Clinical Research Associate II - Full Service - Oncology (Home-Based in Central US)

Syneos Health/ inVentiv Health Commercial LLC; Arkansas; Remote; USD 60,000 - 80,000; Full time

Job summary

A leading biopharmaceutical solutions organization is seeking a Clinical Research Associate II to conduct monitoring of clinical studies. This role requires 2-4 years of experience in clinical research, strong GCP knowledge, and excellent communication skills. Join a team dedicated to quality monitoring and clinical trial success, with benefits including health coverage and a company car allowance.

Benefits

Company car or car allowance

Health benefits (Medical, Dental, Vision)

401k company match

Employee Stock Purchase Plan

Flexible paid time off

Qualifications

• 2-4 years of experience in clinical research monitoring.
• Strong knowledge of Good Clinical Practice (GCP) guidelines.
• Excellent communication and interpersonal skills.

Responsibilities

• Conduct on-site and remote monitoring of clinical research studies.
• Develop and implement tools, procedures, and processes for quality monitoring.
• Manage components of projects within the area of responsibility.

Skills

Attention to detail

Strong analytical skills

Problem-solving abilities

Effective teamwork

Strong organizational skills

Time management skills

Education

Bachelor's degree in a related field or equivalent experience

Tools

Clinical trial management systems

Microsoft Office Suite

Job description

Overview

Clinical Research Associate II - Full Service - Oncology (Home-Based in Central US)

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you''ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:

Why Syneos Health

• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
• We are continuously building the company we all want to work for and our customers want to work with. When we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we''re able to create a place where everyone feels like they belong.

Job Responsibilities

• Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms
• Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates
• Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials
• Manage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues
• Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and action plans
• Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct

Qualifications

• Bachelor's degree in a related field or equivalent experience
• Minimum of 2-4 years of experience in clinical research monitoring
• Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements
• Excellent communication and interpersonal skills
• Ability to work independently and manage multiple priorities
• Proficiency in using clinical trial management systems and other relevant software

Certifications

• Certified Clinical Research Associate (CCRA) or equivalent certification preferred

Necessary Skills

• Attention to detail and strong analytical skills
• Problem-solving abilities and critical thinking
• Ability to work effectively in a team environment
• Strong organizational and time management skills
• Proficiency in Microsoft Office Suite

Benefits and Additional Information

At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. The benefits for this position may include a company car or car allowance, health benefits (Medical, Dental, Vision), company match 401k, eligibility to participate in the Employee Stock Purchase Plan, eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Paid sick time eligibility may vary by location. Syneos complies with applicable paid sick time requirements.

Salary Range: The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on qualifications, skills, competencies, and role proficiency.

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 studies across many sites and trial patients.

Additional information: Tasks and responsibilities are not exhaustive. The Company may assign other tasks as needed. This description is intended to comply with applicable laws and company policies.