JUMP TO CONTENT

Study Start Up Associate I, Taipei

049195_2

About the role

This vacancy has now expired. Please see similar roles below...

"At ICON, it's our People that set us Apart"
 
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries.
 
As a SSU you will be responsible for the independent preparation, review and approval of country related submission packages in accordance with ICH, GCP and all applicable regulations, laws and other guidelines and ethical standards. Developing and finalizing Master and Country Specific Information Sheets/Informed Consent Forms (SIS/ICFs)
  
Role Summary;
Serving as a primary contact for investigators and research coordinators, you will perform feasibility, site identification, site contract negotiation and other assigned study startup activities. This will include the preparation, review and approval of country related ethics/regulatory submission packages and site level critical documents for Investigational Product (IP) release. Some travel is anticipated, to attend Kick-Off, Investigator and/or study team meetings.
 
Job Description;
  • Perform feasibility, site identification, site contract negotiation, and other study start up activities, as assigned
  • Provide country specific Study Start Up expertise to Study Start Up Team Leads and project teams.
  • Responsible for the preparation and coordination of submissions to ethics and other bodies
  • Develop, finalize and review Master and Country Specific Subject Information Sheets/Informed Consent Forms (SIS/ICFs)
  • Responsible for the timely and accurate data entry of all relevant Study Start Up activities into the appropriate clinical trial management system in assigned countries Responsible for the collection and maintenance of the current Ethics Committee (EC) submission information, and similar information for other related.
  • Develop and maintain effective relationships with local, regional and country authorities
  • Travel(approximately 15%) domestic and/or international.   Anticipated activities may include attendance at Bid Defences, Kick-Off, Investigator or study team meetings.
 Requirements;
  • Knowledge and experience in the clinical study start up requirements and activities for all assigned countries (or the ability to find this out for new countries)
  • Good organizational skills and the ability to manage multiple tasks
  • An excellent level and proven experience high standards of attention to detail
  • Good written and verbal communication skills. Proficient in English and local language required for country assignments
  • Ability to liaise with colleagues from Study Start Up, other departments and clients, if required
  • Strong project management skills
  • Highly developed problem solving skills
  • Customer service focused
  • Solution-focused
  • Bachelor’s degree or local equivalent and/or with appropriate experience from the Medical/science background and/or discipline

Compared with our competitor and pharmaceutical companies, we provide more flexible and reasonable working platform for coach and educate the new comer to be a professional person to concentrate on relevant industry. ICON also provides the good package and benefit to adapt the marketing development.

 
What’s Next
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity. ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment
List #1

Day in the life

Endometriosis yellow ribbon
Shining a Light on Endometriosis Awareness Month

Teaser label

Inside ICON

Content type

Blogs

Publish date

04/18/2024

Summary

Endometriosis Awareness: A Vital Cause In March, ICON, through its Networking Organization for Women (NOW) employee resource group, joined the global effort to raise awareness about endometriosis

Teaser label

Endometriosis Awareness Month sheds light on this often-misunderstood condition affecting millions worldwide.

Read more
Data visualisation
The Role of Data Management in Clinical Trials

Teaser label

Industry

Content type

Blogs

Publish date

04/18/2024

Summary

Introduction to Data Management in Clinical Trials In the field of clinical research, data management plays a crucial role in ensuring the success and accuracy of clinical trials. Clinical trials

Teaser label

This blog examines the critical role of data management in clinical trials.

Read more
Medicine on a shelf
Navigating the Clinical Research Supply Chain

Teaser label

Industry

Content type

Blogs

Publish date

04/12/2024

Summary

Introduction to the Clinical Research Supply Chain The clinical research supply chain plays a crucial role in the successful execution of clinical trials. It encompasses a complex network of activ

Teaser label

Discover the intricate workings of the clinical research supply chain in this comprehensive guide.

Read more
View all

Who we are

Press play to find out more

Similar jobs at ICON

Clinical Associate

Salary

Location

Spain, Barcelona

Location

Barcelona

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Operations

Job Type

Permanent

Description

• Recognize, exemplify and adhere to ICON's values which center around our culture of accountability, integrity, partnership, collaboration and excellence in delivery. • As a member of staff, the empl

Reference

JR119238

Expiry date

01/01/0001

Lourdes Roy Prats Read more Shortlist Save this role
Senior Site Management Associate - multilingual skills

Salary

Location

Poland, Warsaw

Department

Full Service - Development & Commercialisation Solutions

Location

Sofia

Warsaw

Barcelona

Madrid

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

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 I

Reference

JR117450

Expiry date

01/01/0001

Magda Kozuszek Read more Shortlist Save this role
Senior Pharmacovigilance Associate

Salary

Location

India, Chennai

Location

Chennai

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Drug Safety

Job Type

Permanent

Description

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 I

Reference

JR116173

Expiry date

01/01/0001

Archana Bakkiyarajan Read more Shortlist Save this role
Senior Project Manager

Salary

Location

Belgium

Department

Clinical Trial Management

Location

Belgium

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us

Reference

2024-109205

Expiry date

01/01/0001

Tanzina Guerni Read more Shortlist Save this role
RWE Statistical Programmer

Salary

Location

United States

Department

Biometrics Roles

Location

United States

Business Area

ICON Strategic Solutions

Job Categories

Statistics

Job Type

Permanent

Description

The study programmer position will be responsible for manipulating large databases and generating reports to enable analysts to explore real world healthcare data assets. 

Reference

2024-110035

Expiry date

01/01/0001

Jamie Pruitt

Author

Jamie Pruitt
Read more Shortlist Save this role
RWE Statistical Programmer

Salary

Location

United States

Department

Biometrics Roles

Location

United States

Business Area

ICON Strategic Solutions

Job Categories

Statistics

Job Type

Permanent

Description

The study programmer position will be responsible for manipulating large databases and generating reports to enable analysts to explore real world healthcare data assets. 

Reference

2024-110034

Expiry date

01/01/0001

Jamie Pruitt

Author

Jamie Pruitt
Read more Shortlist Save this role

Browse popular job categories below or search all jobs above