CBCC Global Research · 10 hours ago
Senior Vice President Clinical Oncology
United States
Full-time
Remote
Director/Executive
10+ years expREV Clinical, a leading multi-national clinical contract research organization headquartered in Bakersfield, California, is seeking a Senior Vice President of Clinical Oncology. This role involves designing, leading, and delivering clinical trial programs in advanced therapeutic areas while representing the company in high-level client interactions and overseeing the clinical team.
MedicalPharmaceuticalProduct Research
Hiring Manager
Anshika Sharma
Responsibilities
Work directly with REV Clincial’s Senior Leadership Team and Board to define and execute the company’s clinical program strategies, particularly in Oncolgy and CNS, focused on biologic drugs, ADC’s and innovator small molecule platforms from Phase I-IV
Serve as medical and clinical leader in designing CBCC’s clinical trial program offerings and delivery
Define and coordinate on clinical trial design, protocol development and regulatory strategies with new and existing biopharmaceutical customers in Phase I-IV clinical trials
Provide medical oversight for clinical trials, including safety, data review, and scientific input
Ensure the highest standards in medical deliverables (protocols, safety narratives, clinical study reports)
Support regulatory strategy and contribute to key submissions (e.g., IND, CTA, NDA documents)
Act as the senior clinical advisor during pre-sales and study design, proposals, and bid defence meetings
Build trusted relationships with leading biotech/pharma sponsors, key opinion leaders (KOLs), site networks and investigators
Communicates up, down, and across the company to share progress, solutions, and future vision
Able to communicate with highly scientific client-management teams
Has listening skills that embrace cognitive diversity
Stays informed and communicates to others in a supportive manner regarding corporate activities
Directs and oversees recruitment, hiring, supervision, coaching, and evaluation of clinical team
Develops, encourages, and provides ongoing education and professional development
Builds and maintains positive relationships with management, peers, and subordinates
Qualification
Required
MD or MD/PhD with leading medical research, clinical trial and drug development experience
Minimum 10 years of experience in clinical development with direct experience with early-phase (Phase I/II) and complex trials (Oncology, CNS and rare diseases)
Recent participation and leadership in designing clinical trials and regulatory strategies in the ADC, biologics drug and innovator small molecule space
Has led advanced clinical program designs and execution, potentially as an Assistant/Associate Professor in Oncology at a top clinical teaching hospital, as a PI in an NCI designated clinical center, and has collaborated directly with leading biopharmaceutical companies in clinical trial design, regulatory strategy, execution and delivery
Proven ability to manage multiple clinical programs, navigate regulatory environments, and communicate/coordinate with clients
Entrepreneurial mindset and willingness to roll up sleeves and build from the ground up
Strong knowledge of ICH-GCP, FDA, EMA, and other global regulatory frameworks
Exceptional problem solving and analytical skills, combined with impeccable business judgment and the ability to communicate with highly scientific client-management teams
Senior-level writing skills, oral communication, and interpersonal skills
Absolute integrity as a leader and ability to be quickly seen as a role model for leadership
Ability to work effectively in a team-oriented setting; willing and open to contribute to other work groups in terms of personality and competence
Proven track record of effectively driving large scale pharma partnering initiatives; including ability to win program engagements, shape and influence customer agenda & programs
Attention to detail and ability to work simultaneously on multiple priorities
Adaptable and flexible to changing priorities
Preferred
Prior experience working in clinical trial design and execution with a biotech, CRO or early-stage clinical environment
Company
CBCC Global Research
CBCC Global Research is a full service clinical contract research organization serving a wide spectrum of clinical research services including Phase II-IV clinical trials services, medical writing, Data Management, regulatory services, post marketing registry trials to the Bio-Pharmaceutical, Medical device, and Diagnostics companies.
51-200 employees
H1B Sponsorship
CBCC Global Research has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2024 (1)
2023 (1)
2022 (1)
2021 (1)
Funding
Current Stage
Growth StageLeadership Team
Manoj Vyas
Chief Executive Officer
Recent News
Los Angeles Business Journal
2025-04-15
NeOnc Technologies Holdings, Inc.
2025-03-27
Company data provided by crunchbase