Clinical Research Physician
Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing clinical cancer research.
TRIO is looking for a Clinical Research Physician to join our Medical Monitoring Unit team. Reporting to the Medical Monitoring Unit Manager, this will be a home-based, full-time position in Spain.
Main Responsibilities:
Act as Medical Monitor, performing comprehensive medical monitoring activities.
Respond to medical inquiries from investigational sites and trial teams.
Review patient eligibility and protocol deviations.
Oversee patient safety by reviewing medical data at patient and trial levels.
Review Serious Adverse Events (SAEs), including coding, causality and expectedness assessments, and drafting company comments.
Prepares scientific slides, attends and/or presents protocol information at Investigator Meetings, Scientific Committee meetings, Safety Review Committee meetings, SIVs, etc.
Serve as the primary clinical point of contact for scientific questions from internal and external stakeholders (e.g., IRBs, sites, sponsor medical teams, trial teams).
Collaborates with the Medical Writing and Training Unit to write and/or review trial-specific medical documents (e.g., protocols, DSURs, CSRs).
Conducting medical training on selected trial-specific or non-trial-specific topics.
Qualifications:
Medical Doctor degree required
Excellent knowledge and understanding of oncology and oncology clinical trials
At least 1 year of experience in medical monitoring in oncology trials
Current knowledge of ICH GCP guidelines
Advanced proficiency in MS Office in Word, Excel, and PowerPoint
Strong teamwork abilities and communication skills
Excellent level of English is required
Spanish language knowledge will be valued
Must be legally authorized to work in the country
What TRIO Can Offer You:
Annual competitive review with opportunities for professional growth
Paid vacation days
Flexible working hours to promote work-life balance
Monthly Internet Allowance to support working from home
Remote work arrangements with a one-time home office allowance
Employee Recognition Program to reward long-term employees
Employee Referral Bonus Program
We thank all candidates for their interest; only those selected for an interview will be contacted.
Prior to applying please review TRIO's Applicant Information Notice
To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI.
To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments. We want the opportunity to get to know you and your experience.
Teamwork · Passion · Integrity · Innovation
Apply To This Job
TRIO is looking for a Clinical Research Physician to join our Medical Monitoring Unit team. Reporting to the Medical Monitoring Unit Manager, this will be a home-based, full-time position in Spain.
Main Responsibilities:
Act as Medical Monitor, performing comprehensive medical monitoring activities.
Respond to medical inquiries from investigational sites and trial teams.
Review patient eligibility and protocol deviations.
Oversee patient safety by reviewing medical data at patient and trial levels.
Review Serious Adverse Events (SAEs), including coding, causality and expectedness assessments, and drafting company comments.
Prepares scientific slides, attends and/or presents protocol information at Investigator Meetings, Scientific Committee meetings, Safety Review Committee meetings, SIVs, etc.
Serve as the primary clinical point of contact for scientific questions from internal and external stakeholders (e.g., IRBs, sites, sponsor medical teams, trial teams).
Collaborates with the Medical Writing and Training Unit to write and/or review trial-specific medical documents (e.g., protocols, DSURs, CSRs).
Conducting medical training on selected trial-specific or non-trial-specific topics.
Qualifications:
Medical Doctor degree required
Excellent knowledge and understanding of oncology and oncology clinical trials
At least 1 year of experience in medical monitoring in oncology trials
Current knowledge of ICH GCP guidelines
Advanced proficiency in MS Office in Word, Excel, and PowerPoint
Strong teamwork abilities and communication skills
Excellent level of English is required
Spanish language knowledge will be valued
Must be legally authorized to work in the country
What TRIO Can Offer You:
Annual competitive review with opportunities for professional growth
Paid vacation days
Flexible working hours to promote work-life balance
Monthly Internet Allowance to support working from home
Remote work arrangements with a one-time home office allowance
Employee Recognition Program to reward long-term employees
Employee Referral Bonus Program
We thank all candidates for their interest; only those selected for an interview will be contacted.
Prior to applying please review TRIO's Applicant Information Notice
To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI.
To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments. We want the opportunity to get to know you and your experience.
Teamwork · Passion · Integrity · Innovation
Apply To This Job