Careers

DAVA Oncology is a growing, entrepreneurial company with a wealth of career opportunity.  We aim to provide a work environment that fosters the development of ambitious new graduates, as well as seasoned Oncology professionals who are looking to have a more hands-on approach to expediting drug development.  DAVA recognizes that each employee brings their own unique skill-set, resulting in dynamic teams and the success of our work. Our camaraderie, strong work ethic, and positive work environment lend to quality results, as we continue to make our mark in the Oncology drug development world.   

If you feel you are suitable candidate for one of our openings and would like to join our dedicated team of employees, we encourage you to apply.

Clinical Trial Specialist/ Clinical Trial Analyst

About DAVA Oncology:

DAVA Oncology is a clinical and strategic consulting company devoted to accelerating cancer drug development.  Our company was founded in 2007 by professionals with several years of success in clinical oncology and the pharmaceutical and biotechnology industries.  Our services include Clinical Development Planning, Strategic Intelligence, and Accelerating Clinical Trials and our clients range from top pharmaceutical companies to emerging biotechnology start-ups.

OVERALL RESPONSIBILITIES:

The CTSA will support the Accelerating Clinical Trials (ACT) team by providing accrual solutions to investigators and research staff of oncology clinical trials.  This position requires regular interaction with study staff including phone conversations, accrual visits, and e-mail correspondence.  The CTSA facilitates regular interaction between DAVA Oncology’s medical oncologist team and investigative sites. The CTSA also assists in the development of tumor and trial specific educational materials for distribution to research staff. CTSAs report interactions with investigative sites and their impact on clinical trial acceleration. 

 POSITION DUTIES & RESPONSIBILITIES:

  • Regularly developing reports in PowerPoint and analyzing clinical trial data in Excel
  • Conducting research on cancer care providers and research centers
  • Preparing information for investigator or research staff calls and accrual visits
  • Engaging research staff on specific research protocols and accrual tools
  • Contributing to weekly, monthly and quarterly reports
  • Performing quantitative and qualitative data analysis on clinical trial performance
  • Scheduling and coordinating investigator workshops and teleconferences
  • Perform other tasks and duties as assigned

EDUCATIONAL & PROFESSIONAL REQUIREMENTS:

  • Bachelor’s degree with coursework in biology, health care, or management. Excellent academic record (3.5/4.0 GPA and above) Preferred: BSN or Master’s degree in biology, health care, management, pharmacy, or nurse education
  • Entrepreneurial spirit with goal driven attitude
  • Strong communication skills as demonstrated through professional and academic experiences
  • Strong quantitative and qualitative analytical ability as demonstrated through professional and academic experiences
  • Ability to work in a team environment
  • Strong computer skills, including proficiency in Microsoft Outlook, Word and PowerPoint

REQURED SKILLS:

  • Proofreading proficiency is essential
  • Keen attention to detail and commitment to high quality
  • Highly organized with ability to prioritize and work efficiently to meet tight deadlines
  • Strong communication skills (verbal and written)
  • Good critical thinking skills and proactive problem solving
  • Able to work independently yet enjoys being part of a team

If you are excited by the opportunity to improve patient care and accelerate the drug development process, please submit a resume and cover letter to Human Resources, jobs@davaonc.com or fax to (214)-889-7070 or apply online. No phone calls please.

Apply Now

Medical Director for Accrual Enhancement Support

About DAVA Oncology:

DAVA Oncology is a clinical and strategic consulting company devoted to accelerating cancer drug development.  Our company was founded in 2007 by professionals with several years of success in clinical oncology and the pharmaceutical and biotechnology industries.  Our services include Clinical Development Planning, Strategic Intelligence, and Accelerating Clinical Trials and our clients range from top pharmaceutical companies to emerging biotechnology start-ups.

OVERALL RESPONSIBILITIES:

DAVA Oncology is seeking a medical oncologist who is interested in pursuing oncology drug development in an entrepreneurial setting.  DAVA Oncology is looking for oncologists with experience in the design and conduct of phase I-III clinical trials. Medical and operational leadership with both internal personnel and external clients is critical.  A licensed ABIM board-certified/eligible MD/DO with experience in drug development and clinical trial execution is required. 

