Connexion strives to be the unrivaled staffing solution for both job seekers and hiring organizations by expertly connecting talent with opportunity. We build world class teams for our customers, and better the lives of our candidates by providing them with fulfilling careers.
Connexion would like to provide you with details about this new opportunity as we are seeking individuals with the following skills:
Manager, Clinical Data Management
Duties: The Manager, Clinical Data Management leads the data management components of a clinical trial ranging from small early phase to large global and late phase programs. The Manager, Clinical Data Management is responsible for ensuring study launch, conduct, and closeout are performed according to our quality standards, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), and International Conference on Harmonization (ICH) guidelines to fulfill all federal and local regulations. The assigned clinical trial(s) may be high complexity or high risk. Duties include serving as the primary data management liaison with vendors and senior management. This position will manage essential duties and responsibilities as independently as possible, with guidance and oversight provided by senior data management when needed.
Skills: Maintain effective communication with vendors and our internal project team through oral and written correspondence, project status and progress reports. Manage the planning, implementation and overall direction of executing clinical trial data management activities including protocol review, electronic system configuration, Case Report Form (CRF/eCRF) design, database development, validation programming, and discrepancy management. Prepare information for internal meetings.
Maintain and evaluate project progress by managing timelines and other tracking/analysis tools. Design, produce and distribute standard and customized status, resourcing, and tracking reports as well as functional area plans, to appropriate team members and senior management. Work on problems of a diverse scope. Exercise judgment in managing tasks within generally defined practices and policies in selecting methods and techniques to track and manage timelines, risk, and data quality.
Manages the cross-functional collaboration, development, and maintenance of the components of the study Data Management Plan (DMP) and data management deliverables including the Case Report Form (CRF), CRF completion guidelines, SAS annotated CRFs, data handling plan, data review plan, edit check specifications, data transfer specifications, data quality plan, etc. Manage the interaction with data management vendors to ensure that data management tasks remain on target according to project timelines. Proactively organize on-going data review throughout the conduct of the study to ensure timely and appropriate identification of errors and discrepancies. Facilitate the correction of errors and discrepancies through the site query process, document permanent data issues, communicate issues with team members, and deliver a quality locked database for analysis. Provide input to the data management study budget and responsible for managing assigned vendor budget(s). Lead new data management initiatives such as establishing capacity for electronic data capture and clinical outcome assessments. Conduct CRO data management function inspections and audits. Contribute to the development and implementation of departmental policies, standards and process improvement initiatives.
Education: A bachelor's degree in clinical, biological or mathematical sciences, nursing degree, or equivalent related field education and experience is required. A master's degree is preferred. A minimum of 8 years actively managing clinical research projects in collaboration with other functional areas with at least 2 years successfully managing CROs is CROs is preferred. Previous supervisory, oncology and/or central nervous system experience is preferred. A thorough knowledge of FDA regulations, drug development and clinical monitoring procedures is required. Demonstrated problem solving abilities and strong presentation, documentation, organizational, and interpersonal skills as well as a team-oriented approach are required. Excellent written and verbal communication skills are required. Demonstrated proficiency with ICH, GCDMP, and GCP is required. Fluent English is required. Proficient computer skills using Word, Excel, PowerPoint, MS Project, email and the internet are required. Demonstrated self-starter with the ability to mentor and handle multiple tasks to meet deadlines while delivering high quality work in a dynamic work environment. Must possess excellent project management skills and have demonstrated ability to develop data management processes and training.
Skills and Experience:
CASE REPORT FORM
CLINICAL DATA MANAGEMENT
EXCELLENT WRITTEN AND VERBAL COMMUNICATION SKILLS FDA GCP ICH INSPECTIONS LIAISON MAINTENANCE MENTOR MS PROJECT ONCOLOGY POWERPOINT PROBLEM SOLVING PROCESS IMPROVEMENT PROJECT MANAGEMENT SAS SELF-STARTER SYSTEM CONFIGURATION TRAINING WORD AUDIT CLINICAL TRIAL CONDITIONAL RANDOM FIELD CORRESPONDENCE
Date Posted: 9/13/2019
Hiring Organization: Connexion Systems & Engineering
Job Title: Manager, Clinical Data Management
Location: San Francisco, CA
Employment Type: Full Time, Contract
Pay Range: 71/hr.
Duration: 12 months
Job #: bh10430
When responding to this job posting you MUST include the Job# and Job Title in your subject line.
If you are active in a job search but this job is not for you, please reach out to email@example.com. We would be glad to help you find the perfect job!
ConneXion Systems & Engineering
490 Boston Post Road
Sudbury, MA 01776