In-House Clinical Research Associate II / Senior In-House CRA
Posted 20 days ago
Job summary
Job post source
This job is directly from Precision For Medicine
Job overview
The In-House Clinical Research Associate II / Senior In-House CRA at Precision For Medicine supports clinical research studies by assisting study sites and project teams, ensuring compliance with protocols and regulations, and acting as a key contact for study sites.
Responsibilities and impact
The role involves supporting investigator recruitment, managing study documentation and site data, coordinating meetings, assisting with regulatory submissions, tracking study progress, supporting site visits, and mentoring junior staff, all while ensuring compliance with ICH-GCP and company SOPs.
Compensation and benefits
The estimated salary range is $66,241 to $99,362 USD, with compensation based on skills, experience, and other factors; benefits include adherence to privacy policies and equal opportunity employment practices.
Experience and skills
Candidates need a bachelor's degree or equivalent, at least 2 years of relevant experience, proficiency in Microsoft Office, strong communication skills, knowledge of drug development, and ability to travel; preferred qualifications include clinical research experience, organizational skills, and remote work capability.
Career development
The position offers opportunities to mentor junior staff and gain experience in various clinical research activities, supporting professional growth within the company.
Work environment and culture
Precision For Medicine values professionalism, teamwork, flexibility, and adherence to regulatory standards, promoting a detail-oriented and collaborative work environment with options for remote work.
Company information
Precision For Medicine is a clinical research organization focused on supporting clinical studies with a commitment to regulatory compliance and quality standards, emphasizing equal opportunity employment and data privacy.
Team overview
The candidate will join a study team working independently with minimal supervision, collaborating with project members and supporting site management and monitoring activities.
Application process
Applicants are informed about privacy policies and accommodations for disabilities; the company warns against fraudulent offers and emphasizes a formal interview process through their recruiting team.
Unique job features
The role includes unique responsibilities such as mentoring new graduates, supporting both remote and on-site activities, and using Clinical Trial Management Systems for study tracking.
Company overview
Precision for Medicine is a global company specializing in supporting life sciences companies in the development and commercialization of new treatments. They provide comprehensive services that include clinical trial management, data analytics, and laboratory services, focusing on precision medicine to tailor treatments to individual patients. The company generates revenue through contracts with pharmaceutical and biotechnology firms, offering expertise in regulatory affairs, biomarker discovery, and patient engagement. Founded in 2012, Precision for Medicine has grown significantly through strategic acquisitions and partnerships, establishing a robust presence in the personalized healthcare sector.
How to land this job
Tailor your resume to highlight your knowledge and application of ICH-GCP guidelines, clinical trial management, and regulatory compliance, as these are core to the In-House CRA II role at Precision For Medicine.
Emphasize your experience in site management tasks such as document collection, site feasibility assessments, investigator support, and use of clinical systems like CTMS and EDC, reflecting the detailed responsibilities in the job description.
Apply through multiple channels including Precision For Medicine’s official careers page, LinkedIn, and reputable clinical research job boards to maximize your application’s reach.
Connect with current In-House CRAs or clinical project team members at Precision For Medicine on LinkedIn; use ice breakers like commenting on recent clinical trials they supported or asking about best practices for remote site management.
Optimize your resume for ATS by incorporating keywords from the job description such as 'ICH-GCP,' 'clinical trial management system,' 'investigator site files,' 'site feasibility,' and 'regulatory compliance' to ensure your resume passes automated screenings.
Use Jennie Johnson's Power Apply feature to automate tailoring your resume, applying through multiple platforms, and identifying LinkedIn contacts to network with, freeing you to focus on interview preparation and follow-up.
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