CrawlJobs Logo

Junior Clinic Manager

https://www.office-angels.com Logo

Office Angels

Location Icon

Location:
United Kingdom , London

Category Icon

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

29000.00 - 30000.00 GBP / Year

Job Description:

Our client is seeking a proactive, organised, and personable Junior Clinic Manager to join their high-end medical clinic based on Harley Street. This role is ideal for someone who thrives in a fast-paced environment, enjoys delivering exceptional patient care, and excels at keeping operations running smoothly behind the scenes. You'll act as the face of the clinic, supporting both patients and the medical director to ensure every client receives a premium experience from the moment they enquire through to aftercare.

Job Responsibility:

  • Warmly greet patients and provide a professional front-of-house experience
  • Manage incoming enquiries across phone, WhatsApp, Instagram DM, website forms, and email
  • Confirm appointments, handle rescheduling/cancellations, and oversee patient flow
  • Manage clinic bookings via online systems, ensuring calendars are accurate and up to date
  • Deliver exceptional pre- and post-treatment patient follow-ups
  • Provide clear and accurate information regarding treatments, pricing, and aftercare
  • Organise the doctor's schedule, appointments, and daily priorities
  • Assist with personal errands, administrative tasks, and travel arrangements
  • Support during consultations, including note taking and managing patient photos where required
  • Monitor stock levels for products, disposables, and PPE, placing orders when needed
  • Maintain a clean, organised, and welcoming clinic environment
  • Prepare and reset treatment rooms before and after each appointment

Requirements:

  • Bachelor's degree or equivalent (essential)
  • Strong verbal and written communication skills
  • Confident using WhatsApp, social media, email platforms, booking systems, and Microsoft Office
  • Calm, friendly demeanour with excellent multitasking abilities
  • Highly trustworthy, discreet, and comfortable handling sensitive medical information
  • A proactive, "can-do" attitude with a willingness to pitch in wherever needed
  • 1-2 years in a similar role (medical or aesthetic clinic experience preferred)

Nice to have:

medical or aesthetic clinic experience

Additional Information:

Job Posted:
February 05, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:

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

Briefcase Icon

Similar Jobs for Junior Clinic Manager

Junior Clinical Trial Manager

At Parexel FSP people make the difference. We have a crucial mission: to prevent...
Location
Location
Spain
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Strong experience in clinical trial documentation and processes (e.g., protocols, CRFs, monitoring plans)
  • Strong experience as CRA and Lead CRA
  • Strong experience of data management and query resolution in clinical trials
  • Overall knowledge of site management and monitoring procedures
  • Good Clinical Practices (GCPs) and regulatory compliance (FDA and ICH guidelines)
  • Degree in the life sciences field preferred
Job Responsibility
Job Responsibility
  • Manage external vendors and contract research organizations
  • Prepare study documents such as the Monitoring Manual, Study Operations Manual, Source Data Verification Plan and Laboratory Manual
  • Coordinate and be responsible for the design of study materials such as CRFs, patient diaries, study participation cards and source documents
  • Assist with protocol development and study report completion
  • Manage monitoring activities (may include routine on-site clinical monitoring) at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs and study protocols
  • Provide guidance, direction, and management to CRAs
  • Track patient enrollment
  • qualify, initiate, monitor, perform closeout activities, and review site reports
  • and assist in coordination of data management activities
  • Coordinate study supplies
What we offer
What we offer
  • Exceptional financial rewards, training, and development
  • Healthy work-life balance
Read More
Arrow Right

Senior Clinical Trial Assistant

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
United States of America
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in a relevant field such as life sciences, healthcare administration, or clinical research highly preferred
  • Experience in clinical research, site management, or monitoring, with a solid understanding of clinical trial processes and GCP guidelines
  • Strong organizational and project management skills, with the ability to handle multiple priorities and deadlines
  • Excellent analytical skills and attention to detail, with a focus on maintaining high-quality standards
  • Exceptional communication and interpersonal skills, with the ability to build and maintain effective relationships with site personnel and cross-functional teams
Job Responsibility
Job Responsibility
  • Coordinating monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues
  • Assisting in the preparation and review of regulatory documents, ensuring all site activities are compliant with GCP and applicable regulations
  • Collaborating with cross-functional teams to facilitate effective communication and support for trial sites throughout the study lifecycle
  • Tracking site performance metrics, analyzing data, and providing reports to enhance site management efficiency
  • Participating in training initiatives and mentoring junior staff to support their development in clinical trial management
What we offer
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
Read More
Arrow Right

