Senior Director/Executive Director of Clinical Operations, Pulmovant

Pulmovant is a Roivant-backed clinical-stage biotechnology company developing innovative therapies for patients suffering from pulmonary diseases. Pulmovant’s first program, mosliciguat is designed to provide an effective, once-daily, inhaled treatment option for patients with pulmonary hypertension (PH). Mosliciguat is a novel, potential first-in-class, sGC activator with a differentiated mechanism that may have broad applicability across the PH spectrum.

Mosliciguat has been extensively characterized across a robust Phase 1 program with 170 participants dosed to date including patients with PH in the Phase 1b ATMOS study which has produced highly compelling and clinically meaningful efficacy data, as well as a favorable safety profile. Enrollment in a phase 2 trial is ongoing.

As part of the Roivant family of companies, Pulmovant leverages the power of collaboration and innovation to drive progress.

For more information, please visit https://www.pulmovant.com.

About Roivant:

Roivant specializes in developing transformative medicines at an accelerated pace through the launch of nimble biopharmaceutical and health technology entities, each meticulously tailored to address a specific medical need. Since its inception in 2014, Roivant has achieved the following critical milestones in support of its vision: built over 20 Vants; 12 consecutive positive Phase 3 trials; 8 FDA approvals; 5 successful IPOs; >$6B in capital raised; >$10B in global pharma partnerships and proceeds; and continued pipeline expansion across various modalities and therapeutic areas through in-licensing and acquisition of novel product candidates and technology platforms.  In addition to a robust clinical stage pipeline, Roivant also incubates discovery-stage companies and health technology startups complementary to its biopharmaceutical business.

Position: Senior Director/Executive Director of Clinical Operations, Pulmovant

Summary:

The SD/ED Clinical Operations will be responsible for leading critical programs for Pulmovant including taking lead of mosliciguat’s phase 3 program in Pulmonary Hypertension. S/he will lead and oversee execution and resourcing of the critical program. S/he will proactively identify and mitigate risks, lead from the front and collaborate with clinical development and operations teams to improve timelines, ensure operational planning and execution excellences, and budgeting for the clinical program. This is an opportunity to play an instrumental role in bringing a novel therapy to market with blockbuster commercial potential while providing better treatment options for patients living with pulmonary diseases. For the right candidate this could be a pathway to broader functional leadership responsibilities.

Responsibilities

• Responsible for clinical operations strategy, initiation, and execution of clinical trials, including (but not limited to) CRO/vendor selection, contracts & budgets, CRO/vendor oversight, and proactive risk management to ensure the quality conduct of trials with a high level of quality and data integrity

• Responsible for the successful planning and execution of Phase 2 and 3 trials

• Proactively builds and strengthens site and Investigator relationships and actively cultivates site engagement

• Work cross functionally to drive strategy, oversee the implementation of all clinical programs, and manage the integrated development plans to deliver against company goals

• Proactively identify potential risks and develop and implement actions and plans to avoid or mitigate program risks and make appropriate plan to balance risks, deliverables, and costs

• Lead and supervise all aspects of study progress from concept to close-out to assure adherence to intended timelines and achievement of study goals while ensuring quality in accordance with regulatory guidelines; heavy emphasis on late-stage development experience

• Develops and optimizes critical SOPs needed for program success, inspection readiness and compliance

• Oversee identification, qualification, and selection of CROs and vendors needed to conduct clinical trials including approval of Master Services Agreements and Task Orders with CRO

• Liaise with KOLs, Investigators, and clinical site staff to ensure optimal Sponsor-Site relationships

• Provide scientific/clinical expertise in the design and interpretation of clinical studies

• Ensure effective project or program communications and updates to internal and external stakeholders through meetings, presentations, and other methods

• Provide direct line management and training/mentoring of Clinical Operations team members

• Ensure clinical operation team are trained in regulatory inspection process and develop a pro-active approach for inspection readiness

• Align skills and resources needed for program success; work closely with internal and external stakeholders to leverage and optimize resources

• Create and oversee clinical program budget(s) and long-range clinical planning/forecasting activities

• Ensure there is proper oversight of identified safety concerns and/or adverse events; develop and implement corrective actions accordingly, and participate in internal/external study related audits, as needed

• Contribute as required to the authoring of key regulatory documents, study protocols, investigator’s brochures, IND reports, study postings, ensuring document and operating standards are established and maintained

• Participate in business development and process improvement/quality initiatives, as needed

Skills, Qualifications and Requirements

• Bachelor's Degree in a scientific discipline; with a minimum of 12-15 years clinical development experience.

• Extensive clinical operations management experience, including program leadership or TA leadership at a minimum

• Proven excellence in clinical operations strategy and execution, including Ph I-IV studies, global clinical trial operations, and multiple clinical trials simultaneously. Experience in Respiratory/Pulmonary diseases preferred

• Hands-on, detail-oriented leader with operational fluency

• Demonstrated ability to set and prioritize goals and objectives, excellent time management, negotiation, problem-solving and organizational skills

• Experience in building infrastructure (including SOPs) required

• Ability to work independently and collaboratively in a fast-paced, matrixed team environment consisting of internal and external team members

• Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines

• Strong leadership skills with ability to innovate and collaborate with a small team to articulate clear clinical strategy. Strong coaching and mentoring skills leading to the success and development of subordinates

• Willingness to work across all levels to support Clinical Operations success

• Strong communication and presentation skills

• Willingness/ability to travel (domestic and international)

Pulmovant provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

We will not accept unsolicited resumes nor outreach from agencies. Please do not send agency resumes to our website or Roivant Sciences and affiliated employees. Thanks!