Director Clinical Development - Oncology

Who we areTogether, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.The opportunityDirector is responsible for the development, execution and management of several clinical programs worldwide across all phases of clinical research. The Director will oversee study teams and will be responsible for leading cross-functional teams in a matrix environment. The individual is expected to be able to function independently in the daily management of clinical research projects including the preparation/review of related key documents (i.e. protocols, Investigator’s Brochures, clinical study reports, summaries for regulatory submissions). The Director will provide input to the clinical development plan and will provide leadership for assigned asset strategy, working closely with other functional areas such as commercial, regulatory, pharmacovigilance, CMC, and pre-clinical development in this regard. The Director will be a key contributor to and responsible for the clinical leadership of INDs, NDAs, BLAs, and other global regulatory filings. How you’ll spend your dayThe Director will foster relationships with opinion leaders in assigned Oncology areas.Will be a core member of the Global Project TeamWill have and maintain the expertise necessary for the clinical development of the productPrepares and manages multiple Clinical Development PlansLeads or oversees the cross-functional clinical development teamSupports Global Clinical Operations in clinical trial initiation, resource planning, study implementation and successful completionMakes presentations at the Investigator Meetings and other relevant internal or external venuesResponsible for securing the required human resources to implement the Clinical Development planWorks with Clinical Supplies Group to ensure clinical drug supply plans and timely procurement with the clinical supplies groupEnsures clinical trials comply with clinical guidance, ICH, GCP, in agreement with the laws of the relevant countries and Teva Standard Operating ProceduresResolves safety or relevant clinical issues in consultation with Global Drug Safety and Pharmacovigliance, VP Clinical Research and the Head of the Global Respiratory Therapeutic Area as needed.Oversees the preparation of documents for IND/NDA and other regulatory documentsMay lead an NDA submission team independently, as neededPartners cross-functionally with departments such as Regulatory Affairs, Toxicology, CMC/Formulations, Biostatistics, Legal, Marketing, Accounting/Finance, GCO, and GCPR in the execution of Clinical Development PlansCapable of analyzing and interpreting clinical results and provide a guidance to prepare high quality reports working with Medical Writing Responsible for authoring protocol synopses and working with Medical Affairs and provides input and direction to the review and finalization of Protocols, Clinical Study Reports and other relevant clinical documentsAuthor and/or review abstracts, posters and manuscripts, present data at scientific meetings, as neededRepresent Teva at Scientific meetings, advisory boards, KOL boards and meetings with regulatory agencies, as neededThe expectation is for the person hired into this role work in a hybrid environment out of the West Chester, PA office or Parsippany, NJ office Your experience and qualificationsMD, DO or equivalent combination of education and related work experience. PhD, PharmD, DVM with strong proven track record will be consideredMinimum of 3 years experience in a pharmaceutical industry environment or related area planning/managing clinical trials, with proven ability to manage projects and/or lead project teams effectively. MD/DO without prior industry experience but with relevant knowledge and expertise, in clinical trials will be consideredExperience in the Oncology therapeutic area is strongly preferredExcellent interpersonal, verbal and written communication skills. Ability to manage multiple conflicting priorities and varied concurrent tasks, 2-4 years of managerial experience preferredStrong sense of urgency and understanding of time pressures, ability to thrive and enjoy working independently in a fast-paced, multi tasking environmentTravel:Approximately  30%,  both domestic and InternationalEnjoy a more rewarding choiceWe offer a competitive benefits package, including Medical, Dental, Vision, and Prescription coverage starting on the first day. We also offer Disability and Life Insurance, Paid Time Off, 13 paid Holidays, 6% match on the 401(k), Employee Stock Purchase Plan, and Tuition Assistance. Already Working @TEVA?If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.Teva’s Equal Employment Opportunity CommitmentTeva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.Important notice to Employment Agencies - Please Read Carefully Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities.  All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.