POSITION DUTIES & RESPONSIBILITIES:

  • Familiarity with clinical trial enrollment challenges and implementation of solutions to overcome accrual barriers is preferred
  • The applicant will remain current with clinical medicine and drug development information relevant to oncology in order to navigate and lead the company’s interests from a medical and business perspective
  • Assist in the development of corporate strategy and the execution of tactical plans to rapidly grow the company in the future
  • Perform other tasks and duties as assigned

EDUCATIONAL & PROFESSIONAL REQUIREMENTS:

  • Licensed and BC/BE MD/DO with a minimum of 5 years of clinical experience
  • Medical or Surgical Oncologist experience is preferred
  • Clinical research and trial experience is required
  • Dynamic presentation, moderation and facilitation skills are necessary
  • 25-50% travel is required

REQURED SKILLS:

  • Strong interpersonal leadership
  • Keen attention to detail and commitment to high quality
  • Highly organized with ability to prioritize and work efficiently to meet tight deadlines
  • Strong communication skills (verbal and written)
  • Entrepreneurial spirit and the internal drive for results is a must

If you are excited by the opportunity to improve patient care and accelerate the drug development process, please submit a resume and cover letter to Human Resources, jobs@davaonc.com or fax to (214)-889-7070 or apply online. No phone calls please.

Apply Now

Manager/Director for Scientific Affairs

About DAVA Oncology:

DAVA Oncology is a clinical and strategic consulting company devoted to accelerating cancer drug development.  Our company was founded in 2007 by professionals with several years of success in clinical oncology and the pharmaceutical and biotechnology industries.  Our services include Clinical Development Planning, Strategic Intelligence, and Accelerating Clinical Trials and our clients range from top pharmaceutical companies to emerging biotechnology start-ups.

OVERALL RESPONSIBILITIES:

DAVA Oncology has an opening for a dynamic Associate, Scientific Director who is able to demonstrate high level strategic and scientific expertise and guidance across multiple accounts and therapeutic areas (solid & liquid tumor). Specifically, the candidate will need clinical development, new product planning and commercial development knowledge. The position is an exciting opportunity to work in multi-faceted role, providing leadership to the Scientific Team, interacting with clients and assisting in Business Development.

POSITION DUTIES & RESPONSIBILITIES:

Client/internal Support:
  • Oversee the development of editorial content and direct the Science Team throughout the research, writing, editing and proofing of products, as well as the coordination with the design and production teams to produce a range of printed and computer-based materials to meet the needs of clients
  • Essential responsibilities will include department management and supervision, research and information management, general writing and business development assistance
  • The ability to combine in-depth scientific understanding of the product/therapy area with commercial/market awareness to provide high level scientific, strategic and marketing insights for clients. Specifically, for the following clinical, new product and commercial products
  • Qualitative Insight &Advisory Feedback, Clinical & Competitive Landscape Analyses, Clinical Development Strategies, Standard of Care Reference Guides, Strategic Life Cycle Management and Congress Coverage
  • Develop successful relationships with pharmaceutical clients, scientific staff and internal teams
  • Present authoritatively and with credibility to client commercial, medical and scientific staff
Delivery:
  • Ensure highest standards of quality control and client service, while meeting tight timelines
  • Support and maintain team focus with colleagues across the Scientific Team
  • High-level mentoring of other writers and support staff in team, to include involvement with identification and delivery of scientific training needs across account team
Business Development:
  • Utilize therapy area expertise and commercial understanding to support proposal development and build understanding across account team
  • Responsible for driving organic growth by establishing positive long-term relationships with clients, contributing to business development activities and recruiting a successful team

EDUCATIONAL & PROFESSIONAL REQUIREMENTS:

  • Advanced life science degree (MS, PharmD or preferably PhD)
  • Excellent medical writing skills and exposure to a wide range of communication activities
  • Strong communication skills as demonstrated through professional and academic experiences
  • Strong therapeutic area, product and market knowledge to serve as client lead
  • Publications experience with Oncology (solid & liquid tumor)
  • Strong computer skills, including proficiency in Microsoft Outlook, Word and PowerPoint
  • Advanced Microsoft Office, specifically Power Point skills

REQURED SKILLS:

  • Keen attention to detail and commitment to high quality
  • Highly organized with ability to prioritize and work efficiently to meet tight deadlines
  • Strong communication skills (verbal and written)
  • Good critical thinking skills and proactive problem solving
  • Creativity and an eye for design are a plus

If you are excited by the opportunity to improve patient care and accelerate the drug development process, please submit a resume and cover letter to Human Resources, jobs@davaonc.com or fax to (214)-889-7070 or apply online. No phone calls please.

Apply Now

Clinical Trial Liaison

About DAVA Oncology:

DAVA Oncology is a clinical and strategic consulting company devoted to accelerating cancer drug development.  Our company was founded in 2007 by professionals with several years of success in clinical oncology and the pharmaceutical and biotechnology industries.  Our services include Clinical Development Planning, Strategic Intelligence, and Accelerating Clinical Trials and our clients range from top pharmaceutical companies to emerging biotechnology start-ups.

