Home-Based Clinical Research Associate III (Oncology/Transplant)
The EMMES Corporation, established in 1977, is a woman-owned, private Contract Research Organization (CRO). Headquartered in Rockville, Maryland, Emmes employs over six hundred staff worldwide with offices located in Frederick, Maryland, Tysons Corner, Virginia, Vancouver, Canada and Bangalore, India. Ranked as a top area workplace of choice by the Washington Post, Emmes fosters an environment of collaboration, professional growth, and exceptional work life balance.
Our studies impact public health initiatives on a global scale occurring in more than sixty countries spanning across six continents. We are dedicated to providing statistical and epidemiological expertise, computer systems deployment, data management, study monitoring, regulatory guidance, and overall operational support to clients engaged in biomedical research. We offer comprehensive clinical research expertise from trial conception to marketing submission. Emmes is seeking four Clinical Research Associates III, preferably with experience in oncology, hematology, leukemia, bone marrow transplant and/or hematopoietic stem cell transplatation.
The Clinical Research Associate in collaboration with project teams is responsible for planning, monitoring, and coordinating clinical research studies at external study sites. As part of these activities, the Clinical Research Associate may also perform remote assessment of site activities, in addition to, onsite Investigator/site training, site qualification, initiation, interim, for cause, pharmacy and close out site monitoring visits. The Clinical Research Associate works closely with project team members to plan and support coordination of research at participating clinical sites. This goal is achieved by evaluating compliance with regulatory requirements, ICH guidelines, Standard Operating Procedures (SOPs), the study protocol and research objectives of the clinical trial. 75% travel each month is required. Travel may include international travel dependent upon project assignment.
Possesses detailed and current knowledge of the study protocol, site monitoring plan, study manuals, Good Clinical Practices and Code of Federal Regulations and local country regulatory requirements
Schedules and conducts site visits, including site qualification, initiation, interim, for cause, pharmacy and close out monitoring visits. Prepares and obtains required project approvals and ensures distribution of site visit reports within timelines, and tracks outstanding action items or tasks
Collects, reviews, maintains and/or provides required regulatory documents to designated sponsor or project representative. Review includes assessment of completeness, accuracy and compliance with regulatory and local agency requirements
Communicates and coordinates effectively with internal project staff members, site staff, sponsors, clients and other external colleagues
Coordinates with project team and other study personnel to determine data collection requirements based on the protocol, and may test electronic (or paper) case report forms, or the Monitoring Status Report (MSR) as required
Reviews, coordinates, contributes to and processes project documents and required reports, such as study protocol documents and consent forms, SAE, project and protocol deviation reports, accrual and other study status and/or study website reports
Reviews and contributes to the development and/or modification of study and project materials, such as Manual of Operating Procedures (MOPs), Monitoring Plans, User Guides and Data Management Handbooks
Works with sites during site monitoring visits to resolve protocol monitoring module discrepancies, as well as data discrepancies resulting from queries and Missing Forms & Values Reports
Attends and participates in sponsor, project and functional group meetings
Schedules and completes training in accordance with project needs and Emmes travel policies
Bachelor’s degree in a scientific discipline or equivalent experience; combination of training and experience will be taken under consideration
Ability to travel domestically and internationally up to 75%
Minimum of 4-6 years of clinical research/monitoring experience
Prior experience in solid tumor oncology, hematology and transplant studies preferred
Demonstrated understanding of regulatory obligations for a Clinical Research Associate and relevant ICH guidelines
Successful completion of ACRP CCRA or equivalent certification within one year of hire/transfer date
Skilled in prioritization, problem-solving, organization, critical thinking, decision-making, time management and planning activities
Self-motivated and high attention detail required
Ability to collaborate with internal and external colleagues and work well in team-oriented setting
Excellent oral and written communication; exceptional interpersonal skills
Ability to work remotely with a high degree of independence
Skilled in data management/computer proficient in Microsoft Office
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The EMMES Corporation is an equal opportunity affirmative action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.Back Email Apply Now