Clinical Trial Manager (TO)

Hiring By - Biostaffic

 BioPharma

Job Highlights

Not Disclosed

Remote Job

Posted 4 months ago
Job details
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
Responsibilities:
  • Lead the planning, implementation, and execution of clinical trials in compliance with regulatory requirements and company SOPs.
  • Act as the primary point of contact for internal and external stakeholders, ensuring effective communication and collaboration throughout the trial lifecycle.
  • Manage study timelines, budgets, and resources, providing proactive solutions to challenges that may arise.
  • Oversee the selection and management of study sites, CROs, and vendors to ensure trial success.
  • Monitor trial progress, identify potential risks, and implement mitigation strategies to maintain study quality and timelines.
  • The CTM will also participate in Sponsor, Investigator and bid defense meetings.
Qualifications:
  • Bachelor's degree in a relevant field (Life Sciences, Nursing, or equivalent).
  • Extensive experience in clinical trial management, demonstrating a successful track record in the pharmaceutical or CRO industry.
  • Strong leadership, organizational, and problem-solving skills.
  • Thorough knowledge of ICH-GCP guidelines and local regulatory requirements.
  • Excellent communication and interpersonal abilities, with a proven capacity to manage multiple stakeholders effectively.
Why Join ICON?
  • Be part of a global leader in clinical research, contributing to groundbreaking advancements in healthcare.
  • Collaborative work environment with ample opportunities for professional growth and development.
  • Competitive compensation and benefits package.
  • Contribute to innovative research and make a tangible impact on patient well-being.
Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

Benefits Offered?

  • No

Bonus Offered?

  • No

Travel Required?

  • No

Remote Job:

  • Yes

Global Experience Needed?

  • No

Specialized Experience Needed?

  • No

Apply before:

  • Apr 15, 2024
Company Overview
ICON Plc
ICON Plc

Current Openings: 0

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
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