OVERALL RESPONSIBILITIES:

The Clinical Trial Liaison is actively involved in Marketing by one-to-one contacts and professional education. The position requires the ability to work independently and to prioritize responsibilities. An outgoing personality, assertiveness, the ability to deal with various levels of clients, and effective verbal and written communication skills are also required.

 POSITION DUTIES & RESPONSIBILITIES:

  • Responsible for developing and executing study communications plans for multiple cancer clinical trials
  • Local travel to hospitals, academic centers and community oncology practices is required
  • Establish new relationships with clinical researchers
  • Provide a mentoring and information service for clinical research staff and MDs
  • Interact with Pharmaceutical/Biotech Industry Sponsors to provide insight and updates on trial progress
  • Assist in identifying trial specific issues and opportunities for developing solutions
  • Help increase study accrual will be paramount
  • Perform other tasks and duties as assigned

EDUCATIONAL & PROFESSIONAL REQUIREMENTS:

  • A minimum of MS degree is required, PhD is preferred
  • Clinical background
  • Registered Nurse (RN) preferred
  • Sales and/or marketing is preferred and computer experience is required
  • Previous experience in collaborating with and/or supporting Marketing, Clinical Research & Development and Medical Affairs business groups is preferred

REQURED SKILLS:

  • Leadership skills, excellent communication skills
  • Problem solving at a strategic level, working with others to reach a resolution
  • Ability to discuss strategic and sensitive issues
  • Confident approach balanced with strong listening skills
  • Ability to develop a deep understanding of medical device research and development, manufacturing processes, marketing, clinical trials, regulatory affairs and relevant legal requirements

If you are excited by the opportunity to improve patient care and accelerate the drug development process, please submit a resume and cover letter to Human Resources, jobs@davaonc.com or fax to (214)-889-7070 or apply online. No phone calls please.

Apply Now

Clinical Pathologist

About DAVA Oncology:

DAVA Oncology is a clinical and strategic consulting company devoted to accelerating cancer drug development.  Our company was founded in 2007 by professionals with several years of success in clinical oncology and the pharmaceutical and biotechnology industries.  Our services include Clinical Development Planning, Strategic Intelligence, and Accelerating Clinical Trials and our clients range from top pharmaceutical companies to emerging biotechnology start-ups.

OVERALL RESPONSIBILITIES:

DAVA Oncology is seeking an experienced clinical pathologist to work with a team of medical oncologists in pursuing oncology drug development in an entrepreneurial setting. DAVA works on accelerating the conduct of oncology clinical trials from phase I-III. Due to the unique challenges associated with biomarker use in current clinical trials, DAVA is recruiting a clinical pathologist to liaise with pathologists, clinical trial investigators and sponsors to help overcome barriers to accrual. 

POSITION DUTIES & RESPONSIBILITIES:

  • Familiarity with clinical trial enrollment challenges and implementation of solutions to overcome accrual barriers is preferred
  • The applicant will remain current with clinical pathology relevant to oncology in order to navigate and lead the company’s interests from a medical and business perspective
  • Assist in the development of corporate strategy and the execution of tactical plans to rapidly grow the company in the future
  • Perform other tasks and duties as assigned

EDUCATIONAL & PROFESSIONAL REQUIREMENTS:

  • Licensed and board certified MD/DO with a minimum of 5 years of clinical pathology experience
  • Clinical research and trial experience is preferred
  • Dynamic presentation skills are necessary
  • 10-20% travel may be required

REQURED SKILLS:

  • Strong interpersonal leadership
  • Keen attention to detail and commitment to high quality
  • Highly organized with ability to prioritize and work efficiently to meet tight deadlines
  • Strong communication skills (verbal and written)
  • Entrepreneurial spirit and the internal drive for results is a must

If you are excited by the opportunity to improve patient care and accelerate the drug development process, please submit a resume and cover letter to Human Resources, jobs@davaonc.com or fax to (214)-889-7070 or apply online. No phone calls please.

Apply Now

Patient Recruitment Specialist

About DAVA Oncology:

DAVA Oncology is a clinical and strategic consulting company devoted to accelerating cancer drug development.  Our company was founded in 2007 by professionals with several years of success in clinical oncology and the pharmaceutical and biotechnology industries.  Our services include Clinical Development Planning, Strategic Intelligence, and Accelerating Clinical Trials and our clients range from top pharmaceutical companies to emerging biotechnology start-ups.

