Freelance Senior CRA
ICON, Atlanta, GA, United States
Freelance Senior CRA
ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
At ICON, our people set us apart. We value accountability, collaboration, partnership, and integrity, and aim to be the partner of choice in drug development.
Responsibilities
Work independently to coordinate activities for study setup and monitoring, completing accurate study status reports and maintaining study documentation.
Submit protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested.
Participate in preparing and reviewing study documentation and feasibility studies for new proposals.
Balance sponsor‑generated queries efficiently and ensure study cost‑effectiveness.
Depending on experience, assist in training and mentoring less experienced CRAs and/or lead CRAs on international projects.
Qualifications
18 months or more of monitoring experience in phase I‑III trials as a CRA.
Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data.
Excellent written and verbal communication in English.
Ability to produce accurate work to tight deadlines within a pressurized environment.
Travel at least 60% of the time (international and domestic, flying and driving) and possess a valid driving licence.
Benefits
Competitive salary packages and annual bonuses reflecting delivery of performance goals.
Health‑related benefits and retirement plans, including life assurance.
Global Employee Assistance Programme with 24‑hour access to a network of wellness professionals.
Optional benefits such as childcare vouchers, bike purchase schemes, gym memberships, subsidised travel passes, and health assessments.
ICON is an equal‑opportunity and inclusive employer committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process or in order to perform the essential functions of the position, please let us know.
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ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
At ICON, our people set us apart. We value accountability, collaboration, partnership, and integrity, and aim to be the partner of choice in drug development.
Responsibilities
Work independently to coordinate activities for study setup and monitoring, completing accurate study status reports and maintaining study documentation.
Submit protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested.
Participate in preparing and reviewing study documentation and feasibility studies for new proposals.
Balance sponsor‑generated queries efficiently and ensure study cost‑effectiveness.
Depending on experience, assist in training and mentoring less experienced CRAs and/or lead CRAs on international projects.
Qualifications
18 months or more of monitoring experience in phase I‑III trials as a CRA.
Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data.
Excellent written and verbal communication in English.
Ability to produce accurate work to tight deadlines within a pressurized environment.
Travel at least 60% of the time (international and domestic, flying and driving) and possess a valid driving licence.
Benefits
Competitive salary packages and annual bonuses reflecting delivery of performance goals.
Health‑related benefits and retirement plans, including life assurance.
Global Employee Assistance Programme with 24‑hour access to a network of wellness professionals.
Optional benefits such as childcare vouchers, bike purchase schemes, gym memberships, subsidised travel passes, and health assessments.
ICON is an equal‑opportunity and inclusive employer committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process or in order to perform the essential functions of the position, please let us know.
#J-18808-Ljbffr