Full-Time

Vice President/Senior Vice President

Clinical Development, Oncology

Confirmed live in the last 24 hours

Coherus BioSciences

Coherus BioSciences

201-500 employees

Develops and commercializes biosimilars for healthcare

Biotechnology
Healthcare

Compensation Overview

$275k - $375kAnnually

Senior, Expert

San Carlos, CA, USA

Category
Physicians & Surgeons
Medical, Clinical & Veterinary
Required Skills
Google Cloud Platform

You match the following Coherus BioSciences's candidate preferences

Employers are more likely to interview you if you match these preferences:

Degree
Experience
Requirements
  • M.D. required with 7+ years of experience in a clinical research role in the biopharmaceutical industry, with significant role in a leadership capacity.
  • Board certified Oncologist with oncology clinical experience and drug development experience
  • Experience directly managing clinical research staff and will have proven track record in late-stage development and regulatory filing.
  • Experience with leading early and late-stage clinical trials, regulatory filings, and product launches.
  • Ability to work effectively across functions, particularly when interfacing with clinical operations, statisticians, pharmacovigilance, and regulatory affairs.
  • Executive leadership skills to educate and influence stakeholders and to add value to strategic business planning and decision-making.
  • Exceptional interpersonal, problem-solving and written and verbal communication skills.
  • Excellent organizational and project management skills.
  • Excellent writing, organizational, and communication skills
  • Outstanding clinical and business judgment required.
  • Experience with GCP/ICH/FDA requirements, clinical trial design and strategies, commercial and publication strategy and medical information process
  • Experienced in presenting to board members, investors, potential partners, and company staff
  • Proven ability to work in a cross-functional and collaborative environment
  • Willingness and availability to travel
  • Ability to provide scientific and clinical expertise to a clinical development program and clinical strategies for a product to obtain regulatory approval
  • Demonstrated ability to establish relationships with internal colleagues and external collaborators (e.g., investigators, KOL's/CROs) and represent the company in public (e.g., scientific conferences, partners)
  • Demonstrated ability in decision-making, influencing, leadership, and affecting change by using a collaborative approach
  • Excellent knowledge of relevant FDA regulations and guidelines for conducting clinical trials
  • Must be science-and data-driven
  • Must have a results-oriented work ethic and a positive, can-do attitude
  • Must be willing and able to be 'hands on' and willing to 'roll-up sleeves' and delve into details
  • Strong business acumen
  • Highly intelligent and detail-oriented with an ability to think strategically and operationally on a wide range of issues in a solutions-oriented manner.
Responsibilities
  • Continuing the clinical development activities of our oncology products
  • Provide strategic leadership and design input for all Oncology clinical programs
  • Write / review medical aspects of core study and regulatory documents including clinical research plans, protocols, investigator brochures, clinical study reports and regulatory submissions.
  • Oversee medical monitoring support to clinical investigators and internal/external team members (e.g., address medical and eligibility questions related to clinical protocols, answer product candidate related questions)
  • Oversee safety for clinical studies (e.g., SAE reporting, ongoing review of events, integrated evaluation)
  • Review and interpret clinical trial data
  • Contribute to the development and review of scientific publications
  • Represent clinical research on internal program teams and external project teams
  • Participate in discussions with regulatory authorities as appropriate
  • Support Business Development activities as needed
Desired Qualifications
  • Prior experience working in a small/emerging company is strongly preferred
  • Experience with providing mentorship to direct reports and maintaining clear communication on performance to direct reports (preferred but not required)

Coherus BioSciences develops and sells biosimilars, which are highly similar versions of approved biologic medicines used to treat various diseases. These biosimilars are designed to be as effective and safe as the original products but are offered at a lower cost, making them more affordable for patients and healthcare systems. The company focuses on research, development, and commercialization of these products, ensuring they meet strict regulatory standards for quality and efficacy. Coherus aims to improve patient lives by expanding access to essential biologic treatments, thereby addressing the rising costs of healthcare. Their business model allows them to generate revenue through the sale of these cost-effective alternatives, giving them a competitive advantage in the biopharmaceutical market.

