Clinical Scientist
3 weeks ago
Position Overview
This position supports the scientific planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate your technical skills, and scientific acumen as part of a global, cross-functional team. Responsible for leading specific aspects of clinical/scientific execution of clinical protocol(s).
Responsibilities
Serve as clinical scientist on the clinical trial team
Support the medical monitoring team in review and interpretation of clinical data and medical protocol deviations
Provide data review per Data Review Guideline to ensure high-quality data of the study on an ongoing basis
Collaborate cross-functionally in the development of study protocol and related study materials (e.g., ICF documents/amendments); Partner with Clinical Operations on study deliverables
Provide study related data to support regulatory documents (e.g., investigator brochure)
Ensure CRF design supports data collection in alignment with the protocol in collaboration with Data Management/Programming
Support site initiation activities and interactions with site staff
Collaborate cross-functionally to monitor clinical data to ensure quality, completeness, and integrity of trial conduct
Support investigator meeting(s), IDMC meeting(s) and thought leader interactions
Qualifications
Degree in life sciences (such as medicine, pharmacy, biology) with at least 3-years’ experience in clinical research/development required.
Advanced degree (MD, PhD, PharmD or Master’s Degree) with at least 2-years’ experience in clinical oncology research/development preferred, but not required.
Solid knowledge of clinical research regulatory requirements (e.g., GCP and ICH).
Ability to manage multiple competing priorities with good planning, time management and prioritization skills.
Strong analytical skills with the ability to interpret clinical trial data and synthesize conclusions.
Interact with key stakeholders across department, division, and company to achieve study goals with high quality and during the agreed time.
Problem solving, prioritization, conflict resolution, and critical thinking skills.
Strong communication, technical writing, and presentation skills.
Company Overview
Bicara Therapeutics is a clinical-stage biotechnology company developing first-in-class biologics engineered to bring together the precision of targeted therapy and the power of tumor modulators. The company’s bifunctional antibodies are designed to deliver an immunomodulatory payload directly to the tumor microenvironment to ramp up immune cell activity, potentially offering long-lasting efficacy. Bicara’s lead asset, BCA101, a first-in-class EGFR / TGF-β-trap bifunctional antibody, is currently enrolling patients in a Phase 1/1b study. Bicara’s experienced team brings deep expertise across immunology, oncology, clinical development, business development and operational strategy. More information is available at www.bicara.com.
Here at Bicara, we believe in building diverse teams and cultivating a culture where all voices are included. We encourage people from all backgrounds to apply.
Bicara Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.
To apply, please email your resume/CV to careers@bicara.com. In the subject line include your name and the job title.
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