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Clinical Research Jobs in New Jersey

Clinical Research Associate

Integrated Resources, Inc

South Plainfield, New Jersey

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JOB DETAILS
JOB TYPE
Full-time
SKILLS
Biotech and Pharmaceutical, Budget Management, Cardiovascular, Case Report Form (CRF), Clinical Data, Clinical Practices/Protocols, Clinical Research, Clinical Trial, Clinical Trial Management, Communication Skills, Contract Management, Contract Research Organization (CRO), Cross-Functional, Data Analysis, Data Cleaning, Drug Development, Electronic Data Capture (EDC), FDA Requirements, File Maintenance, GCP (Good Clinical Practices), Healthcare, Hematology, ICH Regulations, Information Technology & Information Systems, Informed Consent, Laboratory, Maintain Compliance, Medical Terminology, Medical Treatment, Microsoft Office, Nursing, Oncology, Operational Support, Organizational Skills, Pharmacy, Project Tracking, Quality Assurance, Reconciliation, Regulations, Regulatory Compliance, Regulatory Requirements, Regulatory Submissions, Rehabilitation Nursing, Research Nursing, Respiratory Medicine, Small Company, Staff Training, Standard Operating Procedures (SOP), Standards Development, Time Management, Vendor/Supplier Relations, Willing to Travel
LOCATION
South Plainfield, New Jersey
POSTED
Today
Clinical Research AssociateIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionThe Clinical Research Associate for Clinical Operation will provide site monitoring and management oversight across multiple clinical research trials in support of development of Pharmaceutical's drug pipeline. This position will report to Associate Director of Clinical Operations and be responsible for operational support for clinical studies and related activities in accordance with company standard operating procedures, good clinical practice, and applicable regulatory requirements.JOB RESPONSIBILITIES:Support project management oversight of Clinical Development activities for multiple domestic and international trials, including:Track study timelines;Review and track study budgets;Provide periodic updates on Clinical DevelopmentGradually develop responsibilities for management of contract research organization (CROs) activities for clinical and data managementProvide monitoring support, in some cases functioning as the primary site monitor.Assist in writing and review of protocols, amendments, and informed consent forms. Manage development of study-specific guidelines (Case Report Forms, Monitoring Plans, and Pharmacy Manuals, etc.)Collaborate with Quality Assurance Department in development of Clinical Development standard operating procedures (SOP).Perform investigative site trainingReview CRO, vendor, and internal SOPs to ensure consistency and proper delegation of responsibilities among study teams.Assist in development of vendor relationships with CROs, drug depots, country-specific laboratories, and other vendors, as needed.Provide internal support for site recruitment activities.Oversee Trial Master File maintenance and reconciliation.Provide support to Regulatory Department in regulatory activities including submissions, and review of regulatory documents.Ensure compliance with FDA regulations and ICH Good Clinical Practice guidelines, as well as country-specific guidelines.Ensure compliance with study-specific procedures.KEY CONSIDERATIONS:Collaborate in a cross-functional environment in a small biotechnology company to assist in the initiation and coordination of global clinical initiatives and strategies.A strong background as a clinical research associate (CRA), specifically site monitoring or, alternatively; a nursing background would be noteworthy, particularly if the candidate has worked as a nurse at a research site.A therapeutic background to complement our pipeline, i.e. Cardiovascular, Hematology, Oncology, Pulmonology.Well-versed in Good Clinical Practices, medical terminology, and standard study procedures.Experience with electronic data capture systems.Good quality background and experience with healthcare or pharmaceutical development is required.Must be driven to deliver quality results on time and in a highly ethical and professional manner;Candidate must be willing to travel internationally (up to 25-50%, potential more depending on enrollment).Great organizational and communication skills.Proficient in use of Microsoft Office applications.QualificationsThorough knowledge of Good Clinical Practice, clinical trial design, regulatory processes, and global clinical development process.3-5 years of investigative site monitoring or study coordinator/study nurse experience.Hands-on experience in data cleaning and analysis required.Proven ability to work independently, to lead a multidisciplinary trial team.Proven experience in developing effective relationships with key investigators.Ability to maintain effective working relationships with coworkers, managers, as well as investigative site personnel.EDUCATION: Undergraduate Degree

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