What are the responsibilities and job description for the US Feasibility Manager position at VARITE INC?
VARITE is looking for qualified US Feasibility Manager in Ridgefield, CT.
WHAT THE CLIENT DOES?
A global, research-driven pharmaceutical company that focuses on developing innovative medicines in areas such as human pharmaceuticals, animal health, and biopharmaceutical contract manufacturing.
WHAT WE DO?
Established in the Year 2000, VARITE is an award-winning minority business enterprise providing global consulting & staffing services to Fortune 1000 companies and government agencies. With 850 global consultants, VARITE is committed to delivering excellence to its customers by leveraging its global experience and expertise in providing comprehensive scientific, engineering, technical, and non-technical staff augmentation and talent acquisition services.
Job Title: US Feasibility Manager
Location: Ridgefield, CT (Remote)
Contract Duration: 12 months (Possible Extension)
Pay Rate Range: $ 54.77/hr. to $ 58.68/hr. on W2
Work Authorization: Only USC or GC
It can be fully remote but needs to be able to work EST hours. Little to no travel involved.
HERE’S WHAT YOU’LL DO
Duties:
- Responsible for the development and deployment of comprehensive country and site feasibility assessments across Client trials and programs within the US.
- Ensures recommendations are tactically feasible and considerate of the indications/assets from a holistic industry perspective.
- In close alignment with internal stakeholders, identifies highly capable investigators/sites to meet study requirements and business needs. Applies expertise as a systems and database subject matter expert to provide quality feasibility outputs. s and databases.
Skills:
- Experience as a Clinical Research Coordinator, Clinical Monitor, Field Monitor, or Site Manager is highly desired.
- Demonstrated experience in the regulated pharmaceutical or healthcare industry required; a minimum of at least four (4) years experience is preferred.
- Candidates should have experience managing global and local/regional feasibilities.
- Must have basic knowledge and experience in clinical medicine with an ability to evaluate data and scientific literature; must understand and implement FDA/ICH GCP regulations; in addition to advanced understanding of sponsor criteria necessary to qualify sites and staff to perform clinical human trials Phases I-IV.
- Thorough understanding of all phases of drug development (I-IV).
- Understanding of federal regulations pertaining to IND and NDA regulations.
- Excellent analytical skills and critical thinking abilities required, including an ability to anticipate issues and pro-actively problem-solve.
- Familiar with the supported Medical applications and an understanding of technologies used by these applications.
- Proficient in Word, Excel, Adobe Acrobat Professional.
Education:
- Bachelor's Degree (Life Sciences preferred (BA, MS, PhD)) or Diploma in Nursing (RN) or degree in Pharmacy from an accredited institution.
BENEFITS:
We offer a comprehensive benefits package designed to support the health, well-being, and financial security of our employees and their families. Eligible employees may receive:
- Health Insurance: Medical, dental, and vision coverage
- Retirement Plans: Participation in a company-sponsored retirement savings plan.
- Legal Service Plans: Offering access to attorneys for legal advice and representation.
If this opportunity interests you, please respond by clicking on EasyApply.
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VARITE is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
Salary : $55 - $59