Clinical Research Manager

🔥 0 minutes ago

🌐 Belgium, Netherlands, +1 more countries – Remote

🇧🇪 Belgium – Remote 🇳🇱 Netherlands – Remote 🇩🇰 Denmark – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 11%

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.Why this score:

• Just posted.
• Jobs at this company usually fill in 42 days.
• No salary listed.

Apply Now

Find Similar Remote Jobs

BeOne Medicines

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 2010

🧬 Biotechnology

🏥 Healthcare

💊 Pharmaceuticals

Biotechnology • Healthcare • Pharmaceuticals

BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting the development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.

📋 Description

• Act as line manager for clinical research associates and trial monitoring staff • Plan, assign and direct work; assess performance and guide direct-report professional development • Participate in hiring selection and allocate resources to clinical research projects • Assign staff to clinical studies based on experience and training • Ensure clinical trial protocols comply with ICH/GCP, local regulations and applicable SOPs • Collaborate with the Regional Clinical Operations Manager to maintain study timelines and quality standards • Support study start-up and provide country-specific expertise • Onboard and train new employees and oversee training plans • Manage the quality of assigned staff’s clinical work through regular review and evaluation • Review study start-up documents, drug labels, ICFs and other applicable documents • Develop and review site-specific recruitment materials and tools • Coordinate IRB/EC submissions, TMF completeness, site activation and enrolment goals, and inspection readiness • Contribute to feasibility, site identification, selection and evaluation • Perform accompanied CRA visits and assess performance • Review visit reports, follow up on issue resolution and escalate significant risks • Monitor workload and quality metrics through regular review and reporting • Identify site issues, propose CAPAs and address gaps • Contribute to Clinical Operations strategy and performance improvement • Mentor and manage junior staff and Clinical Research Associates • Conduct mid-year and year-end performance appraisals for direct reports

🎯 Requirements

• Bachelor’s degree (or equivalent) or higher in a scientific, medical or healthcare discipline • Minimum 5+ years progressive experience in clinical operations within the biotech/pharmaceutical sector • Prior clinical trial experience, including management/leadership experience • Oncology experience highly recommended • Preferably at least 2 years of line management in the pharmaceutical or CRO industry • Ability to work independently and handle multiple priorities in a fast-paced environment • Excellent interpersonal skills and strong organizational skills • Fluent in English and the country language, in writing and speaking • Efficient in Microsoft Word, Excel, MS Project, MS PowerPoint and Outlook • Willingness to travel up to 30–40%

🏖️ Benefits

• Equal opportunity employer • Travel up to 30–40% (role-related travel allowance/expectation)

📊 Check your resume score for this job

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

Upload Resume