Company Size

201-500

Company Stage

IPO

Total Funding

$114.5M

Headquarters

Redwood City, California

Founded

2010

Simplify Jobs

Simplify's Take

What believers are saying

  • Global biosimilars market projected to grow at 24.7% CAGR from 2023 to 2030.
  • FDA guidance on biosimilar interchangeability could boost market acceptance for Coherus.
  • Collaborations with research institutes enhance development of novel therapies.

What critics are saying

  • Sandoz acquisition of Coherus' assets may lead to market share erosion.
  • 30% staff reduction could impact operational efficiency and product development.
  • Divestment of Canadian rights to Toripalimab limits revenue potential in Canada.

What makes Coherus BioSciences unique

  • Coherus focuses on cost-effective biosimilars for oncology and inflammatory diseases.
  • The company leverages advanced process science and analytical characterization in development.
  • Coherus' Udenyca wearable injector offers innovative drug delivery for pegfilgrastim.

Help us improve and share your feedback! Did you find this helpful?

Benefits

Competitive base salary

Target bonus based on performance

stock options

Medical, dental, & vision coverage

PTO

401(k) plan

FSA

Growth & Insights and Company News

Headcount

6 month growth

-1%

1 year growth

-1%

2 year growth

-2%
PE Hub
Jul 3rd, 2024
SK Capital's Apotex to acquire Canadian rights to Toripalimab

SK Capital Partners portfolio company Apotex has agreed to acquire the license to the Canadian rights to Toripalimab, an anti-PD-1 monoclonal antibody, from Coherus Biosciences.

TipRanks
Jun 5th, 2024
Coherus Biosciences Appoints Rita Karachun to Board

Coherus Biosciences appoints Rita karachun to board.

GlobeNewswire
Jun 5th, 2024
Coherus BioSciences Appoints Rita Karachun, CPA, CGMA to its Board of Directors

Coherus BioSciences appoints Rita Karachun, CPA, CGMA to its Board of Directors.

Yahoo Finance
May 8th, 2024
Coherus Announces Clinical Collaboration With The Cancer Research Institute For A Novel Combination Evaluating Loqtorzi(R) (Toripalimab-Tpzi) With Enb Therapeutics' Enb-003 For The Treatment Of Ovarian Cancer

Coherus BioSciences, Inc.REDWOOD CITY, Calif., May 08, 2024 (GLOBE NEWSWIRE) -- Coherus BioSciences, Inc. (Coherus; Nasdaq: CHRS) today announced that the Cancer Research Institute (CRI) and its Immunotherapy Platform Study in Platinum-Resistant High-Grade Serous Ovarian Cancer (IPROC) Drug Selection Committee (DSC) have selected LOQTORZI (toripalimab-tpzi), anti-PD-1 antibody, to explore in combination with ENB-003, a first-in-class small molecule inhibitor of endothelin B receptor (ETBR), for the treatment of drug-resistant cancers in the iPROC platform study. Endothelin B receptor is implicated in tumorigenesis and tumor immune suppression for several solid tumors, including melanoma, ovarian, and pancreatic cancers.“The iPROC DSC is pleased to have access to this next-generation PD-1 inhibitor and advance this combination supported by preclinical and clinical data in this study in ovarian cancer,” said John Stagg, Ph.D., Professor, Faculty of Pharmacy at the University of Montreal and Principal Investigator, Centre Hospitalier de l’Université de Montréal (CHUM) and its affiliated Cancer Institute of Montreal.Dr. Stagg continued, “The iPROC study DSC brings together a group of scientific experts within the CRI community to select promising combinations and rapidly advance them to clinical trials. Importantly, the DSC is not confined by a pipeline but looks to work with companies with drugs that have a strong data package. For this multiparty platform study to succeed, it requires science-driven, highly collaborative, and engaged companies

Fierce Pharma
Mar 13th, 2024
Coherus again axes staff, with 30% of roles on chopping block amid 'sharpened focus' on cancer drugs

After a first-in-class FDA approval in nasopharyngeal carcinoma in October, Coherus launched Loqtorzi at the beginning of 2024.