for CTAs, MAs and all lifecycle management activities
Knowledge and experience in the international regulatory environment relevant for product area and development stage
Understanding of drug development
Able to anticipate regulatory Agency questions and potential responses
Demonstrate strong teamwork ability

Job Responsibility

Represent GRAAS at cross-functional MAL and Business Development-related forums, providing strategic input and thought leadership
Form and lead sub-function teams for integration and licensing activities, ensuring alignment with strategic objectives
Drive strategic solutions to complex business problems, leading analyses and negotiations with key decision makers
Lead Regulatory workstreams across all deal phases
Serve as Lead for all product licensing work, including integrations into and transitions out of Amgen
Closely partner with Regulatory Affairs (RA) Therapeutic Area Integration Project Lead and advise/instruct them on end-to-end process and details of planning and execution of acquisition integration
Act as their delegate as needed in cross-functional meetings
Assist with pre-deal close GRAAS due diligence
Develop and manage GRAAS integration workplan
Draft and manage any new controlled documents unique to the integration, such as Quality Integration PLANs and bridging process GDEs

What we offer

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

Intervention Support Assistant

We are seeking a dedicated Intervention Support Assistant to join our specialist...

Location

United Kingdom , Surrey (near Cranleigh)

Salary:

29064.00 GBP / Year

Pink Tile Education Ltd

Expiration Date

Until further notice

Requirements

Experience working with young people with SEMH needs or in a pastoral/intervention role
Strong communication and relationship-building skills
Ability to remain calm under pressure and respond effectively to challenging situations
A proactive, empathetic approach to supporting students’ emotional and behavioural development
A full, clean driving licence and access to a vehicle (due to location)
An enhanced DBS check (or willingness to obtain one)

Job Responsibility

Ensure pastoral and behaviour needs are met effectively both on and off-site
Communicate pastoral and behaviour concerns with parents, carers, and staff
Design and deliver interventions, programmes, and activities to support learning and self-management of behaviour
Act as an immediate responder to pastoral and challenging behaviour issues
Supervise and monitor reporting of significant incidents, including restrictive physical interventions, and analyse behaviour trends
Coordinate pastoral and behaviour support under the guidance of the Behaviour Lead/IST Operations Lead
Lead Student Voice initiatives within the school
Support Risk Assessment (RA) and Positive Behaviour Support (PBS) updates
Track and monitor social and emotional development across the student body

What we offer

Opportunities for professional development and career progression
A supportive environment where every day makes a difference

Fulltime

Cmc officer

Are you looking to grow professionally and make the most of your knowledge and s...

Location

Greece , Athens

Salary:

Not provided

Randstad

Expiration Date

December 30, 2025

Requirements

Minimum 2 years of experience in a R&D or CMC position
Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Studies or related sciences
Knowledge of the scientific (chemistry, manufacturing, control) documentation and registration requirements of the generic pharmaceutical products CTD dossier
Superb communication skills
Excellent knowledge and handling of both verbal and written English language

Job Responsibility

Compiling pharmaceutical CTD dossiers in eCTD format, followup until MAs are granted, and life-cycle maintenance of the world-wide registration of pharmaceutical products in regard to chemistry, manufacturing, control related documentation
Assist in the collection and evaluation of data to be included in module 3 of marketing authorization dossiers
Respond to queries (from regulatory authorities or clients) concerning dossiers, manage the process to respond to the CMC questions by involving all stakeholders both within and outside the company and following up agreed actions to respond as rapidly and completely as possible
Assist in keeping the dossier core files (Module 3 and corresponding QoS) fully up to date during registration procedures and because of variations
Participate in meetings related to registration procedures or when the CMC expertise is needed. Tightly collaborate with the RA and R&D Departments for assigned products
Prepare the variation and post-approval change packages and other necessary documents as required by the variation process
Ensure that all documents and records pertaining to the CMC Department are archived properly. Keep departmental database or other tracking system up to date
Review regulatory compliance protocols and/or reports, as requested
Participate in the change control system and variation process according to the established workflow and contributing to renewal applications

RA Manager

Eitan Medical

Location:
Israel, Netanya

Category:
IT - Administration

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
December 08, 2025

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RA Manager

Eitan Medical

Location:Israel, Netanya

Category:IT - Administration

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:December 08, 2025

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for RA Manager

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Location:
Israel, Netanya

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Contract Type:
Not provided

Job Posted:
December 08, 2025