Study Start Up Associate job in

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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 Also responsible for the independent preparation, review and approval of site level critical documents for Investigational Product (IP) release in accordance with regulatory/sponsor requirements – within specific timelines and quality standards. Developing and finalizing Master and Country Specific Information Sheets/Informed Consent Forms (SIS/ICFs)

Overview of the role

As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
Travel (approximately 15%) domestic and/or international. Anticipated activities may include attendance at Kick-Off, Investigator or study team meetings
Perform feasibility, site identification, site contract negotiation, and other study start up activities, as assigned
Prepare, review and submit submissions to CA, EC and other relevant authorities in order to obtain all necessary authorizations/approvals pertaining to the clinical trial conduct.
This includes, but it is not limited to:

ethics/regulatory/other relevant authority approvals for clinical trials
ethics/regulatory/other relevant authority approvals for trial amendments
ethics/regulatory/other relevant authority study notifications
authorizations for import/export of investigational products, clinical supplies and biological samples
approvals from the national authorities for data protection

Review and translate Drug Labels
Advise Sponsor on knowledge content for development of Drug Labels
Perform independent quality review of submission package
Responsible for the collection and maintenance of the current Regulatory/Competent Authority (CA) and Ethics Committee (EC) submission information, and similar information for other related organizations, for the assigned countries and update relevant ICON information system
Responsible for the translation and co-ordination of translations for documents required for submission
Perform timely and accurate data entry of regulatory documents, submission status and maintenance of Country/Investigator information in the appropriate clinical trial management system
Copy and route incoming correspondence, internal documentation, etc., as appropriate
Responsible for the collection of critical documents required for IP Release
Attend study team meetings as required (maybe discretionary), including Kick-Off Meetings which are mandatory
Assemble and distribute study materials to Clinical and Project teams, including materials to study sites and Investigator Meetings (e.g.; investigator binders) and vendors, as appropriate
To be familiar with ICH GCP, relevant country regulations/guidelines and ICON SOPs
Competent in communication skills for timely follow-up, issue resolution and report updates; as outlined in the communication and escalation plan with timely documentation

Role Requirements

Bachelor’s Degree or local equivalent and/or appropriate experience from the Medical/science background and/or discipline
Previous relevant experience
Experience and/or understanding of clinical study start up requirements and activities
An excellent level and proven experience high standards of attention to detail
Excellent written and spoken English
Competent computer skills
Due to the nature of this position it may be required for the employee to travel. Therefore, dependent on the employee’s location, the employee may be required to possess a valid Driver’s license

Benefits of Working in ICON

Other than working with a great team of smart and energetic people, we also offer a very competitive salary and benefits package that includes an excellent pension scheme, private health care, life assurance and staff recognition schemes. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.

We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.

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.

Application process

Once you find a job opening that fits your skills and interests, you can create an account, apply and check back on the progress of your application or apply for other roles. Once your application has been received, a confirmation email will be sent to your email.

Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.

One of our experienced recruiters will read your profile and determine if you're fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.

Reasonable Accomodations

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Study Start Up Associate

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

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