Clinical Study Coordinator, Varnamo Sweden

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Job Details

Description:

Job Title: Clinical Study Coordinator

Location: Varnamo, Sweden

Schedule: Freelance

TalentSource Life Sciences is currently searching for an experienced freelance Clinical Study Coordinator to join one of our partner companies - a leading international pharma company - in Varnamo, Sweden.

This will be a site-based position on an ad-hoc basis and the successful candidate will be working on studies dedicated to one client.
We will require the Coordinator to work one block of three consecutive days at site, two times per year. There will be periods of several months with no activities.

As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client counter-parts.

TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having continuous support from your TalentSource Line Manager.

Main Responsibilities:

• Support clinical research teams with ongoing conduct of studies
• Assist project teams with study specific documentation (completion of CRFs/eCRFs and Data Clarification Forms, maintain drug accountability records, complete site status reports)
• Ensure assessment and signature of documents by the PI
• Have an up to date knowledge of ICH-GCP, appropriate regulations and the company's SOPs
• Work with the Clinical Research Associate and attend site visits
• Assist in the preparation, handling and tracking of Ethics/Regulatory submissions
• Maintain the study files and databases for the project
• Coordinate ordering, dispatch and tracking of trial materials
• Assist project teams with trial progress tracking by updating the Clinical Trial Management systems
• Assist in the tracking and distribution of safety reports
• Coordinate document translations
• Assist in the preparation of presentations
• Train subjects to use IMP device and the e-diary
• Attend Investigator Meeting and Site Initiation Visits
• Discuss Informed Consent Forms (ICF) with trial subjects
• Assist the Principal Investigator in determining subject eligibility
• Serious Adverse Event (SAE) reporting transmission through safety gateway
• Receipt/storage of Investigational Product (IP) and dispensation of IP via IXRS
• Communicate with Institutional Review Board (IRB) and Institutional Ethics Committee (IEC)
• Maintain documentation in Investigator Site File

Requirements

• Bachelor's degree in a scientific or related field
• IATA certification would be beneficial
• Previous experience in a similar role as a Project Assistant, Clinical Trial Assistant, Study Coordinator or similar
• Experience training patients
• Good knowledge of GCP
• Possesses good communication and organizational skills

If you have the experience and are interested in discussing the role for this position, please contact Laura Guascone, Consultant, TalentSource Life Sciences Unit at laura.guascone@cromsource.com .

Why choose TalentSource Life Sciences/CROMSOURCE?

CROMSOURCE is a family owned international, full-service Contract Research Organization who, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. TalentSource Life Sciences is a fully dedicated flexible resourcing unit within CROMSOURCE and the successful growth has been achieved by putting high quality and client focus at the heart of everything we do.

Our employees are the most valuable company asset and we value resources and ensure they work in a friendly, family environment and develop their skills and talents. Human Resources is the fulcrum around which all activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel clear tools to manage both internal and client processes with the same methodology.

Our approach is to equally value our clients and our own people. We know that we are not simply providing 'staff' or 'resources'. We are providing expert people. Highly talented, well trained, motivated people who make a positive difference to the work of our clients every day. Together we help our clients succeed in their work developing medicines and medical devices for patients around the world. Our large management team consists of a people with an extended experience within pharma and a high level of market knowledge.

CROMSOURCE comes from the merger of MSOURCE and CROM in 2011 and we are great at recruitment and staffing services! We're proud to partner with the industry's leading Pharmaceutical, Biotechnology, Medical Device and Marketing Communications worldwide, securing great global talent. We our open, friendly and approachable and aim to support you through the recruitment process every step of the way.

For the client client-facing positions, the successful candidates must be confident and be able to drive the role and themselves and to work autonomously in close liaison with a line manager at TalentSource, who will provide you with mentoring and guidance. Most of our roles are permanent positions with Cromsource and you will be working on studies for just one client.

How can we help you on your next career move? Learn more on LinkedIn, YouTube, Facebook, Twitter, and Glassdoor.

Key words:

Study Coordinator, Clinical Coordinator, Research Coordinator, Trial Coordinator, Clinical Research Associate, CRA, Freelance CRA, Freelance, Freelancer, Contract, CRO, Contract Research Organization, Outsourced, Pharmaceutical, Consultant

Skills: Clinical Trial Coordinator Location: Varnamo, Sweden Share:
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Company

ClinChoice is a recognized and highly respected mid-size, global, full-service contract research organization (CRO) specializing in clinical development, post-marketing, and functional service support. We provide comprehensive end-to-end solutions, taking products from early clinical development to post-approval lifecycle management. We are committed to fostering innovation in the pharmaceutical, biotechnology, medical device & diagnostics, consumer health, cosmetics, and nutraceuticals industries. Since our establishment in 1995, we have consistently delivered high-quality services and solutions throughout the entire development lifecycle of our clients’ products. We serve a wide-ranging clientele that encompasses six of the top ten pharmaceutical companies, leading medical device companies, preeminent biotechnology companies, the largest consumer health and cosmetics companies, and numerous small-to-mid-sized innovator companies. With over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific, we are positioned to fulfil our clients’ needs locally and globally.

We’re on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.

Company info

Website
Telephone
+44 1628 566121
Location
Suite G48
268 Bath Road
Slough
Berkshire
SL1 4DX
United Kingdom
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