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| Citizen | GC |
| US Citizen | Student Visa |
| H1B | CPT |
| OPT | H4 Spouse of H1B |
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Employment Type:
| Full Time | Part Time |
| Permanent | Independent - 1099 |
| Contract – W2 | C2H Independent |
| C2H W2 | Contract – Corp 2 Corp |
| Contract to Hire – Corp 2 Corp |
Description:
IT’S MORE THAN A CAREER, IT’S A MISSION.
Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.
MINIMUM QUALIFICATIONS:
- At least 1 year of experience within clinical research, preferably within trial management
- Knowledge of pharmaceutical industry, regulatory process, clinical trials and medical terminology
Responsibilities:
Duties include but are not limited to:
- Manage SCRI’s Clinical Trial lead management inbox
- Send initial response to pharma/biotech/CRO contacts and collect required documents so study can be reviewed for scientific interest
- Create and maintain Lead Management tracking system to track metrics related to lead management process and research sites within appropriate systems (i.e. Florence eBinder) including uploading study documents and creating folders in clinical trial management systems (CTMS)
- Process, facilitate and track nondisclosure agreements
- Create and update both legacy CTMS systems and Florence as required
- Support feasibility process and site provisioning
- Follow detailed Lead Management process and escalate issues to supervisor to efficiently resolve any lead management related issues
- Other special projects as neede
Knowledge: A body of information needed to perform tasks; May be obtained through education, training or experience.
- Knowledge of pharmaceutical industry, regulatory process, clinical trials and medical terminology
- Entry-level professional position and on-the-job training. Typically, college graduate or equivalent experience. May be working towards relevant professional qualification
Abilities: An underlying, enduring trait useful for performing duties.
- Work closely managed and reviewed regularly. Follows specific, outlined, and detailed procedures.
- Problem solving skills in fast-paced environment
- Interpersonal skills and detailed-oriente
