Clinical Study Physician – Oncology

🔥 1 minute ago

🦌 Connecticut – Remote

🦌 Connecticut – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.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

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

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

Upload Resume

Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Provide medical responsibility for clinical trials throughout preparation, conduct, and reporting • Develop and review Clinical Trial Protocols and protocol updates • Contribute medical expertise to trial risk-based quality management and quality monitoring plans • Provide medical input on important protocol deviations and trial documentation • Contribute to data management documentation, eCRF design, data review plans, laboratory specifications, and data transfer agreements • Provide medical content for patient information, informed consent, monitoring manuals, communication and training plans, and statistical analysis plans • Contribute to patient narratives and Clinical Trial Report planning and review • Respond to regulators and Ethics Committees/IRBs • Provide medical input to study and site feasibility, recruitment, and retention plans • Deliver medical training to country feasibility teams, trial investigators, or sponsor staff • Conduct ongoing medical review and document findings and resolutions • Execute clinical quality monitoring, risk mitigation, and escalation of clinical quality issues • Identify inconsistencies in medical data and practical protocol execution difficulties • Respond to medical queries from investigators, CROs, and sponsor representatives • Build expert networks and contribute to site engagement • Support Endpoint Adjudication, Data Monitoring Committees, Data Safety Monitoring Boards, and Steering Committees • Review Trial Newsletters and contribute to scientific publications • Manage medical activities for one or more clinical trials • Lead cross-functional planning, execution, and analysis of clinical programs • Ensure medical assessments, decisions, and medical quality for trials, assets, and client processes • Complete required training, timesheets, expense reports, and CV updates • Maintain knowledge of and comply with Parexel processes, ICH-GCPs, and applicable requirements

🎯 Requirements

• Oncology experience • Qualified and clinically experienced physician • Physician MD, ideally with medical thesis, trained in a clinical setting • Minimum of 4 years of active clinical experience • Specialization in internal medicine or general practice preferred • Experience in the pharma industry or CRO in medical, project management, global pharmacovigilance, or another relevant medical function, ideally in Clinical Development • Understanding of relevant regulations and guidance including ICH-GCP • Experience with data visualization systems and IT systems • Proficiency with Windows and MS Office (Word, PowerPoint, Excel, Outlook) • Proficiency in written and spoken English and local language • Excellent interpersonal, active listening and influencing skills • Strong analytical, systematic, and well-structured working style • Strong presentation and training skills • Ability to work proactively and collaboratively in an international environment • Ability to use digital technologies to access information, solve problems, communicate, navigate, learn, and apply knowledge in a digital environment

🏖️ Benefits

• Equal opportunity employment • Required training curriculum • Compliance with Parexel processes, ICH-GCPs and other applicable requirements