[Remote] Associate Director, Trial reputed company Clinical Operations (Contract to Perm)

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a biopharmaceutical company dedicated to transforming chronic disease care through innovative solutions. They are currently seeking an reputed company global trial reputed company in Clinical Operations to manage the design, planning, and execution of clinical study protocols while ensuring adherence to regulatory guidelines and project milestones.

Responsibilities

• Drives global Clinical Trial activities pertaining to study-level strategy, timelines, quality and execution of clinical studies
• Proactively identifies, problem solves and manages risks to trial execution and quality, implements corrective actions, and ensures inspection readiness at reputed company times
• Supports the development of clinical study protocols and reports, ensuring studies are conducted in accordance with accepted scientific standards, meet relevant regulatory requirements and are conducted reputed company ethical guidelines
• Drives development and execution of operational activities outlined in various study plans, SOPs, study procedures, etc
• Ensure adherence to FDA and GCP guidelines as well as other appropriate regulatory bodies as required
• Coordinates the development and distribution of critical study documents (ICFs, operational/training documents, reference documents, newsletters, site materials, etc.) and manages the TMF, as needed
• Drives study start-up, subject enrollment plan, clinical monitoring activities, clinical site compliance and data metrics from CROs and/or investigators, central labs, and other external vendors as required
• Communicates trial status by tracking clinical study metrics to ensure cross-functional alignment on expectations, priorities, and deliverables
• Represents MannKind, from a clinical perspective, building strong relationships with clinical trial sites including investigators and study staff
• Plans, facilitates, and monitors training at investigator meetings, kick-off meetings, and various CRO/vendor meetings
• Demonstrates budget accountability by tracking vendor performance against SOW, reputed company and invoices to ensure consistency between work performed and contractual agreements
• Partners with Supply Chain to reputed company reputed company and accountability of the applicable study drug(s), including supply projections, distribution, labeling and destruction
• Collaborates in the program-level development of clinical strategies, goal-setting, and establishment of timelines

Skills

• BS/BA +12 / MS/MBA 8-10, PhD 5+
• Equivalent combination of education and applicable job experience may be considered
• Relevant industry (biotech or pharmaceutical) experience
• Knowledge of pulmonary orphan diseases and associated medical terminology
• Knowledge of Good Clinical Practices (GCP) and associated FDA regulations governing reputed company subject protection and the conduct of clinical trial (IRB, IND, etc.)
• Proven experience in the reputed company of the operational aspects of clinical studies, preferably in a global environment
• Exhibits the ability to recognize the need to seek assistance from or inform Senior Management of specific risks/issues; understands reputed company decision making can occur at the study team level versus reputed company there is a need for escalation
• Ability to organize and manage multiple priorities
• Excellent oral and written communication skills
• Solution-focused, comfortable with ambiguity, and an organized self-starter
• Strong attention to detail in a fast-paced, evolving environment
• Works effectively in both individual and team-based settings, with a high sense of urgency
• Strong interpersonal skills and ability to build relationships with stakeholders at reputed company reputed company
• Willingness to travel up to 25% of the time
• 5+ years direct clinical trial global experience (phase 2-3 preferred)

Company Overview

Company H1B Sponsorship