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Clinical Research Coordinator

  • Company: Healthcare Professionals Group
  • Location: Botany, Botany Bay
  • Salary: Pay not listed
  • Full Time
  • Company site
  • Pay not listed

Healthcare Professionals Group at a glance

Clinical Research Coordinator at Healthcare Professionals Group in Botany, Botany Bay

Position Summary

The Clinical Research Coordinator position at Healthcare Professionals Group offers a unique opportunity to be part of a diverse and dynamic clinical research organization. This role involves taking ownership of study activities within a varied portfolio of clinical trials, collaborating with experienced professionals, and expanding your therapeutic area expertise.

Core Duties

  • Taking ownership of study activities from start to finish
  • Collaborating with experienced research professionals
  • Expanding therapeutic area experience through diverse studies
  • Ensuring compliance and adherence to clinical trial protocols
  • Managing participant data and ensuring accurate documentation
  • Participating in regular team meetings and training sessions

Who We're Looking For

We are seeking a motivated Clinical Research Coordinator with a strong background in clinical research, excellent organizational skills, and the ability to work effectively within a team. A bachelor's degree in a relevant field is preferred, along with previous experience in a similar role.

Why Join Healthcare Professionals Group

Joining Healthcare Professionals Group means becoming part of an organization that values participant excellence and has a strong reputation for conducting high-quality clinical trials. You will have the opportunity to be exposed to a diverse portfolio of studies, take ownership of study activities, and collaborate with experienced professionals in a supportive environment.

Applying for This Role

If you are passionate about contributing to medical research and expanding your expertise in clinical trials, we encourage you to apply. To join our team, please complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there.

Apply on company site

You’ll finish your application on the employer’s website. We don’t ask for a resume on this page.

What people say about Healthcare Professionals Group

Recent news

Aggregated from public discussions and news; opinions are the authors’ own.

About this role & career path

Traits that fit this role

  • Adaptability
  • Perseverance
  • Achievement Orientation
  • Cooperation
  • Intellectual Curiosity

Source: O*NET Work Styles (Distinctiveness Rank).

Typical preparation needed: Job Zone 4: Considerable Preparation Needed. Most of these occupations require a four-year bachelor's degree, but some do not. — via O*NET

Industry news

Source: O*NET (public-domain bulk data)

Salary & compensation

Workers in Management occupations earn a national median of $86,012via US Census ACS / Data USA

Job details above are provided by the employer/source. The sections on this page are compiled from public data sources with AI assistance.

Accommodations: if you need a workplace accommodation to apply for or perform this job, see ADA.gov or EEOC.gov for guidance on your rights and how to request one.

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Listing facts

  • Role Clinical Research Coordinator
  • Employer Healthcare Professionals Group
  • Location Botany, Botany Bay
  • Type Full Time
  • Pay (from listing) Pay not listed
  • Posted August 4, 2026
  • Apply by September 3, 2026
  • Overview Full job description on this page (264 words)

Facts above come from this job record on Get A Job.AI — not copied from third-party review sites.

Typical work in Clinical Research Coordinator

Independent occupational context from O*NET (U.S. public-domain labor data). This is about the occupation, not a rewrite of this employer's posting.

  • Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
  • Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
  • Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses.
  • Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
  • Inform patients or caregivers about study aspects and outcomes to be expected.
  • Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.

Source: O*NET

Public discussions & open sources

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Cached public sources (Hacker News, Dev.to, GitHub, etc.).

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Occupation family: Clinical Research Coordinator

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Clinical Research Coordinator Healthcare Professionals Group · Botany, Botany Bay