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Clinical Trial Manager

  • Company: IRE
  • Location: Singapore (nationwide) (nationwide)
  • Salary: Pay not listed
  • Full Time
  • Company site
  • Map
  • Pay not listed

IRE at a glance

gov.ie
  • Founded 1937

SEC filings mentioning "IRE": 2,605search EDGAR

Registered as a global legal entity (LEI 875500BCLXSQ74OUK568, BE) — via GLEIF

IRE is linked to gov.ie. Available facts note a 1937 founding year. Public company detail in the listing data is otherwise thin.

Clinical Trial Manager, IRE, Singapore (nationwide) (nationwide)

The Opportunity

IRe, a global healthcare intelligence and clinical research organization dedicated to accelerating the delivery of new medicines and treatments to patients, is seeking an experienced Clinical Trial Manager for our team in Singapore (nationwide) (nationwide). This role offers the chance to contribute significantly to groundbreaking medical advancements while working within a values-driven environment that emphasizes integrity, collaboration, agility, and inclusion.

Your Responsibilities

  • Oversee clinical trials from initiation to completion, ensuring compliance with regulatory requirements and IRe's high standards of quality and safety.
  • Collaborate with cross-functional teams including medical, regulatory affairs, and site management to ensure the smooth execution of trial activities.
  • Develop and manage project timelines, budgets, and resources effectively to meet clinical trial objectives.
  • Maintain accurate documentation and records for all aspects of the clinical trials in compliance with local and international regulations.
  • Ensure adherence to Good Clinical Practice (GCP) guidelines and other relevant regulatory requirements throughout the study lifecycle.

What You Bring

  • A minimum of 5 years of experience in clinical research, preferably within a managerial role overseeing multiple trials simultaneously.
  • Strong knowledge of GCP, ICH-GCP, and local regulations governing clinical trials.
  • Excellent project management skills with the ability to prioritize tasks effectively and manage multiple projects concurrently.
  • Proven track record in leading cross-functional teams and ensuring timely delivery of high-quality deliverables.
  • Strong communication and interpersonal skills, capable of building and maintaining effective relationships with stakeholders at all levels.

Working at IRE

IRe fosters a collaborative and inclusive environment where every team member's contributions are valued. Our mission is to bring new medicines and treatments to patients faster, and we believe that our success depends on the integrity, collaboration, agility, and inclusion of all our employees.

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What people say about IRE

Recent news

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

Working in Singapore (nationwide) (nationwide)

Singapore (nationwide) is a compact island republic in Southeast Asia, just north of the equator off the Malay Peninsula, with a main island plus many smaller islets beside the Strait of Malacca.

🇸🇬 Relocation safety for Singapore (nationwide): Very Safevia Warnely, CC BY 4.0

National unemployment rate in Singapore (nationwide): 2.8%via World Bank

GDP per capita in Singapore (nationwide): $98,814via World Bank

Consumer price inflation in Singapore (nationwide): 0.9% (annual) — via World Bank

Real GDP growth in Singapore (nationwide): 5.0% (annual) — via World Bank

    About this role & career path

    The role maps to clinical research coordination (O*NET 11-9121.01), spanning subject screening, protocol procedures, AE reporting, and study documentation.

    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

    Build the skills for this role

    Build healthcare and trial literacy with free options:

    Free & low-cost learning resources

    Expect scenario questions on eligibility screening, AE escalation, protocol adherence, and how you brief patients or caregivers. Bring examples of study docs you have owned.

    Strong fit if you can run protocol workflows tightly and communicate clearly with investigators and subjects in an on-site Singapore (nationwide) Clinical Trial Manager role at IRE.

    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 Trial Manager
    • Employer IRE
    • Location Singapore (nationwide) (nationwide)
    • Type Full Time
    • Pay (from listing) Pay not listed
    • Posted August 20, 2026
    • Apply by September 19, 2026
    • Country Singapore (nationwide)
    • Overview Full job description on this page (313 words)

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

    Typical work in Clinical Trial Manager

    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

    Attributed public threads and profiles — not employee reviews or star ratings.

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

    Employer website

    gov.ie

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    Occupation family: Clinical Trial Manager

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    Clinical Trial Manager IRE · Singapore (nationwide)