Contract CRA, Medical Device - IQVIA MedTech
Location: Morrisville, North Carolina
At IQVIA Biotech, we offer a unique approach to serving biotech customers. A flexible model, therapeutically-aligned teams and dedicated resources in a transparent partnership. As a Senior Clinical Research Associate, you’ll have the opportunity to work directly with customers in a collaborative environment where you'll be part of a team bringing important treatments to patients.
In this highly specialized and dynamic role, you’ll utilize your extensive therapeutic knowledge to oversee uniquely-focused clinical studies. Working at the core of clinical research, you’ll be exposed to cutting-edge protocols and experience a dedicated partnership with your team like never before.
Join us and help reimagine the future of biotech.
- Full Time
- Level: Senior
- Travel: Yes
What makes a Senior Clinical Research Associate at IQVIA Biotech successful? Check out the top traits we’re looking for and see if you have the right mix.
As you grow your CRA career at IQVIA Biotech, you’ll play an important role in helping our customers drive healthcare forward and impact the lives of patients around the world.
What makes IQVIA Biotech different from my past companies is that I partner directly with smaller pharmaceutical companies and am able to become a true ‘expert’ by being aligned with a smaller amount of projects with a larger site load. IQVIA Biotech promotes a strong culture of communication and mentorship and I’ve thoroughly enjoyed my time since joining last year.Leah, Clinical Research Associate 2
Resources that promote your career growth
Leaders that support flexible work schedules
Roles that require specialty knowledge and training
Protocols aligned to your specific expertise
Dynamic work environments that expose you to new experiences
Programs to help you build your therapeutic-knowledge
Contract CRA, Medical Device - IQVIA MedTech
IQVIA MedTech is seeking a Contract Sr. Clinical Research Associate for a full-time or part-time opportunity. CRA's must have experience with Medical Device. Prefer Women's Health experience.
ESSENTIAL JOB FUNCTIONS:
Participates in the preparation and execution of Phase I-IV clinical trials. Oversees the progress of clinical investigations by conducting site evaluation, initiation, and interim close out visits to sites. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors.
KNOWLEDGE, SKILLS AND ABILITIES:
Strong knowledge of clinical research process, including working knowledge of all functional areas of clinical trials and medical terminology.
5+ years of oncology monitoring experience, phase 1 AML experience required
Experience in monitoring and/or coordinating clinical trials required.
Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions.
Demonstrated ability to form strong functional relationships.
Excellent, presentation, organizational and interpersonal skills.
Ability to interact with all levels of staff to coordinate/execute study activities.
Ability to handle several priorities within multiple, complex trials.
Ability to reason independently and recommend specific solutions in clinical settings.
Ability to work independently, prioritize, and work within a matrix team environment.
Ability to mentor other CRAs and co-monitor, as required.
Knowledge of electronic data capture including basic data processing functions.
Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research.
MINIMUM RECRUITMENT STANDARDS:
BS/BA/BSc (or equivalent) in one of the life sciences or health care background (RPh, RN, etc) and a minimum of four (4) years of monitoring/site management experience is required; or equivalent combination of education, training and experience.
Prior Clinical Research Organization (CRO) experience preferred.
Experience working on inpatient or post op- surgical studies; Gastrointestinal would be a plus.
Prior project team leadership experience preferred.
Working knowledge of budget management preferred.
Must be able to travel domestically and internationally approximately 65%-85%.
Valid driver’s license
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer
Very limited physical effort required to perform normal job duties
Extensive use of telephone and face-to-face communication requiring accurate perception of speech
Extensive use of keyboard requiring repetitive motion of fingers
Regular sitting for extended periods of time
At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.
IQVIA, Inc. provides reasonable accommodations for applicants with disabilities. Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA’s Talent Acquisition team at firstname.lastname@example.org to arrange for such an accommodation.
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