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- Tasks: Lead and mentor a team to oversee clinical site management and ensure successful trial execution.
- Company: Immunovant is a pioneering immunology company focused on innovative therapies for autoimmune diseases.
- Benefits: Enjoy remote work, unlimited paid time off, equity options, and comprehensive health benefits.
- Why this job: Join a dynamic team making a real impact in healthcare while working in a fast-paced environment.
- Qualifications: 15+ years in pharma with leadership experience; advanced degree preferred; strong knowledge of clinical trials.
- Other info: This role requires some travel (25%) and offers a collaborative, entrepreneurial culture.
The predicted salary is between 43200 - 72000 £ per year.
Senior Director, ROW Site Relationship Management (SRM)
Join to apply for the Senior Director, ROW Site Relationship Management (SRM) role at Immunovant
Senior Director, ROW Site Relationship Management (SRM)
Join to apply for the Senior Director, ROW Site Relationship Management (SRM) role at Immunovant
Direct message the job poster from Immunovant
Talent Acquisition/Recruiting partner hiring professionals and empowering people to change lives.#trailblazer
Immunovant, Inc. is a clinical-stage immunology company dedicated to enabling normal lives for people with autoimmune diseases. As trailblazer in anti-FcRn technology, the Company is developing innovative, targeted therapies to meet the complex and variable needs of people with autoimmune diseases.
Location: Remote (EN or CH based role)
The Role:
Reporting to the Vice President, Clinical Operations-GSM, this position is responsible to drives Immunovant’s ROW clinical site oversight in conjunction with Clinical Development, Clinical Operations, Medical Affairs and the CRO partner across all Immunovant clinical trial execution in the ROW. This role also partners these groups to define overall strategy toward achieving/exceeding program specific corporate targets, identifying and mitigating potential issues, and ensuring budget and timeline compliance. The incumbent will work with Clinical Operations and Quality to ensure the monitoring oversight program is running effectively. The role also involves direct supervision and mentoring of team members that reside across the ROW in their support of the clinical sites.
Key Responsibilities:
- Develop clinical site strategy for sites in the ROW including resourcing, budgeting, project plans, and oversight of sites in the ROW to achieve clinical program goals
- Will oversee the partnership with the Clinical Indications teams to collaboratively deliver program specific targets by ensuring seamless execution of team deliverables at the regional, country and site-specific levels.
- Lead a team of Immunovant ROW’ Site Relationship Managers that will assist clinical sites to ensure efficient study execution, answer questions and resolve issue
- Set strategy and lead the ROW Site Relationship Management team to execute study level recruitment plans by use of regional support group meetings and other related activities
- Lead the ROW Site Relationship Management team to support clinical sites in study execution from the Sponsor’s perspective and monitor oversight of the CRO’s CRAs. Activities include site feasibility, recommendations for selection, site start up support including SIV participation, enrollment booster activities, and ongoing logistical support to clinical sites throughout life of study.
- Per clinical site strategy recruit, hire, manage and mentor direct reports as required and support their professional development ensuring strong leadership and delivery through all levels of the team
- Partner with Patient Advocacy Director to ensure country specific plans are created to target appropriate national patient support/advocacy groups to target the ROW patient recruitment
- Partner with clinical operations and clinical development to provide proactive strategic and operational input for clinical development planning and execution that enables efficient delivery of high-quality clinical outcomes.
- Partner with Medical Liaison leadership to develop field-based strategy and to deliver on portfolio/clinical trial strategy at the regional/site level.
- Establish and report key performance indicators related to SRM site engagement and oversight activities.
- Ensure adherence to regulatory requirements (ICH, EMA, etc.) and GCP guidelines through establishment and reporting of clinical performance indicators KPIs/KQIs, and through innovative and agile methodology to improve processes. Ensure SRM adherence to the monitoring oversight plan and alignment with cross functional oversight plan, ensuring appropriate site escalations and assistance with remediations as needed.
- Ensure the lead SRM PM for each indication contributes to the preparation, and finalization of clinical protocols, PIS/ICFs, IB updates with any unique regional insights needed.
- Participate in RFP process and evaluation/selection process of CRO or other external vendor partners.
- In alignment with the clinical indication teams, the senior director ensures execution on enrollment plan, risk mitigation, issues management and delivery of high-quality data from the ROW’ sites.
- Provide input to the drafting of governance documents, SOPs, work instructions, and other resources.
- Leads and/or participates in initiatives for process, technology, or other continuous improvement to achieve cost-reduction, time-savings, efficiency, quality, or other business
- Build collaborative relationships with key internal stakeholders to facilitate the planning and execution of clinical trials, operational strategy, risk management and mitigation
- Within the Clinical Operations team, exhibit strong problem-solving skills and agility to adjust to changing business priorities and needs
- Collaborate cross-functionally, both internally and externally, to ensure highest quality customer service for clinical sites and patients. Support the SRMs as needed to ensure the necessary escalations occur for clinical sites in the ROW that have issues with CRO performance or support.
