Principal Operational Quality and Compliance Specialist
at Thermo Fisher Scientific
Indiana, Indiana, USA -
| Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
|---|---|---|---|---|---|---|---|
| Immediate | 09 Oct, 2024 | Not Specified | 10 Jul, 2024 | 8 year(s) or above | Clinical Research Experience,Decision Making,Communication Skills,Close Out,Management Skills,Regulatory Guidelines,Directives,English,Analytical Skills,Clinical Trials,Collaboration,Writing,Training,Digital Literacy | 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.
EDUCATION
- Bachelor’s degree or equivalent and relevant formal academic / vocational qualification
EXPERIENCE
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years).
- Significant clinical research experience in all phases of clinical study life cycle, including start-up, interim and close-out, is preferred.
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities:
- Strong judgment, decision making, issue resolution and risk management skills.
- Broad understanding of procedural documents
- Mature investigative and analytical skills
- Familiarity with the practices, processes, and requirements of clinical trials
- Broad understanding of clinical management technology and systems, and strong digital literacy
- Strong ability to influence
- Effective oral and written communication skills including the ability to communicate in English, both orally and in writing
- Capable of advising and promoting collaboration in a multi-disciplinary and/or multi-cultural team setting
- Broad understanding of regulatory guidelines and directives
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:8.0Max:13.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Indiana, USA
