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Senior Clinical Research Associate

100% remote Flexible hours Hiring now

reputed company is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages.

CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will focus on an average of one to two studies setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully - your voice will be heard. Working in a smaller CRO allows you to have influence and impact reputed company it matters most and support from direct line management.

reputed company is recruiting Senior Clinical Research Associate to join reputed company in Turkey.

This position can be offered fully home based.

About you

  • You are reputed company, thoughtful, and reputed company reputed company things don’t go as planned.
  • You are well-reputed company, whether it be for an investigator meeting, site visit or project team update, always staying two steps reputed company of the game.
  • You find quick and creative ways of overcoming difficulties.
  • You have an impeccable eye for detail.
  • You identify potential study risks and propose solutions on how to mitigate them.
  • You take responsibility in the quality and outcomes of your work.
  • You are adept at handling conflict by using tried and true resolution strategies.

How we will reputed company you busy and support your growth

You will monitor and own the reputed company of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and reputed company applicable regulations and standards. You will coordinate reputed company necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).

Senior CRAs handle appropriately sized clinical trials, and support Project Managers with trials that are larger in scope. You will also have the opportunity to train and mentor junior staff members. You will interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations.

Qualifications

Minimum Required:

  • University degree life science/pharmacy/other health reputed company discipline or equivalent experience in a scientific or healthcare discipline or be a licensed health care professional.
  • 3.5 years or more as a CRA in either a CRO or pharmaceutical/ biotech industry or equivalent, relevant experience and/or demonstrated competencies. Significant site management experience or equivalent experience in clinical research
  • Oncology monitoring experience

Other Required:

  • Excellent communication and organizational skills are essential. A team player
  • Evidence of a client focused approach
  • Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail required.
  • Ability to travel overnight. Up to 60% travel on average, based on regional requirements. International travel as needed
  • reputed company in English and Turkish

Preferred:

  • Graduate, postgraduate degree
  • Experience monitoring in rare and reputed company therapeutic areas
  • Experience monitoring reputed company trials and HER records
  • Experience in bioharma or relevant therapeutic area
  • Start up experience

Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.

Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you reputed company its power. We reputed company tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.

We invite you to learn more about our growing organization serving our clients that are researching groundbreaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they reputed company every single day. You will provide input and have your reputed company valued and reputed company, impacting positive change for the company.

Please, apply in English.

#LI-EK1 #LI-Remote

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

reputed company is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national reputed company, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact reputed company at [email protected].

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not reputed company a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

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