Clinical Trial Oversight Manager (CTOM)

at  Amgen

Milano, Lombardia, Italy -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate22 Jan, 2025Not Specified23 Oct, 2024N/AClinical Research,Interpersonal Skills,Problem Solving,Clinical Research Experience,Clinical Trials,Cta,Communication Skills,Customer Service,Leadership,Critical Thinking,Life Sciences,Relationship Building,Independence,Leadership SkillsNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

HOW MIGHT YOU DEFY IMAGINATION?

Do more with the knowledge you’re working hard to acquire and the passion you already have. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Through this program, you will acquire the valuable hands-on skills and foundational experience to become the professional you are meant to be in your chosen field.

BASIC QUALIFICATIONS:

  • Doctorate degree OR
  • Master’s degree OR
  • BA/BS/BSc or qualified nurse (RN)
  • Work experience in life sciences or medically related field, including Biopharmaceutical clinical research experience (clinical research obtained working on clinical trials in a biotech, pharmaceutical or CRO company, or other relevant clinical setting)

PREFERRED QUALIFICATIONS:

  • Broad work experience working in life sciences or medically related field, including clinical site management experience, obtained working on clinical trials in a biotech, pharmaceutical or CRO company
  • Experience as a CRA, CTA, and/or Clinical/Regional Manager in the biopharmaceutical industry
  • Experience in a project leadership role
  • Experience working with or for Functional Service Provider or Contract Research Organizations
  • Supervisory Experience
  • Knowledge of or work experience with a biopharmaceutical GRDCA or QC department

KNOWLEDGE AND COMPETENCIES

  • Clinical Research: Familiarity with advanced concepts of clinical research, extensive knowledge of ICH/GCP regulations and guidelines, strong knowledge of clinical trial operations, and understanding of Functional Service Provider operational model.
  • Technical Skills: Computer and system operation skills.
  • Therapeutic Area: Relevant therapeutic area education and training.
  • Customer Service: Detailed understanding of customer service and demonstrated ability to anticipate and resolve problems.

Independence & Teamwork: Demonstrated ability to work independently with minimal supervision and effectively in a team/matrix environment on multiple projects.

  • Leadership & Influence: Excellence in relationship building, ability to lead and influence in a positive manner, and strong leadership skills.
  • Interpersonal & Communication Skills: Strong interpersonal skills, excellent organizational and planning skills, excellent oral and written communication, and business English fluency.
  • Quality & Detail: Attention to quality and detail, ability to identify and resolve problems, and attention to quality planning and execution.
  • Problem Solving & Flexibility: Ability for critical thinking, thinking out of the box, and flexibility.
  • Scientific Communication: Ability to write and present clearly using scientific and clinical issues terminology.

Responsibilities:

Please refer the Job description for details


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

Milano, Lombardia, Italy