Senior Site Management Associate

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
Romania , Bucharest
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in life sciences, clinical research, or a related field
  • Extensive experience in site management, clinical operations, or monitoring within the clinical research industry
  • Strong understanding of clinical trial processes, Good Clinical Practice (GCP), and regulatory requirements
  • Excellent problem-solving and organizational skills, with the ability to manage multiple sites and timelines
  • Effective communication and interpersonal skills, with a focus on collaboration and maintaining strong site relationships
  • Romanian language is required
  • Italian language is strong preference
Job Responsibility
Job Responsibility
  • Overseeing day-to-day site management activities, ensuring that clinical trial sites comply with study protocols, regulatory requirements, and timelines
  • Collaborating with site staff and cross-functional teams to resolve issues, monitor progress, and ensure timely data collection and reporting
  • Assisting with site initiation, monitoring visits, and close-out activities to ensure the proper execution of clinical trials
  • Providing guidance and mentorship to junior site management staff, fostering collaboration and process improvement
  • Preparing and maintaining site management documentation, including site reports, communications, and updates on site performance
What we offer
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
Read More
Arrow Right

Senior Clinical Trial Manager

At Hemab you will join a clinical-stage biotech company on an exciting journey t...
Location
Location
Denmark , København og omegn
Salary
Salary:
Not provided
life-science-talent-solutions.dk Logo
Life Science Talent
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s Degree in life sciences or healthcare discipline
  • At least 5-7 years of clinical trial management experience and at least 2 years of clinical monitoring experience in the biotech/pharmaceutical industry
  • Proven experience managing Phase 3 clinical trials from initiation through completion
  • Direct experience conducting global/multinational clinical trials across multiple geographic regions (US, EU, MENA, Asia-Pacific preferred)
  • Experience in rare disease or orphan drug development, with demonstrated understanding of unique challenges in patient recruitment, regulatory pathways, and engagement with specialized centers
  • Working knowledge of ICH/GCP regulations and guidelines
  • Solid understanding of cross-functional areas, including data management/biostatistics, regulatory affairs, and pharmacovigilance
  • Proven verbal and written communication skills
  • enjoys interacting with others regularly
  • Able to prioritize tasks and work independently
Job Responsibility
Job Responsibility
  • Manage CRO study team(s), clinical sites, laboratory vendor(s), and other outsourced work on assigned studies to ensure consistency of methods, interpretation, and approach with other Hemab-sponsored studies
  • Lead global clinical trial execution across multiple regions and countries, ensuring coordination of multinational study teams and compliance with regional regulatory requirements
  • Lead in the development and review of protocols, study budgets, investigator brochures, clinical study reports, and other clinical documents and regulatory filings as needed
  • Implement study startup activities, including the development of informed consent forms, study training materials, manuals, plans, and study tools for assigned study
  • Oversee regulatory/ethics submissions
  • Effectively evaluating qualified study sites, oversee monitoring activities, and support clinical site initiation visits, co-monitoring, and close-out visits as needed
  • Oversee day to day study conduct
  • including management of operation questions from CRO and sites, tracking subject recruitment, laboratory samples, and review of monitoring reports
  • responsible for study close-out activities
  • Assess study drug requirements and shipment and supply logistics, contributing to pharmacy manual
  • Fulltime
Read More
Arrow Right

Clinical Negligence Senior Associate

This is an opportunity to be part of a Legal 500 ranking team that offers top qu...
Location
Location
United Kingdom , Manchester
Salary
Salary:
61000.00 - 68000.00 GBP / Year
https://www.douglas-scott.co.uk Logo
Douglas Scott
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • strong experience of managing high value, defendant Clinical Negligence cases to include litigation
Job Responsibility
Job Responsibility
  • managing a complex caseload of high value, catastrophic Clinical Negligence cases
  • supervising and developing more junior lawyers in the department
What we offer
What we offer
  • Flexible/hybrid working
  • Private medical cover
  • Buy and sell holidays
  • Enhanced parental leave
  • Pension scheme
  • Fulltime
Read More
Arrow Right

Regulatory Writing Senior Manager

In this key role you will serve as the functional area lead on product teams, le...
Location
Location
United States
Salary
Salary:
152684.00 - 193308.00 USD / Year
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Doctorate degree and 2 years of directly related experience
  • Master’s degree and 6 years of directly related experience
  • Bachelor’s degree and 8 years of directly related experience
  • Associate’s degree and 10 years of directly related experience
  • High school diploma / GED and 12 years of directly related experience
  • Experience with regulatory documents in Regulatory Affairs, Research, Development or related area
  • 5+ years of experience in medical writing in the Biotech/Pharmaceutical industry
Job Responsibility
Job Responsibility
  • Author or oversee the authoring of all regulatory submission documents including Clinical Study Reports, Investigator Brochures, Responses to Questions, Protocols, Protocol Amendments, Informed Consent Forms, Table of All Studies, Clinical Overview Addenda, eCTD Module 2 Clinical Summary Documents, Briefing Documents, and Pediatric Investigation Plans
  • Conduct the formal review and approval of authored documents, following applicable standard operating procedures
  • With limited supervision, lead regulatory writing activities for complex product submissions, including new and supplemental drug applications/biologics license applications
  • Serve as functional area lead on product teams (e.g., Global Regulatory Team, Evidence Generation Team, Global Safety Team, Label Working Group)
  • Provide functional area input for Global Regulatory Plan and team goals
  • Supervise the work of contract and freelance writers and mentor junior medical writers as assigned
  • Lead departmental and cross-departmental initiatives, as appropriate
  • Generate document timelines
What we offer
What we offer
  • Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans and bi-annual company-wide shutdowns
  • Flexible work models, including remote work arrangements, where possible
  • Fulltime
Read More
Arrow Right
New