OVERALL RESPONSIBILITIES:

The Patient Recruitment Specialist is actively involved in providing services to patients by assisting with matching them to appropriate clinical trial options. In addition, the Patient Recruitment Specialist is responsible for the project management of patient recruitment efforts, to include team training and timelines, as well as business development. The position requires the ability to think creatively and prioritize responsibilities. An outgoing personality, assertiveness, the ability to deal with various levels of patient and client contacts, as well as effective verbal and written communication skills are also required

 POSITION DUTIES & RESPONSIBILITIES:

  • Responsible for managing project timelines related to marketing campaigns, patient and investigator material development and call center initiatives
  • Creation and teaching of a comprehensive training curriculum both for new hire orientation and ongoing training needs related to trial education and patient recruitment processes
  • Assist with the development of a DAVA clinical trial portal from concept to implementation. This will include customized data feeds, online prescreening capability for clinical trials and access to call center assistance
  • Oversee the development of patient recruitment materials and physician directed marketing and educational tools
  • Provide mentoring, information services, and other trial support as required by the staff and patients
  • Identification of potential clinical trials DAVA could support, as well as marketing of the patient portal to Pharmaceutical/Biotech Industry sponsors
  • Helping to increase patient trial awareness and accrual will be paramount
  • Perform other tasks and duties as assigned

EDUCATIONAL & PROFESSIONAL REQUIREMENTS:

  • Bachelor’s degree required, advanced degree a plus
  • Prior experience in patient recruitment, preferably in a leadership role, for a pharmaceutical company, CRO or patient recruitment firm
  • Sales and/or marketing experience is a plus
  • 25% travel is required

REQURED SKILLS:

  • Leadership skills, excellent communication skills
  • Problem solving at a strategic level, working with others to reach a resolution
  • Ability to develop a deep understanding of the oncology space, clinical research and development, marketing, clinical trials, regulatory affairs and relevant legal requirements

If you are excited by the opportunity to improve patient care and accelerate the drug development process, please submit a resume and cover letter to Human Resources, jobs@davaonc.com or fax to (214)-889-7070 or apply online. No phone calls please.

Apply Now

Project Manager

About DAVA Oncology:

DAVA Oncology is a clinical and strategic consulting company devoted to accelerating cancer drug development.  Our company was founded in 2007 by professionals with several years of success in clinical oncology and the pharmaceutical and biotechnology industries.  Our services include Clinical Development Planning, Strategic Intelligence, and Accelerating Clinical Trials and our clients range from top pharmaceutical companies to emerging biotechnology start-ups.

OVERALL RESPONSIBILITIES:

The Project Manager (PM) is the primary interface between the sponsor and DAVA Oncology. Plans, directs, and coordinates activities of the ACT project to ensure that enrollment goals and objectives of the project are accomplished within time frame. Oversees and coordinates the operational aspects of the project and serves as a liaison between Senior Management, Medical Oncologists and Clinical Trial Specialists/Analysts. Assesses project issues and develops resolutions to meet productivity, quality, and client-satisfaction goals and objectives.

POSITION DUTIES & RESPONSIBILITIES:

  • Assist Business Development Team with proposal writing including enrollment forecast, contractual language and accrual enhancement strategies
  • Assign and manage Clinical Trial Specialists/Analysts
  • Ensure that Clinical Trial Specialists/Analysts allocated to assigned projects adhere to professional standards and appropriate SOPs established for ACT projects
  • Assign day to day tasks to Clinical Trial Specialists/Analysts
  • Monitor and provide feedback to Clinical Trial Specialists/Analysts regarding their completed tasks
  • Set weekly, monthly and quarterly goals for Clinical Trial Specialists/Analysts
  • Coordinate and discuss with DAVA Medical Oncologists site recommendation priorities & final recommendation
  • Coordinate and discuss with DAVA Medical Oncologists accrual enhancement strategies
  • Coordinate and discuss with DAVA Medical Oncologists MD to MD call prioritization
  • Bridge communication gaps between DAVA Medical Oncologists and Clinical Trial Specialists/Analysts
  • Manage site visits for various ACT projects and oversee completion of site visit reports
  • Initiate improvements to enhance the efficiency and the quality of the work performed
  • Prepare and present weekly, monthly and quarterly presentations to client
  • Prepare and present trial progress reports and notes to DAVA Senior Management
  • Establish excellent working relationships with client, project teams and Senior Management to ensure client satisfaction and operational excellence
  • Ensure proper training and create training materials if needed 

EDUCATIONAL & PROFESSIONAL REQUIREMENTS:

  • Bachelor’s degree, GPA 3.5 or higher
  • 2 to 3 years’ experience, technical or medical-related field preferred
  • Basic Microsoft Office (Word, Power Point and Excel) user skills are essential and intermediate to advanced skills are highly preferred.

