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Job Description
- Req#: 744000099368195
Employer Industry: Contract Research Organization
Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Engaging work environment focused on stability and innovation
- Participate in impactful global clinical projects
- Involvement in cutting-edge therapies, including Oncology and Cell Therapy
- Supportive team atmosphere with opportunities for mentorship and training
What to Expect (Job Responsibilities):
- Coordinate investigator/site feasibility and identification processes, as well as study startup
- Monitor project timelines and patient enrollment, implementing corrective and preventive measures as needed
- Manage the query resolution process and ensure compliance in monitoring visit reports
- Conduct initial training and provide mentorship for newly promoted Lead Clinical Research Associates (CRAs)
- Oversee project teams in site contracting, payments, and compliance evaluations
What is Required (Qualifications):
- Relevant educational background, such as MD, MPharm, RN, or a degree in Life Sciences or equivalent
- Minimum of 4 years' site monitoring experience, including participation in global clinical projects as a Lead Monitor
- Experience with all types of monitoring visits in Phase II and/or III
- Proficiency in MS Office applications
- Ability to travel up to 50% based on project needs
How to Stand Out (Preferred Qualifications):
- Strong experience in Oncology
- Experience in CAR-T Therapy or other types of Cell Therapy, Gene Therapy, Radiation Therapy, or Nuclear Medicine
- Strong experience in gastrointestinal conditions (Chron's, Ulcerative Colitis, IBS)
- Excellent communication and collaboration skills
#ContractResearch #ClinicalTrials #Oncology #CareerGrowth #TeamCollaboration
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