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Precision Medicine Group

Clinical Research Associate II/ Senior Clinical Research Associate

Work from homeNew this week

Remote role where the employee must remain based in a particular country.

Turkey only

Employer listed it 2 days ago · Found 10h ago

First listed 2 days ago.

Salary

Not stated

Location

Turkey only

Timezone

Not stated

Contract

Full-time

Experience

Senior

Category

Other

This employer didn't state pay. Jobs like this usually pay around $125k–$205k a year, a typical range taken from 166 senior-level other roles on Nomaders that do state pay. It's a guide, not an offer.

Remote flexibility

Work from home

This is a remote role, but the employee must be based in Turkey. It is work from home rather than work from anywhere.

What the employer says

  • Source listing states candidate location: "Remote, Turkey, Remote (Turkey)"

What Nomaders makes of it

  • Residency required in Turkey
  • Payroll and tax are likely handled in that country only

The quotes above are the employer's own words; the reading is ours. Always check the original listing and employment terms before working from another country.

About the role

Precision for Medicine 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 when it matters most and support from direct line management.

Precision for Medicine is recruiting Clinical Research Associate II/ Senior Clinical Research Associate to join our team in Turkey.

This position can be offered fully home based.

About you:

You are calm, thoughtful, and responsive when things don’t go as planned.

You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead 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 keep you busy and support your growth:

You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all 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.).

Qualifications:

Minimum Required:

University degree life science/pharmacy/other health related discipline or equivalent experience in a scientific or healthcare discipline or be a licensed health care professional.

At least 2 years of experience as a CRA in either a CRO or pharmaceutical/ biotech industry or equivalent, relevant experience and/or demonstrated competencies. Site management experience or equivalent experience in clinical research

Oncology monitoring experience.

CAR-T 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.

Requirements

  • ·You are calm, thoughtful, and responsive when things don’t go as planned.
  • ·You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead 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.

Benefits

No benefits package published with this listing. Ask about it at first interview.

How to apply

  1. 1Check the flexibility label above, work from home, matches where you plan to live and work.
  2. 2Tailor your CV to the role at Precision Medicine Group, mentioning your remote working experience.
  3. 3Apply directly on the employer's careers page using the button below. Nomaders never handles your application.

Found 11h ago. Last checked 23 Sept. Always confirm the details on the original posting, salary and location can change after publication.

Listing sourced from Company boards.

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