Medical Science Liaison (Renal Transplant), FSP
at Thermo Fisher Scientific
Home Office, Iowa, Czech -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 10 Apr, 2025 | Not Specified | 13 Jan, 2025 | N/A | Medicine,Regulations,Regulatory Requirements,Kidney,Insight Generation,Intelligence | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
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:
JOB DESCRIPTION
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies.
SCIENTIFIC/MEDICAL EXCHANGE AND EDUCATION, AND INSIGHT GENERATION
- Ensure timely and informative scientific/medical exchanges with external stakeholders that accurately reflect scientific data.
- Deliver high quality scientific/medical education in a variety of settings, including related to diseases of interest, clinical studies (focus on our DGF trial and in 2nd line AMR Trial), investigational products and any future licensed products.
- Obtain feedback that can be disseminated throughout the organization.
- Coordinate the timely and appropriate response to internal and external Medical Information enquires, utilizing client medical information resources and in line with regulatory requirements.
- Attend appropriate local, national and international meetings and congresses to gather intelligence, develop productive collaborations, engage in scientific exchange and ensure insights are shared within the client
EDUCATION, EXPERIENCE
- Scientific, healthcare or medical degree (MS, PharmD, PhD, MD, RN, PA)
- Significant field-based experience in a biopharmaceutical industry in medical affairs
- Clinical experience in Medicine (Kidney or other solid organ) is an advantage
- Knowledge of regulations and practices related to industry interactions with healthcare professionals
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
Home Office, Czech