Clinical Research Associate- Home Based- Multiple locations Available!
ICON Clinical Research - North Wales, PA

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Description

Clinical Research Associate

This is an opportunity to work for ICON’s Late Phase and Outcome Research division (LPOR). With a track record for successful analysis and extensive scientific publication, the ICON Late Phase & Outcomes Research division delivers high-impact evidence that explores and demonstrates the value of pharmaceutical, biotechnology, consumer healthcare and medical device products in all global markets, with a focus on maximising return on investment.

Our global team of experts provide a full spectrum of market-leading clinical Late Phase research, real-world studies, health economics and patient reported outcomes to support our clients’ product lifecycle, from early stage development, pricing and market access strategies, through regulatory and reimbursement approvals, labeling claims, and in-market support.

We now seek to recruit a dedicated, hardworking Clinical Research Associate, to join our busy European team.

Overview of the role

Working independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested.

Managing sponsor generated queries efficiently and taking responsibility for study cost effectiveness; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.

Depending on your level of experience, you may assist in training and mentoring less experienced CRA’s and/or manage CRA’s working on international projects.

Role Requirements

With a University degree in medicine, science, or equivalent; you will have previous monitoring experience in medium sized studies, including study start-up and close-out (for all roles above Entry Level). You should also have knowledge of ICG GCP guidelines and the expertise to review and evaluate medical data.

Fluent in English, as well as the local language, you will possess excellent written and verbal communication and interpersonal skills enabling you to deal with queries in a timely manner. You should be able to produce accurate work to tight deadlines within a pressurised environment.

You must be available to travel at least 50% of the time (international and domestic -fly and drive) and should possess a valid driving licence.

You will have the opportunity to progress your career and may wish to move into Project Management or into other related areas where you can further develop your skill set.

Benefits of Working in ICON

Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package. 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.

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Job

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Clinical Research Associate

Primary Location

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US-North Wales

Organization

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Clinical - CRA Management

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Job Posting

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16/Oct/13, 7:25:01 PM

ICON Clinical Research - 10 months ago - save job - block
About this company
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Contract research organization (CRO) ICON is not iconic yet, but it would like to be. By the time a new drug hits the market, it has passed...