Senior Clinical Scientist

Unicon Pharma Inc; United States; On-site; USD 110,000 - 150,000; Full time

Job summary

Unicon Pharma Inc. is seeking a Clinical Science professional to support early-phase oncology trials in NSCLC, bladder cancer, and ovarian cancer.

You will help shape study design, protocols, and data review while collaborating with cross-functional teams to ensure high-quality clinical outputs. The role emphasizes pharmacovigilance, biomarker strategy support, and active contribution to trial oversight, with opportunities to leverage AI tools to optimize workflows.

Qualifications

• Bachelor's degree with 3+ years of relevant clinical experience, or an advanced degree (PharmD/PhD) with 1–3 years of relevant experience preferred.
• Experience supporting clinical trials, preferably Phase I–II oncology studies.
• Proficiency in Medidata Rave is required.

Responsibilities

• Support clinical study strategy, design, planning, and execution.
• Draft and review clinical development plans, study protocols, and informed consent forms (ICFs).
• Review clinical data, patient profiles, listings, and study outputs to support data quality.
• Collaborate with Clinical Operations, Biostatistics, Data Management, CROs, and AROs.
• Contribute to Statistical Analysis Plans (SAPs), Clinical Study Reports (CSRs), and regulatory submission documents.
• Support biomarker and PK strategy, literature reviews, and study team activities.
• Participate in CRO/ARO discussions, study meetings, and clinical trial oversight.

Skills

Clinical trial design

Data review

Project management

Communication

Education

Bachelor's degree

PharmD/PhD

Tools

Medidata Rave

AI tools (Copilot/ChatGPT/Claude)

Job description

We are seeking a Clinical Science professional to support early-phase oncology clinical trials, with a focus on Non-Small Cell Lung Cancer (NSCLC), Bladder Cancer, and Ovarian Cancer.

Key Responsibilities:

• Support clinical study strategy, design, planning, and execution.
• Draft and review clinical development plans, study protocols, and informed consent forms (ICFs).
• Review clinical data, patient profiles, listings, and study outputs to support data quality.
• Collaborate with Clinical Operations, Biostatistics, Data Management, CROs, and AROs.
• Contribute to Statistical Analysis Plans (SAPs), Clinical Study Reports (CSRs), and regulatory submission documents.
• Support biomarker and PK strategy, literature reviews, and study team activities.
• Participate in CRO/ARO discussions, study meetings, and clinical trial oversight.

Required Qualifications:

• Bachelor's degree with 3+ years of relevant clinical experience, or an advanced degree (PharmD/PhD) with 1–3 years of relevant experience preferred.
• Experience supporting clinical trials, preferably Phase I–II oncology studies.
• Knowledge of clinical study protocols, clinical data review, and study execution.
• Proficiency in Medidata Rave is required.
• Strong scientific knowledge, critical thinking, communication, and project management skills.
• Ability to work collaboratively in a fast-paced, deadline-driven environment.

Preferred:

• Experience in NSCLC, bladder cancer, or ovarian cancer.
• Familiarity with AI tools such as Microsoft Copilot, ChatGPT, or Claude.