• 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 :- 12th Jul 2025

o    Minimum of 3-5 years of project management experience in the pharmaceutical, biotechnology, or clinical research industry.
o    Strong experience in managing clinical trials utilizing eCOA systems (e.g., ePRO, eConsent, and other electronic data capture solutions).
o    Proven expertise in managing Digital Clinical Trials (DCT), including the use of remote monitoring, telemedicine, wearable devices, and patient-centric solutions.
•    Technical Knowledge:
o    Strong understanding of eCOA platforms, clinical trial management systems (CTMS), and data management systems.
o    Familiarity with digital trial technologies (e.g., wearables, telemedicine tools, mobile apps) and remote patient monitoring platforms.
o    Knowledge of regulatory requirements for eCOA and DCT, such as 21 CFR Part 11, ICH E6, and HIPAA compliance.
•    Project Management Expertise:
o    Excellent project management skills, including scope definition, budgeting, timeline management, and risk assessment.
o    PMP (Project Management Professional) or other relevant certifications preferred.
o    Ability to manage multiple projects simultaneously while meeting deadlines and maintaining quality standards.
•    Communication & Leadership:
o    Strong communication, presentation, and interpersonal skills, with the ability to influence and engage stakeholders at all levels.
o    Proven leadership skills with the ability to manage cross-functional teams and external vendors effectively.
•    Problem Solving & Analytical Thinking:
o    Strong problem-solving abilities, with a proactive approach to identifying and resolving issues.
o    Ability to analyze complex data and provide actionable insights to stakeholders.