DOCS is currently seeking experienced monitors for a Sr. Clinical Research Associate opportunity based in Chicago, IL. This position is a home-based position for someone with 5+ years of on-site Early Development Oncology monitoring experience for a CRO or Pharmaceutical Company. Responsibilities: Expedites the pre-study and study initiation processes including the conduct of Pre-Study valuation and Site Initiation visits. Conducts Site Initiation visits in collaboration with Site Managers and/or Clinical Trial Managers, where applicable, to or...

DOCS is hiring!  We have an excellent opportunity available for the right candidate!  DOCS is an excellent company that values their employees.  We have excellent benefits as well.   Performs the role of Local Trial  Manager (LTM)  including operational  oversight of assigned protocol(s) from start-up through to database  lock and closeout activities as described  in GCO procedural documents. May perform the role of Global Trial Manager (GTM) for single country as described  in  GCO procedural documents.  LTM is a person within Trial Co-ordinati...

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Our client, a nationally acclaimed interdisciplinary research center in Mississippi is strategically adding a long-term, career-oriented Enterprise Java Architect -Developer. A niche player with a highly skilled team of researchers, data scientists and software professionals delivering the best-of-class data, software applications and tools specific to the social sciences space (healthcare, workforce, education, demographics, addiction, discrimination, etc.) used by local, state and federal agencies and gaining traction internationally. A newer, $4...

• Contributing to the preparation of Training Materials (Investigator Meetings, Site Evaluation and Initiation Training) • Managing process for planning and procuring ancillary clinical supplies • Facilitating and collating country recruitment plans • Creating and managing study specific tools such as recruitment and retention materials and study newsletters • Maintaining study level storyboard • Facilitating authoring of Investigational Product Information Manual (IPIM) and study specific Important Protocol Deviation (IPD) list • Compiling...

Responsible for managing data management teams, studies and programs of studies under the general direction of Sr. Project Manager or the Director of Data Management. • Work with Clinical Operations, CDMS, Biostatistics, CDS, ITG, Medical Writing, Regulatory Affairs and Quality Assurance to ensure that data collected during trials are managed according to corporate standards and meet regulatory guide lines for data integrity.

Summary: Responsible for the development and analysis of contractual relationships including investigator grants including but not limited to drafting, negotiating, and finalizing agreements related to clinical trials. Provide support to the clinical team in the pricing, planning, execution and control of grants and contracts. Principal Responsibilities: Responsible for analyzing contract requests/needs from operating companies and translating into appropriate contracts/budgets for company sponsored and investigator initiated clinical tr...

Job Title: Clinical Research Associate Experience: 3+ years Therapeutic areas:Oncology Location: Canada Roles & Responsibilities of the position PRINCIPAL RESPONSIBILITIES: - Participates in site feasibility and/or pre-trial site assessment visits, providing recommendation from local area about site/investigator selection in collaboration with the trial team - Acts as primary local company contact for assigned sites for specific trials. - Attends/participates in investigator meetings as needed. - Responsible for executing activities...