VP, Medical & Clinical Affairs

Company: Jobot
Location: Salem
Posted on: May 10, 2022

Job Description:

VP, Medical & Clinical (oncology) // Small Biotech // Well funded, Renowned Leadership

This Jobot Job is hosted by Rick Fleenor

Are you a fit? Easy Apply now by clicking the "Apply" button and sending us your resume.

Salary $275,000 - $375,000 per year

A Bit About Us

Our approach draws on novel insights into targeting signaling pathways that drive the activation, migration and invasion of abnormal cells into healthy tissues. Focused on life-threatening diseases, including cancer and fibrosis.

Why join us?

Seasoned and renowned leadership
Privately held
Strong compensation base, bonus, and equity options
Entrepreneurial culture

Job Details

Summary
The VP, Medical & Clinical provides day-to-day oversight and management of clinical trials.
Manages relationships with site investigators, clinical site personnel, medical personnel at CROs and/or medical consultants, and key opinion leaders.
Scope of work includes the development of trial concepts; review of protocols, amendments, informed consents, and case report forms; work with relevant functions in the project team to respond to relevant regulatory questions; evaluation of trial eligibility; monitoring of data entry including safety data; data analysis; CSR authoring; review of investigational brochure updates; authoring and review of briefing documents.
Works closely with the project team to assure current medical standards are embedded in clinical studies. Domestic and international travel will be required.
Specifically accountable for outreach to clinical trials sites, ensuring sites are educated on our clinical trials and ensuring the appropriate patients are enrolled in our studies, both of which should result in ensuring clinical trials enroll on time.
Develop strong relationships with internal clinical trial managers, CRO clinical trial managers, GOG/ENGOT personnel, as well as clinical sites.
Also responsible for keeping the Our team informed on competing clinical trials.

Required Skills & Abilities
Ability to write reports, protocols, investigational brochures, regulatory responses and briefing documents.
Ability to effectively present information and respond to questions from groups of personnel.
Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.
Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
Demonstrated working knowledge of Microsoft Word, Excel and PowerPoint.
Working knowledge of common EDC applications
Strong organizational skills.
Detail oriented and accurate.
Ability to multi-task and prioritize work assignments with little supervision.
Ability to work collectively with team members.

Qualifications
MD or MD/PhD
A minimum of 5 years' experience as a clinical director, with increasing levels of responsibility, in the Pharmaceutical, Biotechnology, Medical Device and/or CRO industry
Therapeutic experience in oncology (preferred)
Experience in all trial phases (Phase I-III), First-In-Man trials (preferred)

Interested in hearing more? Easy Apply now by clicking the "Apply" button.

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