Department: Medical Research
Job Title: Medical Director – Oncology
Description:
We are seeking an independent, highly motivated individual who desires an opportunity to excel in a team environment and make key contributions as a member of the medical research department in a fast-paced biotechnology company focusing on oncology.
Responsibilities
Responsibilities will include working with the medical team to plan and conduct clinical trials of novel anti-tumor agents, which involves meeting with prospective investigators, providing medical expertise to protocol design, overseeing trial start-up activities, evaluating trial progress, reviewing trial data and maintaining contact with the investigators and trial sites. In addition, responsibilities will include to: (1) serve as a key member of program development teams by providing input to program plans, (2) present trial results both inside and outside the company, (3) provide appropriate medical monitoring of key efficacy/safety parameters, (4) assist and/or oversee the preparation of interim and final clinical study reports as well as investigator brochures, (5) prepare material for regulatory agencies and (6) effectively collaborate with colleagues in related project team departments such as Regulatory, Quality Assurance, Manufacturing, Bioanalytical and Discovery. This position has responsibility for and oversight of the activities involved in the successful implementation of medical projects.
Job Description
As a key member of the medical research team, you will participate in the gamut of activities involved in the preparation for and implementation of clinical trials as well as provide medical input to cross-functional teams. You will plan, implement, evaluate and interpret clinical research on investigational products. In addition, you will be expected to provide medical expertise and clinical judgment to all aspects of a drug development program.
You will have the exciting opportunity to contribute substantially to the successful implementation of Phase 1 and 2 clinical trials with the lead candidate at ARIAD as well as additional programs as appropriate, and will report directly to the Chief Medical Officer.
Job Requirements:
The successful candidate must be an MD or MD/PhD with full subspecialty training in oncology/hematology, and have either a minimum of two years of biotechnology/pharmaceutical work experience after completion of training, or exceptional qualification for the position, such as relevant experience during training. An exceptional individual with a PhD, extensive expertise in oncology/hematology and greater number of years of experience may be considered. Effective oral and written communication skills are required, as are excellent interpersonal skills with demonstrated ability to work in a team environment as well as independently, and thrive in a fast-paced environment. Previous industry, pharmaceutical, or regulatory experience, or outstanding academic achievement in a related field will be considered. Travel time is approximately 20% including visits to investigative sites and attendance at major oncology meetings.
