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Job Description
Clinical Project Manager Biotrial, Inc. - 2.7 Newark, NJ Job Details Full-time $90,000 - $120,000 a year 1 day ago Benefits Health insurance Dental insurance Paid time off Vision insurance 401(k) matching Life insurance Referral program Qualifications Teamwork Clinical research Bachelor of Science Writing skills Contract research organization experience Bachelor's degree Attention to detail Organizational skills Clinical trials Managing projects Productivity software Pharmaceutical research Project stakeholder communication Cross-functional communication Full Job Description Company Overview Biotrial , a leading provider of high-quality pharmacology services, is currently recruiting a Clinical Project Manager for Newark, NJ, US. With over 35 years of experience in providing scientific and medical services in Clinical Development, Biotrial possesses one of the largest clinical capacities in Europe and the U.S. The Clinical Project Manager is responsible for providing customer-focused leadership and project oversight. This position facilitates communication among team members, including sponsor personnel and the Biotrial Project Team. The Clinical Project Manager proactively solves issues and oversees the successful implementation and monitoring of clinical trials to ensure that those are conducted in accordance with ICH/GCP and applicable regulations. This position is based and will work in the Newark, New Jersey Clinical Pharmacology facility.
Responsibilities:
Under the supervision of the Associate Director, Clinical Operations, duties and responsibilities relative to the management of Clinical trials will include, but will not be limited to: Manage and coordinate the activities of clinical trials with the Biotrial Project Team (CRA, clinical team, Data Managers, Statisticians, Medical Writers, etc.). Serve as the main point of contact and communicate with sponsors regarding project timelines, updates, needs and emerging issues. Develop study timelines based on protocols. Ensure project start-up activities by facilitating processes for preparation of regulatory documents, ensuring timely IRB/IEC approvals for clinical trials. Lead the internal project meetings including Kick-off meetings and Study Initiation meetings, etc. with sponsors/internal teams. Follow screening and recruitment activities to ensure timely enrollment in the trials. Organize and coordinate Safety Review Meetings with Investigator / sub-investigator / Medical and scientific affair members. Monitor and ensure that project scope and deliverables are fulfilled within timelines and budget. Support and coordinate with the Medical Writing team to ensure completion of the Clinical Study Report, as applicable. Review and manage study contracts/budgets. Collaborate with Billing and Accounts Department to ensure billing agrees with pre-established milestones. Review and approve Vendor/Site contracts, budgets and invoices. Regularly and in a timely fashion, interact with management, sponsors, and/or functional team members on matters concerning resource allocation, project milestones, regulatory issues, and other relevant issues. Organize sponsors' visit of the Clinical Pharmacology Unit (Site qualification visits, Initiation Meetings, Monitoring visits and Close-out visits). Occasional travel may be required for bid defense, initiation or kick-off meetings, or other study-related activities.
Requirements:
Requires a B.S. degree in life sciences or related field. Minimum 2 years in managing projects in a Contract Research Organization (CRO) or industry. Experience in monitoring clinical studies is a plus. Good understanding of the drug development process. Excellent written and verbal communication skills, as well as interpersonal skills. Ability to interact with all levels of management, sponsor and study site personnel. Detail-oriented and possess good troubleshooting skills with the ability to prioritize and execute tasks in a high-pressure environment. Possess good trouble-shooting skills with the ability to prioritize and execute tasks in a high-pressure environment. Proficient computer skills in Microsoft Office Suite. By joining our Company, you become part of a high-performing organization. Teamwork and cooperation allow us to offer state-of-the-art services. The successful candidate will enjoy working in a multicultural environment and interacting in a supportive manner with different functional areas and locations. Equal Opportunity Employer Biotrial is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, genetics, disability, age, veteran status, or any other characteristic protected by law.
Pay:
$90,000.00 - $120,000.00 per year
Benefits:
401(k) matching Dental insurance Health insurance Life insurance Paid time off Referral program Vision insurance Application Question(s): Are you able to work onsite at the Clinical Pharmacology facility in
Newark, NJ Education:
Bachelor's (Required)
Experience:
contract research: 2 years (Preferred) monitoring clinical studies: 2 years (Preferred)
