- Careers Integrated Resources Inc (Cambridge, MA)
- …MA Duration: 6 months + What will you do? . This position reports to the Associate Director of Clinical Outsourcing. The right candidate will possess an ... Assists teams in the identification of potential vendors and CROs for clinical trial execution . Collaboratively creates and issues Request for Proposals (RFPs),… more
- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **Job Title** : Associate Director , Clinical Quality Compliance **Location** : Cambridge, MA **About ... the role:** As the Associate Director , Clinical Quality Compliance,...Quality Compliance, you will provide quality oversight to the clinical trial delivery quality systems, promoting operational… more
- Harvard University (Cambridge, MA)
- …Sr Department Office Location:USA - MA - Boston Business Title: Associate Director of Statistical ProgrammingSub-Unit: Appointment End Date:30-Nov-2027Salary ... clinical data environment or research setting, preferably with clinical trial data + Proven skills in...the Director of Biostatistics and Programming, the Associate Director of Statistical Programming is responsible… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Programming in Cambridge, MA, where you will oversee and ... & Quantitative Sciences team, you will report to the Director , Programming. Takeda SQS is looking to add individuals...**contribute:** + Oversee and direct the work of the Clinical trial disclosure programming team (within the… more
- AbbVie (Cambridge, MA)
- …etc.) at the regional/local level. + Participation in design and execution of clinical trial safety, product safety and risk management plans. Responsible for ... substantial understanding of relevant therapeutic area required. + Knowledge of clinical trial methodology, regulatory requirements governing clinical … more
- AbbVie (Boston, MA)
- …Completion of a subspecialty fellowship is desirable. + At least 2 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent. + ... to support a global scientific and business strategy. + Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical… more
- Regeneron Pharmaceuticals (Boston, MA)
- …and/or pharmacologic) studies as per clinical strategy; Reviews, edits and finalizes clinical trial plans + Responsible for the relevance and accuracy of ... System, Neuromuscular and Muscular Diseases. **As a Senior Medical Director , a typical day may include the following:** +...academic clinical trials (10 years post fellowship clinical and research experience, associate or full… more
- Merck (Boston, MA)
- …the **Quantitative Pharmacology and Pharmacometrics -** **Immune/Oncology** team in the role of Associate Director . The team is part of the Global Clinical ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the Group will work closely with teams of… more
- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **Job Title** : Associate Director , CPMQ Strategy and Innovation **Location** : Cambridge, MA **About ... CPMQ Leadership Team, driving new opportunities in quality oversight and compliance in clinical trial delivery, providing input into R&D clinical trial … more
- Takeda Pharmaceuticals (Cambridge, MA)
- …true to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Global Publications, mature brands, is a key strategic partner ... implements the strategic global publication planning for the assigned programs. The Associate Director , Global Publications works in close collaboration with key… more
- AbbVie (Cambridge, MA)
- …substantial understanding of relevant therapeutic area required. + Knowledge of clinical trial methodology, regulatory requirements governing clinical ... level will be determined by the qualifications listed below. Purpose The Associate Scientific Director provides medical and scientific strategic and operational… more
- Pfizer (Cambridge, MA)
- …communication of statistical analyses, data presentations, and scientific reports, including clinical trial results, exploratory and meta-analysis results **,** ... biostatistics, or related field. + A minimum of 4 years' experience in the clinical trial setting (preferably in oncology of Pharma). + Relevant clinical … more
- Bristol Myers Squibb (Cambridge, MA)
- …**Summary/Scope** Reporting to Senior Scientific Director Translational Medicine (TM), the TM Associate Director will be part of the late stage TM group. The ... stage drug development and activities required for and related to clinical trial initiation, maintenance and completion + Strong verbal and written communication… more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** ** Associate Director , Nonclinical Regulatory Writing and Submission Support,** **_Oncology ... you will be a vital contributor to our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory Writing and Systems (NRWS) Department… more
- Takeda Pharmaceuticals (Boston, MA)
- …order to bring life-changing therapies to patients worldwide. Join Takeda as a Associate Director , Global Patient Safety Signal Management and Innovation in ... regulations, CIOMS and ICH guidelines. + In depth knowledge of clinical trial methodology, pharmacovigilance regulations, signal detection and risk/benefit… more
- AbbVie (Cambridge, MA)
- …Experience in Parkinson's and/or Movement Disorders is preferred. + Knowledge of clinical trial methodology, regulatory requirements governing clinical ... week onsite) in Cambridge, MA preferred. Will consider remote candidates. The Associate Scientific Director provides medical and scientific strategic and… more
- Bristol Myers Squibb (Cambridge, MA)
- …stage drug development + Experience in activities required for and related to clinical trial initiation, maintenance and completion + Experience in interacting ... Join us and make a difference. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine, the TM Sr. Principal Scientist will be part of… more
- Dana-Farber Cancer Institute (Boston, MA)
- …of advanced technology platforms that support our basic research labs, clinical trial informatics, research administration, and scientific computing. RIO ... visionary leader to join our team as the Senior Director of Product and Technology, serving our esteemed research...(CDAO). RIO is also an integral component of the Clinical Research Support Unit for the Dana-Farber/Harvard Cancer Center… more
- Robert Half Finance & Accounting (Cambridge, MA)
- …pharma R& D in Cambridge, is seeking a strong (very hands-on) Sr Manager / Associate Director level to take ownership of the R& D accounting, CT accruals, ... Pharma industry experience. + Significant experience accounting for R& D accruals, clinical trial contracts review, models, forecasting, etc + CPA MBA a plus,… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …at an academic, research, or hospital setting (such as grants management, clinical trial management, or research administration). + Background in science ... from a New England state (ME, VT, NH, MA, CT, RI).** The Assistant Director , Research Compliance will work under the oversight of Dana-Farber Cancer Institute's VP… more
