EPM Scientific - Phaidon International
Clinical Study Lead (Sr. Clinical Research Associate)
EPM Scientific - Phaidon International, San Francisco, California, United States, 94199
Salary: $120-130KCompany Summary:
A global, specialty pharmaceutical group with an impressive track record is seeking a motivated Clinical Study Lead for a hybrid role in San Francisco (Palo Alto). Their commercial supply of pharmaceutical products generated $83m in revenue in FY2023 (a 24% uptick from the year prior during a year of record layoffs). Since their first clinical trials in 2006, they've had 3 approvals already on the market. Currently, they have 6 indications in Phases II and III, so they are looking for a driven, growth-oriented Clinical Study Lead to drive their pipeline forward.***** Candidate must be based in SF to be considered.*****The Clinical Study Lead will be responsible for:Leading in house study activities studies for a large global Ph. 3 studyMentoring junior team membersOverseeing the set-up and maintenance of study systems which may include Clinical Trial Management System (CTMS), Trial Master File (TMF), study SharePoint etc.Reporting into the Clinical Program LeadMay be responsible for CRA and CTAs as direct reportsAn ideal candidate for this role MUST have…5+ years of sponsor/CRO experience3+ years of ON-SITE monitoring experience2+ years of experience leading studies or trials in house (rare disease or derm preferred)At least 2 years of experience managing direct reports or mentoring junior clin ops team membersA Bachelor's degree in Biological Sciences, Nursing, Pharmacy or a related disciplineA working knowledge of ICH GCP guidelinesBenefits:Competitive salary with benefitsHigh degree of commercial exposure early in your careerBeing a part of team whose work directly aims to improve the quality of people's livesGreat work-life balanceIf you are interested in this Clinical Study Lead role, don't hesitate to reach out!
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A global, specialty pharmaceutical group with an impressive track record is seeking a motivated Clinical Study Lead for a hybrid role in San Francisco (Palo Alto). Their commercial supply of pharmaceutical products generated $83m in revenue in FY2023 (a 24% uptick from the year prior during a year of record layoffs). Since their first clinical trials in 2006, they've had 3 approvals already on the market. Currently, they have 6 indications in Phases II and III, so they are looking for a driven, growth-oriented Clinical Study Lead to drive their pipeline forward.***** Candidate must be based in SF to be considered.*****The Clinical Study Lead will be responsible for:Leading in house study activities studies for a large global Ph. 3 studyMentoring junior team membersOverseeing the set-up and maintenance of study systems which may include Clinical Trial Management System (CTMS), Trial Master File (TMF), study SharePoint etc.Reporting into the Clinical Program LeadMay be responsible for CRA and CTAs as direct reportsAn ideal candidate for this role MUST have…5+ years of sponsor/CRO experience3+ years of ON-SITE monitoring experience2+ years of experience leading studies or trials in house (rare disease or derm preferred)At least 2 years of experience managing direct reports or mentoring junior clin ops team membersA Bachelor's degree in Biological Sciences, Nursing, Pharmacy or a related disciplineA working knowledge of ICH GCP guidelinesBenefits:Competitive salary with benefitsHigh degree of commercial exposure early in your careerBeing a part of team whose work directly aims to improve the quality of people's livesGreat work-life balanceIf you are interested in this Clinical Study Lead role, don't hesitate to reach out!
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