Odell Medical Search

No weekends/no call/no holidays required.. In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies for feasibility and evaluates potential competition with other protocols prior to submitting study.. Reviews study with principal investigator and/or clinical research coordinator to a budget outlining standard of care and research costs.. Recruits and evaluates potential study patients and works with clinical research coordinator to schedule required appointments and interviews.. Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC) is preferred.

clinical research

The Company: <ul><li> Named one of Americas 250 Best Hospitals </li><li> Patient Safety Excellence Award </li></ul> This company appreciates its employees: <ul><li> Medical, Dental and Vision </li><li> Flexible Spending Account </li><li> Health Savings Account </li><li> PTO </li><li> 401k Savings Plans </li><li> Many other discounts and programs </li></ul> The role you will play: <ul><li> 40hrs Day Shift, 4-10s. </li><li> No weekends/no call/no holidays required. </li><li> Assures that all protocol revisions, informed consents, continuing reviews, serious adverse events are submitted to the appropriate IRB of record in a timely manner. </li><li> Interacts with regulatory specialists and principal investigators and sub-investigators on all regulatory issues and changes within the protocol. </li><li> In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies for feasibility and evaluates potential competition with other protocols prior to submitting study. </li><li> Reviews study with principal investigator and/or clinical research coordinator to a budget outlining standard of care and research costs. Finalizes budget draft with budget coordinator. </li><li> Recruits and evaluates potential study patients and works with clinical research coordinator to schedule required appointments and interviews. </li><li> Identifies the needs of the patient population served and modifies and delivers care that is specific to those needs (i.e., age, culture, hearing and/or visually impaired, etc.) </li><li> This process includes communicating with the patient, parent, and/or primary caregiver(s) at their level (developmental/age, educational, literacy, etc.) </li></ul> Background Profile: <ul><li> Current and valid New Jersey Nursing license is required. </li><li> Must have Oncology Clinical Research experience. </li><li> Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC) is preferred. </li><li> Education on human subject research and GCP (CITI Training and Certification) is preferred. </li><li> Knowledge of clinical trials and the regulation (local, state, and federal) of such is preferred. </li><li> Familiarity with basic scientific and healthcare principles and terminology preferred. </li><li> BSN required. </li><li> Strongly prefer experience with medical oncology, solid tumors - GU, GI, Breast, Lung. </li></ul> <img src="https://www.jobg8.com/Tracking.aspx?SJ%2fd4OR7CJ850f%2bOtwv%2bhAk" width="0" height="0" />

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