Clinical Trial Manager

Clinical Trial Manager Location East Coast, United States of America Job Type Full-time Remote Remote Description Clinical Trial Manager | (Remote-Based) | Unique “Ground-Floor” Opportunity | Global Biotech | RETAINED SEARCH Cornerstone Search Group has been retained by an attractive, well-funded, and rapidly growing Global Biotech company that is expanding its presence here in the U.S. and building up its Clinical Operations team. This is an attractive ground-floor opportunity to get your foot in the door at a great time while they are still small, where you will be able to truly impact the continued growth and success of the company. Given the smaller company environment, our client is seeking someone who is flexible, creative-minded, enjoys rolling up their sleeves, and is comfortable working independently as part of a small team. As opposed to being a small fish in a big pond at a large organization, you will be a very visible and integral part of this company’s continued success and have the chance to impact from day one and grow internally. Location This is a remote-based position and the strong preference is for this person to live on the East Coast. Features ATTRACTIVE FEATURES ABOUT THIS COMPANY & OPPORTUNITY: Unique CTM Role: As our client is growing quickly and expanding its presence globally, you will play a key role in helping to build the company’s presence here, and serve as a key “face of the company” in the US. Visibility & Impact: As a smaller-sized company, they operate much leaner than Big Pharma, which will lend itself to more visibility/exposure, ability to truly impact, as well as internal growth opportunities. “Best of Both Worlds”: The company offers all the attractive features sought with a smaller clinical-stage Biotech (small team camaraderie, impact, agile, swift decision-making, minimal bureaucracy), while also getting the stability and financial security of an established parent company. Perfect Time to Join: This is an exciting time to join the company as they are starting to grow rapidly and expanding their Clinical Operations team globally. Great Company Culture: Work for a company that prides itself on having an excellent work culture - collaborative, autonomous, forward-thinking, creativity, and inclusive where people are engaged, enthusiastic, and have a patient-focused mindset. Responsibilities Accountable for the successful execution of all assigned projects measuring the results by on time, within budget, with high quality and in accordance with ICH-GCP and all applicable regulations. Works collaboratively with the Clinical Project Managers and clinical operations team to proactively drive project success. Support Global Clinical Operations Department by engaging, developing and maintaining relationships with clinical investigation sites. Build and cultivate key strategic relationships with investigators participating in the Company’s clinical studies and developing strategic clinical relationships with physicians/KOLs and key study site personnel. Develops standard study-level site budgets for clinical trials and works with the clinical operations team to ensure that the site-level budgets are consistent with the overall study budget. Ensure all trial deliverables are met according to timelines, budget, operational procedures and quality standards. Evaluate and oversee the activities required to execute, conduct, and complete clinical trials while managing to the established timelines and corporate budgets. Function as key liaison for vendor personnel, site personnel, and internal personnel regarding trial-related topics. Provide operational expertise to sites through ownership/management to ensure the engagement of highly motivated clinical investigators, which enables the company to maximize efficient and timely delivery of our clinical trials. Ensure collaboration with key internal & external stakeholders, as well as third party vendors. Qualifications / Requirements EDUCATION & DESIRED EXPERIENCE: A bachelor’s degree in a scientific or life sciences discipline. An advanced degree is a plus. 5+ years of relevant clinical trial experience in the pharmaceutical/biotech industry and proven experience in building/developing key relationships with Site Investigators/Physicians. Hands-on experience in a patient recruitment/enrollment capacity. Proven ability to work effectively in a fast-paced, entrepreneurial and creative environment. Ability and willingness to travel to sites. Ability to speak Spanish is a plus. Contact Brian Skurka Email: bskurka@cornerstonesg.com Phone: 973-656-0220x738 LinkedIn: https://www.linkedin.com/in/brianskurka1 Cornerstone Search Group, LLC 1200 Morris Turnpike | Short Hills, New Jersey 07078, USA www.cornerstonesg.com Recently Completed Retained Searches by Cornerstone Recently Completed Retained Searches by Cornerstone : Chief Medical Officer | Clinical-stage cell therapy biotech Chief Scientific Officer | Mid-size global biotech President/US Commercial Head | OSD Generics start-up VP, Oncology Drug Development | Early/later-stage oncology biotech VP, Global Clinical Operations | Clinical-stage biotech Head of Human Resources | Clinical-stage cell therapy biotech Head of Talent Acquisition| Clinical-stage rare disease biotech VP, Clinical Operations | Oncology start-up biotech ED, Clinical R&D, Oncology | Early-stage I-O biotech ED, Early Development, I-O | Top 10 Onc/I-O biopharma Senior Director, HR/Talent Acquisition | Cell therapy biotech Medical Director, Clinical Development Oncology Cornerstone's Privacy Policy Cornerstone Search Group considers all inquiries, resume submissions, and any other personal information submitted to us as confidential information. 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