Company Overview:

Protara Therapeutics is a clinical-stage biotechnology company committed to advancing transformative therapies for people with cancer and rare diseases. Protara’s portfolio includes its lead candidate, TARA-002, an investigational cell-based therapy in development for the treatment of non-muscle invasive bladder cancer (NMIBC) and lymphatic malformations (LMs). The Company is evaluating TARA-002 in an ongoing Phase 2 trial in NMIBC patients with carcinoma in situ (CIS) who are unresponsive or naïve to treatment with Bacillus Calmette-Guérin (BCG), as well as a Phase 2 trial in pediatric patients with LMs. Additionally, Protara is developing IV Choline Chloride, an investigational phospholipid substrate replacement for patients on parenteral support who are otherwise unable to meet their choline needs via oral or enteral routes.

Job Overview: 

The Director, Clinical Operations (CO), will provide leadership and oversight for clinical trial activities, ensuring operational efficiency, meeting global regulatory standards, as well as contributing to the overall success of Protara’s clinical programs. They will collaborate with internal stakeholders, clinical research organizations (CROs), vendors, and external parties (i.e., clinical site staff), as needed, to ensure the timely and cost-effective completion of clinical trials. They will be responsible for ensuring clinical trials are in compliance with Protara’s procedures, FDA regulations, and other applicable global regulations, GCP and ICH requirements.  They will strive to meet or beat Protara’s annual Corporate goals within the specified timelines and budget, with an emphasis on quality.

Essential Duties and Responsibilities include the following. Other duties may be assigned.

• Lead and mentor a team of CO professionals, fostering a culture of collaboration, accountability, and high performance.
• Drive process improvements, operational efficiencies, and risk management strategies within CO.
• Assess individual program needs in collaboration with VP, CO to ensure proper CO resourcing and budgeting across all Protara programs.
• Create and review CO Program timelines in Microsoft Project or Smartsheet.
• Work collaboratively with cross-functional teams (e.g., Clinical Science, Clinical Development, Program Management, Finance, Legal) to support clinical trial objectives.
• Lead the development of CO’s Standard Operating Procedures (SOP), Work Instructions (WI), training and other tools that will assist with onboarding new CO team members as well as inform current CO team on best practices.
• Provide feedback on relevant clinical documents (e.g., Protocols, Protocol Amendments, Informed Consent Forms (ICFs), Case Report Forms (CRFs), IRB/Ethics applications, recruitment materials, and other documents/plans, as applicable).
• Provide leadership in the development, implementation, and oversight of monitoring strategies for all Protara clinical trials.
• Ensure the integrity and quality of clinical trial data through periodic review of site’s data collection and performance.
• Perform or oversee co-monitoring visits to ensure the Clinical Research Organization’s (CRO) Clinical Research Associate’s (CRA) performance aligns with Protara’s expectations, ICH/GCP guidelines and the trial-specific monitoring plan.
• Assist with User Acceptance Testing (UAT) (e.g., MediData RAVE, eCOA, RTSM), as applicable.
• Provide clinical program updates, (e.g., trial status/metrics, budget, accomplishments and risks) to VP, CO, Senior Management and other relevant stakeholders.
• Participate in the oversight of global Regulatory submissions and approvals to Competent Authorities (CAs) and Ethical Committees (ECs).
• Represent Protara externally to Investigators, site staff, Key Opinion Leaders (KOLs).
• Assist with inspection readiness activities that support regulatory audits and inspections related to clinical trial conduct.

Education and/or Experience:

• Bachelor's degree in a scientific or health-related field is required.
• Master's degree in a scientific or health-related field is preferred.
• Minimum of 5-10 years of experience in clinical operations, with at least 5 years in a leadership role.
• Minimum of 5+ years of Non-Muscle Invasive Bladder Cancer (NMIBC) experience required.
• Demonstrated expertise in managing global clinical trials, from study design through regulatory submission and approval.
• Strong understanding of regulatory requirements and GCP guidelines.
• Proven track record of managing teams, vendors, and multi-disciplinary projects effectively.
• Experience in GCP inspections/audits required.

Supervisory Responsibilities:

• Clinical Trial Manager roles will be reporting into this position.

Computer Skills:

• Proficient in Microsoft (MS) Office Suite (e.g. Word, Excel, PowerPoint, Project).
• Experience with Smartsheet is preferred.

Certificates, Licenses, Registrations:

• PMP certification preferred.

 Other Skills and Abilities:

• Strong ability to prioritize tasks with keen attention to detail.
• Strong organizational, analytical, problem-solving, and communication skills.
• Must be a dependable self-starter and capable of working independently on multiple projects with the ability to prioritize tasks and meet deadlines.
• Thrives in a small biotech, fast-paced environment and enjoys working on multiple projects simultaneously.
• Strong interpersonal skills with the ability to interact effectively with all levels of Senior Management, both internal and external to the organization.

 Physical Demands:

The physical demands here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

 This position requires a minimal amount of travel; average travel for this position is 10-15% with some variation based upon the demands of the business imperatives. Travel will be needed for attending meetings, conferences, and site visits, as applicable.

 Work Environment:

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.

 Stable internet access is required.

*To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

*Salary Requirements are between $220,000 - $225,000 based on experience and qualifications.  We offer a competitive Compensation & Benefits package including incentive bonus, equity compensation, matching 401(k), medical, dental, vision, commuter, and fertility benefits.

Why You’ll Love Working at Protara 

• Friendly, open, and fun team-oriented culture that values unique & diverse perspectives.
• Company-wide dedication to profoundly impacting patients’ lives.
• Amazing culture whereby core values and behaviors are shared cross-functionally.
• Flexible working hours/schedule.
• Generous Paid Holidays and Unlimited PTO.

Protara was named one of the Best Places to Work by BioSpace, a leading industry news and job source. This honor demonstrates the company’s desirability in the recruitment marketplace, looking at various merits with an emphasis on culture, career growth and development opportunities, leadership and innovation.  Attracting and retaining top talent is integral to building a successful company in biotech, and we are committed to ensuring Protara provides our employees with an exceptional experience throughout their careers, even as we continue to grow.

 

Protara is committed to being a diverse and inclusive workplace. Protara is an Equal Opportunity Employer and is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, creed, religion, national or ethnic origin, citizenship status, age, sex or gender, gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information or any other characteristic protected by applicable federal, state or l