Manager, Clinical Data Management

The Manager – Clinical Data Management (CDM) is a senior functional expert in Cl...
Location
Location
Italy , Milano
Salary
Salary:
Not provided
it.alfasigma.com Logo
Alfasigma
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum of 7 years of experience in Clinical Data Management within pharma, biotech, CRO, or academic settings
  • Bachelor’s degree in life sciences, health informatics, pharmacy, computer science, or a related field
  • Strong understanding of clinical trial processes and data management principles
  • Experience with EDC systems (e.g., Medidata Rave, Veeva EDC)
  • Expertise in eCOA and RTSM systems
  • Familiarity with data visualization tools
  • Proficiency in statistical software (e.g., SAS)
  • Knowledge of regulatory requirements and CDISC standards
  • Strong organizational and communication skills
  • High attention to detail
Job Responsibility
Job Responsibility
  • Providing data management expertise during protocol development and amendments
  • Contributing to the selection of CROs and specialized vendors for data collection and management
  • Supporting the preparation and review of RFPs related to data management services and costs
  • Acting as the primary point of contact for CROs and vendors, ensuring high-quality deliverables within agreed timelines and budget
  • Ensuring compliance with company processes, ICH E6 guidelines, and applicable regulations
  • Collaborating on study timelines from start-up through close-out
  • Supporting the development, review, and testing of data collection tools (e.g., eCRFs, eCOA systems)
  • Contributing to the creation and maintenance of data management documentation (e.g., DMPs, Edit Check Specifications, Data Validation Plans)
  • Overseeing outsourced data management activities, including data cleaning, coding, and reconciliation
  • Maintaining oversight documentation and coordinating internal data quality reviews
What we offer
What we offer
  • Competitive salary
  • Comprehensive benefits
  • Extensive opportunities for professional growth and development
Read More
Arrow Right

Manager, Engagement

FormularyDecisions® is a digital platform connecting biopharma companies to thei...
Location
Location
United States , Remote
Salary
Salary:
Not provided
cencora.com Logo
Cencora
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum of a bachelor’s degree (in Health Economics, Pharmacy Administration, Biostatistics, Health Services Research, Clinical Epidemiology, Public Health Policy, or relevant field) or six (6) years of equivalent related experience
  • Minimum of 3 years of experience, preferably in a US managed care organization or related companies, with experience in formulary management services
  • Leadership experience or desire for management responsibilities long-term
  • Ability to think strategically and tactically
  • Ability to work well in a dynamic, successful consulting firm
  • Superior interpersonal skills, strong project management abilities, and effective analytical skills
  • Excellent writing skills and the ability to communicate complex material
  • Proficiency in utilizing Microsoft Office applications (Excel, Word, and PowerPoint)
  • Customer centric mind set
  • Supports a learning culture of continuous improvement
Job Responsibility
Job Responsibility
  • Lead clinical content strategy, development, execution, and ongoing management, including third-party content integration
  • Curate clinical and economic content through eNewsletter dissemination
  • Provide leadership in developing, testing, and presenting recruitment and engagement strategies among key market segments
  • Develop, actively monitor, report, and present recruitment and engagement metrics
  • Lead conference planning and execution for FormularyDecisions team
  • Develop and collaboratively support creation of marketing collateral and deliver/participate in virtual demonstrations
  • Manage, guide, and engage key market segments by conducting market research
  • Support business development efforts including lead generation, conference participation, and research and dissemination
  • Mentor and train junior team members in clinical and managed care concepts
  • Perform other work-related duties as assigned
What we offer
What we offer
  • Medical, dental, and vision care
  • Comprehensive suite of benefits focusing on physical, emotional, financial, and social aspects of wellness
  • Support for working families (backup dependent care, adoption assistance, infertility coverage, family building support)
  • Behavioral health solutions
  • Paid parental leave
  • Paid caregiver leave
  • Training programs
  • Professional development resources
  • Opportunities to participate in mentorship programs, employee resource groups, volunteer activities
  • Fulltime
Read More
Arrow Right