Job Description
Our mission is to empower healthcare and life science companies by providing expertise in
sourcing and placing top clinical research professionals across a
multitude of diverse opportunities. We have a proven track record with
pharmaceutical, biotechnology, diagnostic, medical device, and CRO
customers. Leading companies have chosen us as their preferred
partner for its quality of customer service, excellent candidate
profile, and its long-term relationships.
Exciting and unique CTM role our Client is an innovative
biopharmaceutical company specializing in cutting-edge cancer
treatments. They have received a prestigious Innovation Award in 2020
for their groundbreaking drug delivery technology.
Their pioneering platform aims to improve patient survival and
quality of life by refining the chemotherapy process and making it more
specific. They hold FDA Orphan Drug Designation for two cancer types,
providing market exclusivity. Their mission is to expand their portfolio
of targeted therapies, elevating care standards for solid tumor
patients.
Our Client is searching for a Clinical Trial Manager (CTM) with an
entrepreneurial spirit, curiosity, and keen attention to detail. You'll
play a vital role in bridging departments, finding solutions, and
advancing our team, patient care, and mission. Leading with empathy and
humility, you'll contribute to our growth while staying dedicated to
effective cancer treatments. If you share these values and consider
yourself a hands-on CTM, our recruiter would like to speak with
you.
Responsibilities
As a CTM you will come to the Los Altos office and act as a vital
contributor to fostering our client's culture, ensuring accountability,
and managing daily clinical team operations. With this company, you
will collaborate with the management team to translate their clinical
strategy into actionable short-term plans and ensure their successful
execution to meet their annual and long-term corporate goals. This
position is suited for someone well-versed in the dynamic clinical
landscape, capable of immediate action, and adept at identifying and
addressing issues.
- Hands on CTM with a keen ability to manage all aspects of clinical development.
- Have command over submissions and communications with IRBs and ECs
- Create study/program milestones with well-developed tracking and reporting.
- Work with minimal supervision and open to people management and training.
- Have a strong understanding and ability to manage multi-center oncology trials.
- Create and complete Informed Consent Forms (ICFs), protocols
and amendments, Investigator's Brochure (IB), site budget and Clinical
Trial Agreement (CTA), and make valuable contributions to IND
submissions
Qualifications
- Bachelor’s degree, RN or equivalent
- Minimum of 6-8 years of experience in clinical research; oncology experience preferred.
- Demonstrates strong analytical, technical, and project
management skills, excelling under pressure and juggling competing
priorities.
- Highly experienced with senior executives in both large pharma
and emerging biotech. A resourceful, strategic, and analytical thinker,
skilled in shaping future company strategy, anticipating challenges,
and devising successful solutions.
* Please note, that the compensation offered to the final candidate
depends on relevant work experience, skills, and years of experience.
Benefits
We are an Equal Opportunity Employer and prohibit discrimination and harassment of any kind.