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Clinical Science Liaison
Precision BioSciences, Inc.Clinical Science Liaison at Precision BioSciences managing clinical trial relationships for PBGENE-DMD. Interface with clinical sites and advocacy communities for effective trial support.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical research and patient advocacy, with a strong focus on managing clinical trial site relationships and engaging with patient advocacy organizations. Proficient in scientific communication and training, with a commitment to improving patient journey experiences in clinical trials.
Highest-signal resume keywords
Clinical Research ExperiencePediatric Rare Disease ExpertisePatient Advocacy EngagementScientific Communication SkillsClinical Trial Site Relationship Management
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical ResearchMedical AffairsPatient AdvocacyClinical PracticeProtocol TrainingData TranslationSite Operations ManagementRecruitment SupportInvestigator EngagementTherapeutic Area Knowledge
Soft Skills
Communication SkillsTeam CollaborationTraining and EducationRelationship ManagementProblem-Solving
Certifications & Qualifications
Bachelor's Degree
Industry Keywords
BiotechPharmaClinical TrialsNeuromuscular TherapeuticsPatient CommunitiesClinical DevelopmentClinical OperationsCRO LiaisonSite-Level TrainingPatient Journey
About the role
Key responsibilities & impact- Serve as a primary scientific interface site-level contact for investigators and site medical staff within responsible geography
- liaising with Clinical Operations, the CRO and the Medical Monitor who maintain primary contacts for site operations
- Lead site-level training on protocol procedures and staff support
- Understand the patient journey in the trial at the clinical site and work with staff to facilitate improvements
- Meet with all staff who will be assessing patients to ensure consistency with assessments
- Educate staff about PBGENE-DMD; Train fellows & residents that cycle through the clinical site
- Provide frequent updates to Clinical team to support ongoing recruitment
- Partner with Clinical Development, Clinical Operations, Program Management and Corporate Communications team to support compliant scientific education for advocacy organizations and patient communities
- Support investigator engagement and relationship management alongside Clinical Development leadership
Requirements
What you’ll need- Bachelor's degree (or equivalent) and 7+ years of total experience in clinical research, medical affairs, patient advocacy, or clinical practice within biotech, pharma, and/or clinical trial site(s), or equivalent combination of education and experience
- Direct experience in pediatric rare disease or neuromuscular therapeutic areas
- Demonstrated experience managing clinical trial site relationships
- Track record of engagement with patient advocacy organizations
- Strong scientific communication skills; ability to translate complex data for diverse audiences
- Willingness to travel up to 60-70% at peak
Benefits
Comp & perks- Health insurance
- 401(k) matching
- Flexible work hours
- Paid time off
- Remote work options