Senior Level Clinical Associate Jobs
Senior level clinical associate jobs place experienced professionals in charge of clinical programs, cross-functional initiatives, and the teams that carry them forward. Most openings are on-site, remote, or hybrid across Biotechnology & Pharmaceuticals, Education, and Healthcare & Medical Services, with employers like University Of Washington, Revolution Medicines, and Jobot hiring at this level now.
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Job Summary:
The Associate Director, Clinical Development will support the advancement of Revance therapeutics products and indications through the design and execution of Phase 1-3 clinical studies. This role will contribute to clinical program strategy, study design, protocol development, and regulatory submissions to support expanded therapeutic applications. Responsibilities also include developing clinical and scientific content for publications and presentations, participating in regulatory meetings and scientific conferences, engaging with external KOLs, and partnering closely with internal stakeholders, Clinical Operations, and CROs to support successful study execution.
Reporting to: VP, Clinical Development & Data Science
Location: Nashville, TN preferred; remote for highly qualified candidates
- this role will require ~30% travel
Responsibilities/Essential Duties:
- Develop scientific methods, design clinical studies, and develop and implement clinical protocols.
- Gather internal and external feedback on clinical research programs.
- Be accountable for study protocols in collaboration with Biometrics, Clinical Operations, Safety, and Medical Affairs groups.
- Represent clinical research through membership on trial teams.
- Recruit, guide, and motivate clinical investigators.
- Support Data Monitoring Committees and Data Safety Monitoring Boards with presentations.
- Author relevant sections of protocols, Clinical Study Reports, investigator brochures, IND/BLA submissions, and other clinical/regulatory/safety documents.
- Regularly report to clinical development and scientific leadership.
- Ensure study compliance by understanding and applying all relevant SOPs and GCPs.
- Present technical information to internal teams; represent Revance externally through publications and presentations at scientific meetings and congresses.
- Participate in long-range strategic product planning for current and future products.
Basic Qualifications:
- Advanced Degree & 7-10 years' directly related experience.
Preferred Qualifications:
- MD, DO, PhD, PharmD, or other recognized doctorate-level education.
- 7-10+ years' experience in the design, execution, and evaluation of clinical trials, with an emphasis on phases 2-4.
- Recent track record of successful IND and (s)NDA/BLA submissions.
- Responsibility for physician-sponsored or company-sponsored clinical trials.
- In-depth understanding of pharmaceutical regulatory requirements and their impact on development of clinical trials and NDA/BLA submissions.
- An active network within Neurology or Physiatry. This will include KOLs, key research centers, patient advocacy groups, and a variety of patient care organizations.
- Able to write clearly and succinctly in a variety of communication settings. Open, transparent, and succinct communication skills.
- Experience working with corporate/academic partners and contract research organizations.
- Excellent communication skills, both written and verbal.
- Effective team member with outstanding interpersonal skills.
- Ability to develop project strategies and execute project details.
- Demonstrated ability to function effectively in a corporate environment while maintaining the highest ethical, regulatory, and scientific standards.
- Highly developed problem-solving capabilities.
- Ability to effectively learn and convey clinical and non-clinical technical information.
- Strong presentation and teaching skills.
- Ability to work independently and with cross-functional teams.
- Strong organizational and time-management skills, with the ability to manage multiple complex projects.
- Strong data analysis capabilities.
- Ability to travel up to 30%.
Company Summary:
Revance is a global company developing, producing, and distributing industry-leading, differentiated products across aesthetics, skincare, and therapeutics. Revance drives innovation beyond convention to offer treatment options for individuals across generations. The Company's vision is to redefine excellence in aesthetics, skincare, and therapeutics through science-powered innovation, with an unwavering commitment to its providers, patients, and consumers. Revance's award-winning products are the result of robust research and development, a cornerstone for the Company, driven by renowned scientists.
What Revance invests in you:
- Competitive Compensation including base salary and annual performance bonus.
- Flexible PTO, holidays, and parental leave.
- Generous healthcare benefits, HSA match, 401k match, employer paid life and disability insurance, pet insurance, wellness discounts and much more!
This section of the job description is required by the American with Disability Act (ADA). The ADA requires that job descriptions reflect the physical and mental demands required to effectively perform the essential duties of the job. The ADA prohibits employers from discriminating against a "qualified individual with a disability" in all aspects of the employment relationship. A "qualified individual with a disability" is "an individual who meets the education, experience, skill, and other job-related requirements of a position held or desired, and who, with reasonable accommodation, can perform the essential functions of a specified job."
Revance is an Equal Opportunity employer. All qualified applicants will receive consideration for employment based on merit, without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
Job Summary:
The Associate Director, Clinical Development will support the advancement of Revance therapeutics products and indications through the design and execution of Phase 1-3 clinical studies. This role will contribute to clinical program strategy, study design, protocol development, and regulatory submissions to support expanded therapeutic applications. Responsibilities also include developing clinical and scientific content for publications and presentations, participating in regulatory meetings and scientific conferences, engaging with external KOLs, and partnering closely with internal stakeholders, Clinical Operations, and CROs to support successful study execution.
Reporting to: VP, Clinical Development & Data Science
Location: Nashville, TN preferred; remote for highly qualified candidates
- this role will require ~30% travel
Responsibilities/Essential Duties:
- Develop scientific methods, design clinical studies, and develop and implement clinical protocols.
- Gather internal and external feedback on clinical research programs.
