Start Date
Immediate
Expiry Date
05 Jun, 25
Salary
0.0
Posted On
05 Mar, 25
Experience
3 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
Document Management, Finance, Credentials, Clinical Research
Industry
Pharmaceuticals
JOB SUMMARY:
The Clinical Research Documents and Budgets Specialist is responsible to negotiate, execute, and maintain the integrity of basic to complex Industry and grant sponsored research agreements and contracts for clinical trials as well as other agreements relevant to the Clinical Research Institute (CRI); to develop, negotiate, and coordinate budgets for industry sponsored research clinical trials, each in accordance with St. Elizabeth Clinical Research Institutes policies, various human subject research certifications and federal laws and regulations; to identify, resolve or mitigate regulatory compliance, financial, intellectual property and other risks; to advise, support, guide and provide consultation to the Research Team on feasibility and financial management of industry sponsored research clinical trials to develop and support a sustainable clinical research program that leads to improvements in medical care for patients.
Demonstrate respect, dignity, kindness and empathy in each encounter with all patients, families, visitors and other employees regardless of cultural background.
EDUCATION, CREDENTIALS, LICENSES:
SPECIALIZED KNOWLEDGE:
KIND AND LENGTH OF EXPERIENCE:
FLSA STATUS:
Exempt
Right Career. Right Here. If you’re looking for the right careers in healthcare, the right place to be is at St. Elizabeth. Join us, and you’ll take pride in the level of care we offer our community
Please refer the Job description for details