We are seeking an Experienced Clinical Research Associate (CRA).
Position Overview:
Performs and coordinates different aspects of the clinical monitoring and site management process.
Conducts remote or on-site visits to assess protocol and regulatory compliance and handles required documentation. Manages procedures and guidelines from different sponsors and/or monitoring environments (i.e. FSO, FSP, Government, etc.).
Acts as a site processes specialist, ensuring that the trial is conducted according to the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability. Ensures audit readiness.
Develops collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to role are outlined in the task matrix.
Position Overview:
Performs and coordinates different aspects of the clinical monitoring and site management process.
Conducts remote or on-site visits to assess protocol and regulatory compliance and handles required documentation. Manages procedures and guidelines from different sponsors and/or monitoring environments (i.e. FSO, FSP, Government, etc.).
Acts as a site processes specialist, ensuring that the trial is conducted according to the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability. Ensures audit readiness.
Develops collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to role are outlined in the task matrix.
Requirements:
Bachelor's degree in a life sciences field.
Clinical monitoring experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1-2 years) in a clinical environment where experience is gained in clinical trials, medical terminology, medical research, clinical research or health care or experience in a health sciences field with formal training in medical terminology and anatomy may be considered.
Valid driver's license where applicable.
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills & Abilities:
Basic medical/therapeutic area knowledge and understanding of medical terminology.
Ability to attain and maintain a proven understanding of ICH GCPs and industry regulations and procedural documents.
Good oral and written communication skills, with ability to communicate effectively with medical personnel.
Good interpersonal skills.
Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers underlying issues.
Good organizational and time management skills.
Ability to remain flexible and adaptable in a wide range of scenarios.
Well-developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving.
Ability to manage Risk Based Monitoring concepts and processes.
Ability to work in a team or independently as required.
Good digital literacy: proven knowledge of Microsoft Office and ability to learn appropriate software.
Good English language and grammar skills.
Bachelor's degree in a life sciences field.
Clinical monitoring experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1-2 years) in a clinical environment where experience is gained in clinical trials, medical terminology, medical research, clinical research or health care or experience in a health sciences field with formal training in medical terminology and anatomy may be considered.
Valid driver's license where applicable.
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills & Abilities:
Basic medical/therapeutic area knowledge and understanding of medical terminology.
Ability to attain and maintain a proven understanding of ICH GCPs and industry regulations and procedural documents.
Good oral and written communication skills, with ability to communicate effectively with medical personnel.
Good interpersonal skills.
Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers underlying issues.
Good organizational and time management skills.
Ability to remain flexible and adaptable in a wide range of scenarios.
Well-developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving.
Ability to manage Risk Based Monitoring concepts and processes.
Ability to work in a team or independently as required.
Good digital literacy: proven knowledge of Microsoft Office and ability to learn appropriate software.
Good English language and grammar skills.
This position is open to all candidates.
