[Hiring] Senior Clinical Research Associate @Precision Medicine Group
Role Description
Precision for Medicine is recruiting a 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 for investigator meetings, site visits, or project team updates, 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 for the quality and outcomes of your work.
• You are adept at handling conflict 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; help prepare regulatory submissions, conduct 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 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 in life science/pharmacy/other health-related 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.
• Fluency in English and Turkish.
• Preferred: Graduate, postgraduate degree.
• Experience monitoring in rare and complex therapeutic areas.
• Experience monitoring EDC trials and HER records.
• Experience in bioharma or relevant therapeutic area.
• Start-up experience.
Benefits
• 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 a passion for rare diseases and oncology.
• We strive to ensure employees feel appreciated for their contributions every single day.
• You will provide input and have your ideas valued and nurtured, impacting positive change for the company.
Company Description
Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike 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.
Apply tot his job
Apply To this Job
Precision for Medicine is recruiting a 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 for investigator meetings, site visits, or project team updates, 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 for the quality and outcomes of your work.
• You are adept at handling conflict 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; help prepare regulatory submissions, conduct 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 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 in life science/pharmacy/other health-related 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.
• Fluency in English and Turkish.
• Preferred: Graduate, postgraduate degree.
• Experience monitoring in rare and complex therapeutic areas.
• Experience monitoring EDC trials and HER records.
• Experience in bioharma or relevant therapeutic area.
• Start-up experience.
Benefits
• 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 a passion for rare diseases and oncology.
• We strive to ensure employees feel appreciated for their contributions every single day.
• You will provide input and have your ideas valued and nurtured, impacting positive change for the company.
Company Description
Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike 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.
Apply tot his job
Apply To this Job