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Parexel Hiring Freshers for Patient Concierge Associate

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Parexel

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Biotechnology , Nursing , Healthcare Administration

Hyderabad

Freshers

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Parexel, one of the world’s leading clinical research organizations (CROs), has announced a new opening for the position of Patient Concierge Associate. This is an excellent opportunity for fresh graduates and candidates with up to two years of experience who want to build a career in clinical research operations, patient services, and clinical trial support.

The role is based in Remote – Hyderabad, India, offering candidates the chance to work with global clinical trial teams while supporting patient travel, reimbursement, and operational coordination activities.

If you are looking for a Parexel Patient Concierge Associate job, clinical research jobs for freshers, or healthcare administration jobs in Hyderabad, this opportunity could be an excellent career move.


Job Details

ParticularDetails
CompanyParexel
PositionPatient Concierge Associate
Job TypeFull-Time
Experience0โ€“2 Years
QualificationBachelor’s Degree Preferred
LocationHyderabad, India (Remote)
DepartmentPatient Services / Clinical Operations
Posted On26 June 2026

About Parexel

Parexel is a globally recognized Contract Research Organization (CRO) providing clinical development, regulatory consulting, market access, and patient-focused solutions. The company partners with pharmaceutical, biotechnology, and medical device organizations to accelerate the development of innovative therapies that improve patient health worldwide.


Key Responsibilities

As a Patient Concierge Associate, you will support patient travel and reimbursement programs for clinical studies by performing various administrative and operational tasks.

Responsibilities include:

  • Monitor and manage shared project mailboxes
  • Route requests to appropriate internal teams
  • Maintain project trackers and documentation
  • Update SharePoint records and Excel reports
  • Support study startup documentation
  • Coordinate meetings and prepare meeting notes
  • Track onboarding activities
  • Communicate with vendors regarding project documentation
  • Maintain accurate study records
  • Prepare routine reports and presentations
  • Assist with invoice processing and financial tracking
  • Ensure compliance with SOPs and internal procedures
  • Support daily project coordination activities

– Serve as primary liaison with patient concierge vendors. Conduct status calls, review documentation, ensure regulatory compliance, and manage vendor performance across multiple trials.
– Develop communication materials and training resources for study teams. Provide guidance on country-specific requirements and vendor selection.
– Review Informed Consent Forms for alignment with patient concierge services. Manage regulatory requirements, track approvals and site activation, and ensure protocol compliance.
– Monitor budgets, track invoices, and manage out-of-scope requests.
– Analyze vendor metrics and prepare status reports for sponsors. Track site onboarding, service utilization, and document best practices for continuous improvement.


Required Qualifications

Candidates should possess:

  • Bachelor’s Degree (Preferred)
  • 0โ€“2 years of administrative or coordination experience
  • Healthcare or Clinical Research exposure is an advantage
  • Strong MS Office skills (Excel, Word, Outlook, PowerPoint)
  • Good communication skills
  • Strong organizational abilities
  • Attention to detail
  • Ability to multitask effectively
  • Teamwork and collaboration skills
  • Willingness to learn and grow

Preferred Skills

  • Clinical Trial Administration
  • Patient Support Services
  • Documentation Management
  • SharePoint
  • Microsoft Excel
  • Calendar Management
  • Vendor Coordination
  • Administrative Support
  • Project Coordination
  • Clinical Operations

Why Join Parexel?

Working at Parexel offers several advantages:

  • Opportunity to work with a leading global CRO
  • Exposure to international clinical trials
  • Career growth in Clinical Research
  • Collaborative work culture
  • Professional learning opportunities
  • Patient-focused work environment
  • Global project experience
  • Competitive compensation and benefits

Who Should Apply?

This opportunity is suitable for:

  • B.Pharm Graduates
  • Pharm.D Graduates
  • Life Science Graduates
  • Biotechnology Graduates
  • Nursing Graduates
  • Healthcare Administration Graduates
  • Freshers looking for Clinical Research jobs
  • Candidates with up to 2 years of experience

How to Apply

Application Link

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