• US Citizen

• Green Card

• EAD (OPT/CPT/GC/H4)

• H1B Work Permit

• Corp-Corp

• W2-Permanent

• W2-Contract

• Contract to Hire

• Consulting/Contract

• UG :- - Not Required

• PG :- - Not Required

• No of position :- ( 1 )

• Post :- 18th Jun 2025

- Working knowledge and understanding of FDA and ICH regulations and industry standards and quality control principles.
- Experience with all phases of drug development.
- Solid Experience in handling Clinical data acquisition and management from external/3rd Party vendors.
- May lead study level negotiation and agreement for data transfer or integration on behalf of company.
- Should be able to function collaboratively (with some guidance) with all levels of employees , moderate supervision required.
- Knowledge on FTP tools like GlobalScape, Clinical platforms like Veeva CDMS, Elluminate and Veeva TMF will be a plus.