Clinical Trial Manager, Vant (Remote)

Roivant’s mission is to systematically reduce the time, cost, and risk of delivering new medicines to market by accelerating the development of promising drug candidates to improve the lives of patients and their families. Since its inception in 2014, Roivant has achieved the following critical milestones in support of its vision: built over 20 portfolio companies (Vants); 5 successful IPOs; 10 consecutive positive phase 3 trials; 6 FDA approvals; >10$B in global pharma partnerships and proceeds; expanding pipeline of assets across various modalities and therapeutic areas; successful commercial launch of VTAMA®, (tapinarof) cream, 1%, for the topical treatment of plaque psoriasis in adults.  Building upon this track record of establishing a robust pipeline through in-licensing and acquisition of novel assets and technology platforms, Roivant is currently building new capabilities in drug discovery and expanding upon existing development disciplines to become the leading tech-enabled pharmaceutical company.

To learn more about our story and company culture, please visit us at https://roivant.com/

Position Summary:

The Clinical Operations Senior Clinical Trial Manager will work closely with the Director of Clinical Operations to help shape the development of the Vant’s lead clinical program. The scope of responsibilities for this role includes all aspects of trial planning and execution, timeline oversight, and vendor management. You will also be responsible for the preparation of study related materials, relationship management between clinical sites and vendors, and identification of project risks and contingency planning.   You will manage trials to the highest quality to ensure inspection readiness, timely and robust data collection, and assist the medical monitoring team with the maintenance of subject safety. 

Key Responsibilities:

• Work closely with the Director of Clinical Operations to manage operational study-level timeline, cost, and quality deliverables
• Lead the development of the clinical study plan including critical path activities
• Participate in CRO and Vendor Selection Process
• Oversee and drive clinical trial vendors, maintaining detailed understanding of timelines and tracking towards key study milestones
• Develop/update critical study documents as needed, including informed consent forms, study conduct documents such as study manuals, study tools, etc.; participate in development of protocols, investigator brochures, including updates and amendments Coordinate with the CRO to prepare/execute meetings including vendor kick off, study team meetings, regional team meetings, Investigator meetings and training
• Independently oversee CRO and vendor Clinical Study Plans to a quality completion, including Study Monitoring Plans, Site Selection Plans, Risk Management Plans, etc.
• Review CRO generated reports including monitoring visit reports, protocol deviation reports and site metrics reports to proactively identify and escalate areas of concern.
• Lead and conduct internal cross functional Study Team Meetings 
• Work closely and collaborate with internal cross functional colleagues to ensure early study milestones for regulatory submissions are met
• Triage, resolve, or escalate study issues/risks mitigations to the operations management team or additional stakeholders as appropriate
• Monitor study budget against trial progress and escalate deviations and reconcile with finance on an ongoing basis
• Mentor junior team members
• Coordinate and facilitate clinical document revisions (plans, memos, notes to file)
• Participate in any training meetings and train CROs/vendor staff as required
• Perform User Acceptance Testing for vendors and systems such as EDC, IRT, ePRO, etc
• Provides support to Clinical Operations team as needed

Requirements:

• Minimum 5-7 years experience in managing and leading clinical trial activities in global Phase 1-3 clinical trials with recent experience in study start up
• Bachelor’s degree or equivalent in the life sciences or related field required
• Experience in a small, fast-paced start up biotech is a plus
• Experience in indication is not required but is a plus
• Experience with CRO and vendor management; holding CRO and vendors accountable for timelines and milestones
• Must be willing to travel up to 25%, domestically and internationally to conferences, vendor meetings, and site visits.
• Ability to deal with multiple priorities and aggressive timelines
• Proven ability to independently manage multiple projects/tasks
• Strong Oral and written communication skills

Roivant Sciences 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!

Last updated on Aug 8, 2024