Senior CRA I – Sponsor Dedicated

🕒 February 4

🇨🇱 Chile – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 45%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Conduct on-site and remote monitoring of clinical research studies • Verify the accuracy and completeness of collected data and adherence to study protocols • Develop and implement quality-monitoring tools, procedures, processes, templates, and checklists • Contribute to clinical trial processes, programs, policies, protocols, study design, and methodology • Manage and direct lower-level professionals or clinical trial processes and programs • Provide guidance and support to junior staff and oversee day-to-day clinical trial site activities • Ensure timely documentation and reporting of clinical trial data • Maintain detailed site-visit and monitoring records and prepare reports for regulatory submissions • Collaborate with data management, biostatistics, and regulatory affairs teams • Identify and resolve clinical trial conduct and data-integrity issues • Provide training and mentorship to junior staff

🎯 Requirements

• Bachelor's degree in a related field • Minimum of 3-5 years of experience in clinical research or a related field • In-depth knowledge of clinical trial processes and regulations • Strong analytical and problem-solving skills • Excellent communication and interpersonal skills • Ability to work independently and as part of a team • Certified Clinical Research Professional (CCRP) or equivalent certification preferred • Proficiency in clinical trial management systems and software • Strong organizational and time management skills • Attention to detail and accuracy • Ability to manage multiple projects and priorities simultaneously • Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements • Equivalent experience, skills, and/or education may be considered

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Total Self culture • Diversity, inclusion, and belonging initiatives

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume