Job summary
Job post source
This job is from a recruiting firm hiring for a separate company
Job overview
The Senior CTA role involves supporting the clinical study team in planning, implementing, and completing studies, contributing significantly to the company's clinical operations.
Responsibilities and impact
Daily responsibilities include providing support to clinical study teams, managing clinical documents, maintaining regulatory compliance, and assisting with clinical trial logistics.
Compensation and benefits
The salary for this position ranges from $90,000 to $120,000, with benefits including medical, dental, vision, 401(k), telehealth services, ESOP, and commuter benefits.
Experience and skills
Candidates must have a minimum Bachelor's degree in a relevant scientific discipline and at least 2 years of experience in the pharma or biotech industry, specifically within clinical trials.
Company information
Clinical Resource Network (CRN), founded in 2002, provides clinical research and talent solutions for the pharmaceutical, biotech, and medical device industries, focusing on long-term relationships and various staffing solutions.
Job location and travel
This is a hybrid position based in South San Francisco, requiring 3 days onsite and 2 days remote with less than 25% travel.
Application process
Interested candidates are encouraged to apply if they meet the required qualifications.
Company overview
Clinical Resource Network (CRN) is a specialized organization providing comprehensive clinical trial support services to pharmaceutical, biotechnology, and medical device companies. They offer solutions such as patient recruitment, site management, and clinical monitoring to ensure efficient and effective clinical trials. CRN generates revenue by partnering with these companies to streamline the clinical trial process, thereby accelerating the development of new therapies and medical products. Founded with a focus on innovation and quality, CRN has established a reputation for reliability and excellence in the clinical research industry.
How to land this job
Position your resume to highlight your experience in clinical trials, especially your familiarity with eTMF and regulatory document management, as these are critical for the Senior CTA role at CRN.
Emphasize your ability to support clinical study teams, your experience with investigative sites and vendors, and your skills in tracking study-related activities and documents, as these align directly with the job responsibilities.
Apply through multiple platforms, including CRN's corporate site and LinkedIn, to enhance your chances of being noticed for this hybrid position.
Connect with professionals in the clinical team at CRN on LinkedIn to learn more about the company culture and specific expectations for the role; potential ice breakers could include asking about their recent projects or expressing interest in their approach to clinical trials.
Optimize your resume for ATS by integrating keywords from the job description such as 'clinical study support', 'eTMF', and 'regulatory documents' to improve your chances of passing initial screenings.
Utilizing Jennie Johnson's Power Apply feature can simplify your application process by ensuring your resume is tailored, identifying optimal channels for submission, and suggesting relevant LinkedIn connections to engage with, allowing you to focus more on your job search strategy.
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