Current jobs related to Study Start Up Associate I - กรงเทพมหานคร - ICON plc

  • Study Start-up Manager for Biopharma Department

    1 week ago

    กรุงเทพมหานคร, Thailand AstraZeneca Full time

    **Study Start-Up Manager** **Job Summary**: The Study Start-Up Manager (SSU Manager) is responsible at country level for managing and conducting start-up activities in compliance with the company procedures, documents, local and international guidelines such as ICH - GCP and relevant regulations. The SSU Manager will prepare, review, track and manage site...

  • Study Start-up Associate

    2 weeks ago

    กรุงเทพมหานคร, Thailand Grand Pacific CRO Full time

    About Us: The Grand Pacific CRO team has over 25 years’ experience in conducting clinical trials in the Asia Pacific region, including Australia, New Zealand and South Africa. We have continued as a leader in the industry and have expanded services to include central laboratory, site management and image reading services. We pride ourselves on meeting...

  • Senior) Clinical Research Associate

    6 days ago

    กรุงเทพมหานคร, Thailand IQVIA Full time

    As our business grows, we are looking to further strengthen our Clinical Operations team in **IQVIA Thailand** by hiring Clinical Research Associate (CRA). You will perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines,...

  • Clinical Research Associate

    1 week ago

    คลองเตย, กรุงเทพมหานคร, Thailand PRTR Full time

    Our client is a global pharmaceutical company. They are looking for a Clinical Research Associate to join their team. **Responsibilities** - Functioning as project lead for complex BE/Phase I studies and small patient PK/clinical endpoint studies. Serve as liaison between the Mylan project team (Global Pharmacology, Product Development Department Chemistry...

  • Start-up Manager

    2 weeks ago

    กรุงเทพมหานคร, Thailand Lotus Bakeries Full time

    Thailand Bangkok Are you an experienced and innovative professional seeking an exciting opportunity to shape the success of a new greenfield factory? We are currently looking for a Strategic Start-Up Manager to join our dynamic team and lead the team in establishing our cutting-edge facility. This pivotal role requires an individual with exceptional...

  • Start-up Manager

    2 weeks ago

    กรุงเทพมหานคร, Thailand Lotus Bakeries Full time

    Thailand- BangkokAre you an experienced and innovative professional seeking an exciting opportunity to shape the success of a new greenfield factory? We are currently looking for a Strategic Start-Up Manager to join our dynamic team and lead the team in establishing our cutting-edge facility. This pivotal role requires an individual with exceptional...

  • Senior Clinical Research Associate I

    2 weeks ago

    กรุงเทพมหานคร, Thailand Labcorp Full time

    The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Covance, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assures the implementation of project plans, as assigned. Function as leader for projects of limited scope, as assigned. Assume line...

  • Study Startup Associate

    2 weeks ago

    กรุงเทพมหานคร, Thailand PSI CRO Full time

    **Company Description** We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to...

  • Sma I

    4 weeks ago

    กรุงเทพมหานคร, Thailand Icon plc Full time

    **Overview**: - As a SMA I, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **Responsibilities**: **JOB PURPOSE** - Site Management Associate is responsible for end-to-end operational study delivery, with the focus on completion and maintenance of internal...

  • Clinical Research Associate I

    1 day ago

    กรุงเทพมหานคร, Thailand IQVIA Full time

    **Essential Functions** - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. - Administer protocol and related study training to assigned sites and...

Study Start Up Associate I

2 weeks ago

กรงเทพมหานคร, Thailand ICON plc Full time

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.

Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That’s our vision. We’re driven by it. And we need talented people who share it.

If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

The Role:
As a member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices.
- Coordinate, balance and facilitate activities related to the completion of Critical Document Package (CDP) and the IP release checklist (SST004-SOP-F01) in accordance with ICH GCP guidelines and all applicable regulations, laws, ethical standards, other guidelines, sponsor requirements
- Ensure that the overall process is focused on quality, efficiency and cost containment for a particular region / sub division within the CDP group, under the general mentorship of Mgr/Sr. Manager - Central Services or Designee.

What you need
- A high school diploma or local equivalent
- Bachelor’s Degree preferably in Life Sciences
- Minimum of 1 years’ experience or understanding of clinical study start up requirements and activities.
- Experience of Clinical Trial operations and meeting regulatory guidelines
- Proficient project management skills.

Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.

We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.

But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON 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.