- Establish and nurture relationships with site investigators across the ROW’
Requirements:
- Bachelors in Life Sciences with an advanced degree preferred
- At least 15 years of experience in the pharmaceutical industry, with at least 10 years in a clinical leadership role on a cross-functional drug development project team (Biotech experience is a plus)
- PMP is a strong plus
- Global experience working across all phases of clinical research (Phases 1-4)
- Working knowledge of ICH and GCP regulations is required
- Understanding of regional cultural differences in a professional context (US vs EU)
- Experience in the use of industry Clinical Trial Management Systems and Clinical Trial Master File Systems or equivalent.
- Understanding of clinical trial operations and management of clinical trials at investigator sites
- Experience in rare disease therapeutic areas and patient engagement strategies preferred
- Direct supervisory experience
- Unrelenting dedication to delivering quality results
- Integrity, in word and action
- Willingness to roll up your sleeves and get in the weeds of projects as a jack of all trades
- Ability to think outside of the box and challenge the status quo
- Natural entrepreneurial spirit with unrelenting dedication to delivering results
- Desire to work in a fast-paced, innovative environment
- Natural collaborator who enjoys working on a cross-functional team
- Location: Remote (EN or CH based role)
- Dynamic, interactive, fast-paced, and entrepreneurial environment
- Domestic or international travel are required (25%)
Salary range for posting
Compensation is based on a number of factors, including market location, and may vary depending on job-related knowledge, skills, and experience. Equity and other forms of compensation may be provided as part of a total compensation package, in addition to a full range of medical, dental, vision, 401k, and other benefits, including unlimited paid time off and parental leave.
Seniority level
-
Seniority level
Director
Employment type
-
Employment type
Full-time
Job function
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Job function
Project Management, Management, and Other
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Senior Director, ROW Site Relationship Management (SRM) employer: Immunovant
Contact Detail:
Immunovant Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Director, ROW Site Relationship Management (SRM)
✨Tip Number 1
Network with professionals in the clinical research field, especially those who have experience in ROW site management. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends in clinical operations.
✨Tip Number 2
Familiarise yourself with Immunovant's specific therapeutic areas and their approach to autoimmune diseases. Understanding their unique strategies will help you articulate how your experience aligns with their goals during discussions.
✨Tip Number 3
Prepare to discuss your leadership style and how you've successfully managed cross-functional teams in the past. Highlight specific examples where you've driven results in clinical trial execution, as this will resonate well with the hiring team.
✨Tip Number 4
Stay updated on regulatory requirements and best practices in clinical trial management. Being knowledgeable about ICH and GCP guidelines will demonstrate your commitment to quality and compliance, which is crucial for this role.
We think you need these skills to ace Senior Director, ROW Site Relationship Management (SRM)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical leadership and project management. Emphasise your understanding of ICH and GCP regulations, as well as any specific achievements in the pharmaceutical industry that align with the role.
Craft a Compelling Cover Letter: In your cover letter, express your passion for immunology and how your background makes you a perfect fit for the Senior Director role. Mention specific experiences that demonstrate your ability to lead cross-functional teams and manage clinical trials effectively.
Highlight Leadership Experience: Clearly outline your direct supervisory experience and your approach to mentoring team members. Provide examples of how you've successfully led teams in achieving clinical program goals and overcoming challenges.
Showcase Problem-Solving Skills: Include examples in your application that illustrate your strong problem-solving skills and agility in adapting to changing business priorities. This will show Immunovant that you can thrive in their dynamic environment.
How to prepare for a job interview at Immunovant
✨Understand the Role Thoroughly
Before the interview, make sure to read the job description carefully. Familiarise yourself with the key responsibilities and requirements of the Senior Director, ROW Site Relationship Management role. This will help you tailor your answers to demonstrate how your experience aligns with what Immunovant is looking for.
✨Showcase Your Leadership Experience
As a senior director, you'll need to exhibit strong leadership skills. Prepare examples from your past roles where you've successfully led teams, managed projects, or navigated challenges in clinical operations. Highlight your ability to mentor and develop team members, as this is crucial for the position.
✨Demonstrate Cultural Awareness
Given the global nature of the role, it's important to show an understanding of regional cultural differences. Be ready to discuss how you've adapted your strategies or communication styles when working with diverse teams or stakeholders across different regions.
✨Prepare Questions for the Interviewers
Interviews are a two-way street. Prepare insightful questions that show your interest in Immunovant's mission and the specific challenges they face in clinical trial execution. This not only demonstrates your enthusiasm but also helps you assess if the company culture and values align with yours.