Associate Director

MannKind Corporation is a biopharmaceutical company dedicated to transforming chronic disease care through innovative, patient‑centric solutions. We develop and commercialize inhaled therapeutics and drug‑device technologies aimed at addressing serious unmet needs across endocrine, cardiorenal, and orphan lung diseases, applying deep expertise in formulation science and inhalation‑device engineering to reduce the treatment burden for conditions such as diabetes, congestive heart failure, pulmonary fibrosis, and pulmonary hypertension. MannKind’s core technologies, including ultrafine dry‑powder formulations and advanced inhalation platforms, enable rapid, convenient delivery of medicines directly to the deep lung, supporting both local pulmonary targeting and systemic delivery. Position Summary MannKind Corporation is currently seeking an experienced global trial lead, Clinical Operations to lead/support the design, planning, implementation and execution of clinical study protocols, operational plans and study timelines for MannKind trials. The role will manage all aspects of study progress, including protocol design, development and planning, study initiation, execution and close‑out, and support the development of clinical study reports, abstracts for professional meetings and publications. The role will ensure adherence to all appropriate regulatory guidelines as well as support the development and implementation of clinical processes, procedures and programs. The role will ensure that project/department milestones and goals are met, adhering to approved budgets. Key part of this role is to coordinate the study execution in collaboration with internal team, CROs and contractors. This is an exciting opportunity to help build our company narrative and collaborative partnerships with key opinion leaders and investigators. Temp to Hire Principal Responsibilities Drive global Clinical Trial activities pertaining to study-level strategy, timelines, quality and execution of clinical studies Proactively identify, problem‑solve and manage risks to trial execution and quality, implement corrective actions, and ensure inspection readiness at all times Support 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 within ethical guidelines Drive 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 Coordinate the development and distribution of critical study documents (ICFs, operational/training documents, reference documents, newsletters, site materials, etc.) and manage the TMF, as needed Drive 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 Communicate trial status by tracking clinical study metrics to ensure cross‑functional alignment on expectations, priorities, and deliverables Represent MannKind, from a clinical perspective, building strong relationships with clinical trial sites including investigators and study staff Plan, facilitate, and monitor training at investigator meetings, kick‑off meetings, and various CRO/vendor meetings Demonstrate budget accountability by tracking vendor performance against SOW, contracts and invoices to ensure consistency between work performed and contractual agreements Partner with Supply Chain to provide oversight and accountability of the applicable study drug(s), including supply projections, distribution, labeling and destruction Collaborate in the program‑level development of clinical strategies, goal‑setting, and establishment of timelines Required Skills and Experience BS/BA +12 / MS/MBA 8-10, PhD 5+ 5+ years direct clinical trial global experience (phase 2‑3 preferred) 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 human subject protection and the conduct of clinical trial (IRB, IND, etc.) Proven experience in the oversight 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 when decision making can occur at the study team level versus when 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 all levels Willingness to travel up to 25% of the time Employer identification code: 04050967. #J-18808-Ljbffr