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Job Description
- Req#: 744000103146386
Employer Industry: Contract Research Organization
Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Engaging work environment focused on innovation and quality service
- Chance to work on global clinical projects in diverse therapeutic areas
- Competitive salary and benefits package
- Opportunity to mentor and train new team members
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 project team in site contracting and payments
- Conduct site audit preparation visits and coordinate resolution of audit findings
- Deliver trainings and presentations at Investigator Meetings
What is Required (Qualifications):
- Relevant educational background, such as MD, MPharm, RN, or a College/University degree in Life Sciences
- Minimum of 4 years' site monitoring experience with participation in global clinical projects as a Lead Monitor or equivalent
- Experience with all types of monitoring visits in Phase II and/or III
- Full working proficiency in English
- Excellent communication, collaboration, and problem-solving skills
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 Radiopharmaceuticals
- Strong experience in GI (Crohn's, Ulcerative Colitis, IBS)
- Ability to travel up to 50% depending on project needs
#ContractResearch #ClinicalTrials #CareerOpportunity #Oncology #LifeSciences
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