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CRAII/SCRA - FSP - Single sponsor (Turkey)

extra holidays - extra parental leave - fully flexible
Remote: 
Full Remote
Contract: 
Full time
Experience: 
Mid-level (2-5 years)
Work from: 
Turkey

Offer summary

Qualifications:

Minimum 2 years as a Clinical Research Associate, Bachelor’s degree in a related discipline, Experience in Pharma, CRO, or Biotech, Strong oncology experience.

Key responsabilities:

  • Prepare, initiate, monitor, and close studies
  • Collaborate with local study teams and sites

Parexel logo
Parexel XLarge http://www.parexel.com
10001 Employees
About Parexel
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.
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Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Parexel FSP is hiring Clinical Research Associates, from all levels to join us on a permanent full-time, home-based basis.

Dedicated to a single sponsor in BioPharma, who is revolutionizing healthcare by harnessing the power of science to benefit people, society, and the planet. Turkey is a vital part of their global network, hosting colleagues from every segment of the life sciences value chain. Their science-driven approach aims to transform healthcare and improve patient outcomes, while also fulfilling a purpose-led role in society.

Job Purpose:

As a Clinical Research Associate (CRA)/Clinical Monitor, you will have local responsibility for the delivery of the studies at allocated sites and will be an active participant in the local study team(s). You will work in close collaboration with other Monitors and the Local Study Team to ensure that quality and quantity commitments are achieved in a timely and efficient manner. You will be the main contact with the study site and will have responsibility for the proper conduct of the study.

The CRA is responsible for the preparation, initiation, monitoring, and closure of an agreed number of centers in clinical studies according to Procedural Documents, international guidelines such as ICH and GCP as well as relevant local regulations, and that the centers deliver according to the commitment in the individual trials.

A CRA with longer tenure and experience may take on additional responsibilities, including tasks associated with the Local Study Manager.

Requirements:

  • Minimum 2 years of experience as a Clinical Research Associate conducting all visits.

  • Experience gained ideally in Pharma, CRO, or Biotech.

  • Good understanding of Clinical Study Management including monitoring, study drug handling, and data management.

  • Bachelor’s degree in a related discipline, preferably in life science, or equivalent qualification.

  • Strong oncology experience.

Apply today!

#LI-TA1

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Hard Skills

Continuous MonitoringOncologyClinical ResearchData ManagementDrug AdministrationgRPCClinical Study DesignPharmacy Experience

Other Skills

  • Collaboration
  • Communication
  • Problem Solving
Are you interested?

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