Travel and Customer Service Coordinator (Canada)

Posted 12 Days Ago
Hiring Remotely in Canada
Remote
1-3 Years Experience
Consulting
The Role
Key contact for trial participants regarding travel and logistical details for clinical trials. Responsible for managing participant communications, travel budget, and supporting clinical trial Project Managers. French-Canadian language proficiency required.
Summary Generated by Built In

Clincierge, a Greenphire company, is on a mission to support patients in clinical trials worldwide. The key to our success is our collaborative and innovative environment. We are always looking for new ways to invent solutions to ensure the clinical trial process is easier with personalized concierge services.

Our patients come from all walks of life, and so do we. We hire great people from a wide variety of backgrounds, not just because it’s the right thing to do, but because we recognize that it is the unique contributions of our people that drives our success.

The Coordinator is the key point of contact for participant communications in the management of all participant travel, logistical details, and expense reimbursements for clinical trials. The coordinator is responsible for supporting the team of clinical trial Project Managers by participant tracking and record keeping.

Please note: This is a contract-position. It is part-time, 2-20 hours per week, and pays on an hourly basis. Hours are not guaranteed.

Responsibilities

  • Key contact for trial participants regarding ground transportation, air travel and hotel accommodations
  • Manages travel and transportation budget for trial participants
  • Participates in discussions with vendors and internal team members regarding trial participant requirements
  • Supports hospital or clinical staff relating to trial participant enrollments and visit schedules
  • Promptly responds to all inquiries of the trial participants and hospital/clinical staff
  • Contributes to managing projects to profitable level through efficient work process

Requirements:

  • Bachelor’s Degree or equivalent work experience
  • French-Canadian language required
  • Minimum 2 years of travel industry, customer service or pharma industry experience required
  • Excellent working knowledge of Microsoft Suite
  • Knowledge of Smartsheet and SharePoint preferred
  • Ability to learn new procedures quickly and efficiently
  • Highly organized and plan-oriented; adept at prioritization and follow-up
  • Excels in cross-departmental communication
  • Confidence and follow through in decision-making

Working Environment:

  • Work environment is from a home office with personal computer and telephone  
  • The position requires flexible work hours, both traditional and non-traditional  
The Company
HQ: Philadelphia, PA
90 Employees
Hybrid Workplace
Year Founded: 2014

What We Do

Improve your clinical trial performance.


Clincierge™ enables patients to connect more effectively with clinical trials of new medicines. We reduce barriers to trial participation, making it possible for patients and others to gain faster access to potentially useful new treatments.

Our unique services – including individualized travel and housing logistics, payment/reimbursement systems, and ongoing patient, family, and caregiver support – reduce the anxiety and out-of-pocket expense that patients and their families too often face when participating in clinical trials. We address special patient needs and the demands that complex trial designs place on them and their families, building custom solutions to specific study-related problems as required. From the time a patient enrolls in a Clincierge-supported study until its completion, our multi-lingual, in-country Clincierge Coordinators provide seamless, personalized support for patients, their families, and caregivers, communicating closely with them each step of the way.

By helping patients, we help trial sponsors, CROs, and research institutions manage the cost and time of clinical trials. Clincierge’s value-added services not only enhance patient recruitment and improve retention, they also relieve clinical research associates, clinical investigators, and other study sponsors and trial site personnel from time-consuming patient logistics. Our services enable study staff to prioritize patient care and focus on study outcomes. We reduce clinical trial administrative costs and streamline patient payments and reimbursements through our efficient online portal.

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