- Be accountable for study protocols in collaboration with Biometrics, Clinical Operations, Safety, and Medical Affairs groups.
- Represent clinical research through membership on trial teams.
- Recruit, guide, and motivate clinical investigators.
- Support Data Monitoring Committees and Data Safety Monitoring Boards with presentations.
- Author relevant sections of protocols, Clinical Study Reports, investigator brochures, IND/BLA submissions, and other clinical/regulatory/safety documents.
- Regularly report to clinical development and scientific leadership.
- Ensure study compliance by understanding and applying all relevant SOPs and GCPs.
- Present technical information to internal teams; represent Revance externally through publications and presentations at scientific meetings and congresses.
- Participate in long-range strategic product planning for current and future products.
Basic Qualifications:
- Advanced Degree & 7-10 years' directly related experience.
Preferred Qualifications:
- MD, DO, PhD, PharmD, or other recognized doctorate-level education.
- 7-10+ years' experience in the design, execution, and evaluation of clinical trials, with an emphasis on phases 2-4.
- Recent track record of successful IND and (s)NDA/BLA submissions.
- Responsibility for physician-sponsored or company-sponsored clinical trials.
- In-depth understanding of pharmaceutical regulatory requirements and their impact on development of clinical trials and NDA/BLA submissions.
- An active network within Neurology or Physiatry. This will include KOLs, key research centers, patient advocacy groups, and a variety of patient care organizations.
- Able to write clearly and succinctly in a variety of communication settings. Open, transparent, and succinct communication skills.
- Experience working with corporate/academic partners and contract research organizations.
- Excellent communication skills, both written and verbal.
- Effective team member with outstanding interpersonal skills.
- Ability to develop project strategies and execute project details.
- Demonstrated ability to function effectively in a corporate environment while maintaining the highest ethical, regulatory, and scientific standards.
- Highly developed problem-solving capabilities.
- Ability to effectively learn and convey clinical and non-clinical technical information.
- Strong presentation and teaching skills.
- Ability to work independently and with cross-functional teams.
- Strong organizational and time-management skills, with the ability to manage multiple complex projects.
- Strong data analysis capabilities.
- Ability to travel up to 30%.
Company Summary:
Revance is a global company developing, producing, and distributing industry-leading, differentiated products across aesthetics, skincare, and therapeutics. Revance drives innovation beyond convention to offer treatment options for individuals across generations. The Company's vision is to redefine excellence in aesthetics, skincare, and therapeutics through science-powered innovation, with an unwavering commitment to its providers, patients, and consumers. Revance's award-winning products are the result of robust research and development, a cornerstone for the Company, driven by renowned scientists.
What Revance invests in you:
- Competitive Compensation including base salary and annual performance bonus.
- Flexible PTO, holidays, and parental leave.
- Generous healthcare benefits, HSA match, 401k match, employer paid life and disability insurance, pet insurance, wellness discounts and much more!
This section of the job description is required by the American with Disability Act (ADA). The ADA requires that job descriptions reflect the physical and mental demands required to effectively perform the essential duties of the job. The ADA prohibits employers from discriminating against a "qualified individual with a disability" in all aspects of the employment relationship. A "qualified individual with a disability" is "an individual who meets the education, experience, skill, and other job-related requirements of a position held or desired, and who, with reasonable accommodation, can perform the essential functions of a specified job."
Revance is an Equal Opportunity employer. All qualified applicants will receive consideration for employment based on merit, without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
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Find JobsSenior Level Clinical Associate Job Market
Who's Hiring
- Revolution Medicines13
- University Of Washington10
- Jobot4
- PTC Therapeutics4
Top Industries Hiring
- Biotechnology & Pharmaceuticals26
- Education10
- Healthcare & Medical Services6
- Staffing & Recruiting4
- Science & Research2
Senior Level Clinical Associate Jobs: Frequently Asked Questions
How do I get a senior level clinical associate job?
Employers at this level look for demonstrated ownership of clinical workflows, protocols, or programs rather than task execution. Candidates who have led cross-functional projects, mentored junior staff, or driven measurable process improvements stand out. Tailoring your application to show scope of responsibility and decision-making authority gives you a clear edge over those who only list duties.
Which companies hire senior level clinical associates?
Companies hiring senior level clinical associates right now include University Of Washington, Revolution Medicines, and Jobot, based on current listings on Migrate Mate as of November 2026. Hiring at this level tends to come from established health systems, pharmaceutical and medical device companies, and large research or academic medical centers with ongoing clinical programs.
Are there remote senior level clinical associate jobs?
Yes, though availability varies by specialty and employer. About 18% of senior level clinical associate openings are remote or hybrid as of November 2026, with fully remote roles more common in clinical operations, data oversight, and regulatory affairs than in hands-on patient-facing or laboratory settings.
What makes a clinical associate role senior level?
Senior level clinical associate roles carry broader ownership than mid level positions. Expectations typically include leading clinical studies or programs end to end, serving as a subject matter resource for less experienced colleagues, contributing to protocol design or standard operating procedures, and coordinating across departments without close day-to-day supervision. The defining shift is from executing tasks to setting standards and driving outcomes.
Which industries hire the most senior level clinical associates?
Senior Level clinical associate roles concentrate in Biotechnology & Pharmaceuticals, Education, and Healthcare & Medical Services, based on current listings on Migrate Mate as of November 2026. These sectors drive hiring at this level because they run complex, multi-site clinical programs that require experienced professionals who can manage compliance, timelines, and stakeholder coordination independently.