Clinical Research Associate in Finland
ATLAS MEDICAL SERVICES LTD. STI.
My research opens up
new medical possibilities.
And I do it
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Clinical Research Associate in Finland
Primary Location: Finland, Remote Job ID R0000019081 Category Clinical Trials Date Posted 01/04/2024
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Success profileAbout this rolePotential career pathEmployee insightsOur teamWhy Clinical Research Associates work at ParexelLearn about our culture
Overview
As a Clinical Research Associate (CRA) at Parexel, you act as an integral part to get treatments to patients sooner. Our CRAs' priority is the safety and well-being of the patients. As you travel to investigator sites and perform your monitoring duties, we encourage you to be inquisitive, take accountability, build relationships, and act with integrity.
Join a team with a wide variety of experiences and knowledge, and work on global projects within a broad scope of therapeutic areas. We’re looking for people who want to grow personally and professionally and support their colleagues globally and cross-functionally.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
CommunicatorDetail-orientedFlexibleOrganizedProblem-solverSelf-starter
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About This Role
Parexel is currently seeking Clinical Research Associate with fluency in Finnish and conversational proficiency in Swedish to join our team in Finland.
Your time here
At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they’re set up for success. As the clinical sites’ sole point of contact, this includes addressing and resolving site issues and questions. You’ll also manage site quality and delivery from site identification through to close-out.
As a CRA, Parexel will offer you world class technology and training catered to your individual experience. You can anticipate less travel and a lower protocol load in comparison to industry peers. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research. If impact, flexibility, and career development appeal to you, Parexel could be your next home.
What You’ll Do
Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.Build relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol.Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s).Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability.Execute. Monitor the completeness and quality of Regulatory Documentation and perform site document verification.
Knowledge And Experience
Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology Excellent interpersonal, verbal and written communication skills in Finnish and good level of Swedish
Education
Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience
Parexel is proud to be a leading Clinical Research Organization with colleagues across the globe. As a member of our team, you’ll get to know your coworkers on a personal level. Have a question? A clinical research leader, project team member, technology “super user” or collaborator are a phone call away. Our clinical research teams meet regularly to have discussions in an open environment, allowing our team members to share their expertise and promote learning within the team. Management supports and encourages career growth through consistent performance discussions and evaluations. Whether your interest is to progress into a more senior level CRA role, into line management, Quality, Project Leadership or a variety of other positions, Parexel prides itself on career opportunities for our employees.
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Potential Career Path
Parexel offers various career paths and internal development programs for CRAs to advance to the next level. This could include enhancing your technical position, moving into management, or shifting to other areas of the business.
APEX CRA CRA I CRA II Senior CRA Project Management
Subject Matter Expert
People Management
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Employee Insights
Nick on a day in the life of a CRA
Nick Burger | Senior Clinical Research Associate
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Liliana on CRA tasks and our recognition program
Liliana Belmares Flores | CRA Line Manager
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Marlayna on why Parexel is a great place for CRAs
Marlayna Fitts | CRA Line Manager
Watch Video
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TEAM IMPRESSIONS
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Why Clinical Research Associates work at Parexel
Patient-focused in everything we do
We push the boundaries of what is possible to create clinical trials that are inclusive, innovative, and patient-focused
Supportive and inclusive environment
We foster collaboration, teamwork, respect, and inclusivity, to work together to achieve common goals.
Career growth and development
We develop your skills through training, mentorship, and career advancement programs.
Flexible work arrangements
We focus on outputs and results, not where and when you work.
Diverse therapeutic areas and project exposure
We continuously learn from a broad exposure from early to late phase clinical trials and our cros-functional global teams.
Advanced Technology
We recognize the importance of first-time quality to bring treatments to patients faster.
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Learn About Our Culture
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Benefits & Support
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