REQURED SKILLS:

  • Keen attention to detail and commitment to high quality
  • Highly organized with ability to prioritize and work efficiently to meet tight deadlines
  • Strong communication skills (verbal and written)

If you are excited by the opportunity to improve patient care and accelerate the drug development process, please submit a resume and cover letter to Human Resources, jobs@davaonc.com or fax to (214)-889-7070 or apply online. No phone calls please.

Apply Now

Research Associate

About DAVA Oncology:

DAVA Oncology is a clinical and strategic consulting company devoted to accelerating cancer drug development.  Our company was founded in 2007 by professionals with several years of success in clinical oncology and the pharmaceutical and biotechnology industries.  Our services include Clinical Development Planning, Strategic Intelligence, and Accelerating Clinical Trials and our clients range from top pharmaceutical companies to emerging biotechnology start-ups.

OVERALL RESPONSIBILITIES:

The Oncology Research Analyst candidate will be expected to develop a comprehensive scientific and clinical knowledge base for assigned therapeutic area (solid & liquid tumor), as well as a deep understanding of the drug development process.? The candidate would be involved in the identification of drugs in development, evaluation of clinical opportunities, and monitoring the initiation and progress of clinical research trials.?

POSITION DUTIES & RESPONSIBILITIES:

  • Research, writing, editing and proofing to produce a range of printed and computer-based materials to meet the needs of clients
  • Strong scientific understanding of the product/therapy (solid & liquid tumor) areas to provide scientific and strategic guidance for clients
  • Secondary Research: Acquire information from internet sources, journals, public databases, etc.
  • Attendance at major cancer conferences world-wide to obtain scientific updates
  • Work collectively with the Associate, Scientific Director, pharmaceutical clients, scientific staff and internal teams to clearly define project scope, set expectations and finalize deliverables

EDUCATIONAL & PROFESSIONAL REQUIREMENTS:

  • Master’s or PhD in Biomedical Sciences (molecular biology, biochemistry, signal transduction or any related field that will facilitate understanding of clinical oncology data)
  • 2 years post graduate experience would be a plus as would any familiarity with drug development.?
  • Strong computer skills, including proficiency in Microsoft Outlook, Word and PowerPoint

REQURED SKILLS:

  • Outstanding communication skills
  • A scrupulous attention to detail are essential for the delivery of timely, high-quality client deliverables and other written communications
  • Inquisitive mind and a team-oriented attitude
  • Keen attention to detail and commitment to high quality
  • Highly organized with ability to prioritize and work efficiently to meet tight deadlines
  • Able to work independently yet enjoys being part of a team

If you are excited by the opportunity to improve patient care and accelerate the drug development process, please submit a resume and cover letter to Human Resources, jobs@davaonc.com or fax to (214)-889-7070 or apply online. No phone calls please.

Apply Now

Oncology Research Nurse Specialist

About DAVA Oncology:

DAVA Oncology is a clinical and strategic consulting company devoted to accelerating cancer drug development.  Our company was founded in 2007 by professionals with several years of success in clinical oncology and the pharmaceutical and biotechnology industries.  Our services include Clinical Development Planning, Strategic Intelligence, and Accelerating Clinical Trials and our clients range from top pharmaceutical companies to emerging biotechnology start-ups.

OVERALL RESPONSIBILITIES:

DAVA Oncology is looking for oncology research nurses to help accelerate accrual to cancer clinical trials. The candidate must have clinical experience in the care of oncology patients and significant clinical trial experience.  The candidate will be someone who has served in the role of study coordinator for oncology research trials or who has been a clinical research associate (CRA) for oncology trials with either a contract research organization or pharmaceutical company. 

 POSITION DUTIES & RESPONSIBILITIES:

  • Telephone contact with individual sites
  • Teleconferences with research coordinators to discuss particular issues with clinical trials
  • Travel to various oncology practices 
  • Interactions with practicing investigators, study coordinators and other site staff

EDUCATIONAL & PROFESSIONAL REQUIREMENTS:

  • Graduate from an accredited program for professional nursing education, advanced degree preferred
  • Clinical oncology nursing experience
  • Experience as a study coordinator or clinical research associate (CRA) for oncology trials

REQURED SKILLS:

  • Communicate effectively, both verbally and in writing, is required.
  • Keen attention to detail and commitment to high quality
  • Highly organized with ability to prioritize and work efficiently to meet tight deadlines
  • Able to work independently yet enjoys being part of a team

If you are excited by the opportunity to improve patient care and accelerate the drug development process, please submit a resume and cover letter to Human Resources, jobs@davaonc.com or fax to (214)-889-7070 or apply online. No phone calls please.

Apply Now

 

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