1. Carries out research within the scope of the established study protocol. Adheres to all human subjects regulations as defined by Yale University and the federal government that pertain to research studies. 2. Develops criteria for admission of study subjects based on goals and objectives of project. 3. Determines potential sources of funding and prospective partnerships. 4. Evaluates feasibility of accepting potential projects through analysis of staffing needs, resource requirements, financial costs, and current planned capacity of group. Negotiates contracts and/or changes with funder. 5. Develops original HIC/IRB submissions.  Based on knowledge of science and research goals, collaborates with PIs on major revisions and contributes to scientific protocols.  Plans and implements changes. 6. Develops forms, questionnaires and the application of research techniques; writes procedures manuals for data collection and coding. 7. Responsible for the documentation and transmission of study data.  Ensures that report forms are accurately documented and completed in a timely manner at each site location. 8. Works independently to develop manage and organize multi site studies.  Serves as primary coordinator between University, non-Yale collaborators, pharmaceutical companies, HIC, IRB and funding sources. 9. Performs descriptive and multivariate statistical analyses of data, using computer software. 10. Designs and implements quality control measures to ensure accurate collection and processing of data. 11. Contributes in-depth, original thought and relevance to written reports and to the writing of abstracts and manuscripts.

Preferred Education:  Health science degree in Biological or Behavioral Sciences, Science-Medical Writing, Science Communication, or other related field. Strong and proven background in laboratory or clinical research and regulatory aspects.

Preferred Education, Experience and Skills:  Health science degree in Biological or Behavioral Sciences, Science-Medical Writing, Science Communication, or other related field. Strong and proven background in laboratory or clinical research and regulatory aspects.

Posting Position Title:  Research Associate 2, HSS

Required Skill/ability 3:  Skilled in developing formal presentation content (including abstracts, posters, slides, and manuscripts). Organize and participate in meetings and conference calls with key internal and/or external partners/stakeholders; capture and communicate action items; facilitate follow-up on action items.

Work Week:  Standard (M-F equal number of hours per day)

University Job Title:  Research Associate and Project Manager

Required Skill/ability 1:  Able to independently plan and execute optimal biospecimen collection, distribution and reporting for the institutional thoracic oncology repository.

Required Skill/ability 4:  Capacity to assume project manager role for those projects that entail primarily medical writing department deliverables.

Required Skill/ability 2:  Able to organize project activities and elaborate scientific documents including sections of grant applications, scientific manuscripts, clinical trial protocols, biomarker budgets, progress reports, HIC/IRB submission and other regulatory documents.

Masters Degree in a related discipline and two years of experience or an equivalent combination of education and experience.

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