Gilead
Associate Director- Clinical Site Partner (Inflammation)
Gilead, Atlanta, Georgia, United States, 30383
Employer Industry: Biotechnology
Why consider this job opportunity: - Salary up to $230,230.00 - Eligible for a discretionary annual bonus and stock-based long-term incentives - Comprehensive benefits package including medical, dental, vision, and life insurance - Opportunity for career advancement and growth within the organization - Work in a collaborative environment that values inclusion and diverse perspectives - Engage directly with clinical trial processes and make a significant impact on patient care
What to Expect (Job Responsibilities): - Establish and maintain strong professional relationships with investigator sites to optimize clinical trial program delivery - Develop strategies for concierge-level support for preferred sites, enhancing Gilead's reputation as a Sponsor of Choice - Track and assess site performance metrics to identify opportunities for improvement - Serve as an internal resource to advocate for patient perspectives throughout the product development process - Collaborate with internal teams to ensure effective communication and support for clinical trial execution
What is Required (Qualifications): - Located in Southeast Florida or Georgia - BA/BS/RN with 10+ years of relevant clinical or related experience in life sciences, or MA/MS/PharmD/PhD with 8+ years of experience - Strong knowledge of Good Clinical Practice and in-country regulatory guidelines - Scientific/medical expertise in a relevant therapeutic area and advanced knowledge of Clinical Operations - Proven ability to manage workload, set priorities, and work both independently and collaboratively
How to Stand Out (Preferred Qualifications): - Prior experience with inflammation clinical trials in company-sponsored settings - Excellent verbal and written communication skills in English and local language - Strong leadership presence with the ability to lead without formal authority - Exceptional negotiation and conflict resolution skills - Self-motivated with proactive issue monitoring and problem-solving capabilities
#Biotechnology #ClinicalTrials #PatientCare #CareerOpportunity #Leadership #DiversityInclusion
"We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately. We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer."
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Why consider this job opportunity: - Salary up to $230,230.00 - Eligible for a discretionary annual bonus and stock-based long-term incentives - Comprehensive benefits package including medical, dental, vision, and life insurance - Opportunity for career advancement and growth within the organization - Work in a collaborative environment that values inclusion and diverse perspectives - Engage directly with clinical trial processes and make a significant impact on patient care
What to Expect (Job Responsibilities): - Establish and maintain strong professional relationships with investigator sites to optimize clinical trial program delivery - Develop strategies for concierge-level support for preferred sites, enhancing Gilead's reputation as a Sponsor of Choice - Track and assess site performance metrics to identify opportunities for improvement - Serve as an internal resource to advocate for patient perspectives throughout the product development process - Collaborate with internal teams to ensure effective communication and support for clinical trial execution
What is Required (Qualifications): - Located in Southeast Florida or Georgia - BA/BS/RN with 10+ years of relevant clinical or related experience in life sciences, or MA/MS/PharmD/PhD with 8+ years of experience - Strong knowledge of Good Clinical Practice and in-country regulatory guidelines - Scientific/medical expertise in a relevant therapeutic area and advanced knowledge of Clinical Operations - Proven ability to manage workload, set priorities, and work both independently and collaboratively
How to Stand Out (Preferred Qualifications): - Prior experience with inflammation clinical trials in company-sponsored settings - Excellent verbal and written communication skills in English and local language - Strong leadership presence with the ability to lead without formal authority - Exceptional negotiation and conflict resolution skills - Self-motivated with proactive issue monitoring and problem-solving capabilities
#Biotechnology #ClinicalTrials #PatientCare #CareerOpportunity #Leadership #DiversityInclusion
"We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately. We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer."
#J-18808-Ljbffr