Senior Clinical Research Scientist (Biotechnology, Remote)

Job summary

This role is focused on implementing global development strategies by leading or co-leading clinical trials in various therapeutic areas. The position involves oversight of clinical development processes and collaboration with cross-functional teams to ensure timely and high-quality deliverables.

Responsibilities

• Lead or co-lead clinical trials for compounds in different stages of development, ensuring adherence to global strategies.
• Develop program strategies for assigned trials and contribute to clinical development plans.
• Collaborate with Medical Directors to create clinical and regulatory documents, including protocols and safety updates.
• Assist in the development of electronic case report forms and provide scientific support for data management tasks.
• Conduct ongoing data reviews and summarize efficacy and safety data for analysis.
• Engage in country/site selection and feasibility assessments, and interact with key opinion leaders.
• Prepare and coordinate internal and external committee meetings, including presentation materials.
• Liaise with project teams and CROs, contributing to study plans and publications.
• Mentor junior Clinical Research Scientists as needed.

Qualifications

• PhD, Pharm D, MS, or equivalent in medical, biological, pharmaceutical science, or related fields.
• At least 6 years of clinical research experience, with a minimum of 3 years in drug development, preferably in oncology.
• Experience in a project-oriented, matrixed team environment.
• Strong knowledge of Good Clinical Practice (GCP) and clinical research methodologies.
• Proven ability to work under pressure and meet tight deadlines.
• Excellent communication skills, both written and verbal.

Skills

• Collaborative team player with experience working with diverse stakeholders.
• Strong problem-solving abilities and innovative thinking.
• Passionate about improving patient outcomes and committed to excellence in work.

Education

• Advanced degree (PhD, Pharm D, MS) in relevant scientific disciplines preferred.

Tools

• Familiarity with clinical trial management systems and data management tools.