Associate Director, PV Sciences, Global Medical Safety Oncology - Boston, MA

Supports the Global Safety Lead for assigned oncology pharmaceutical / biological / drug-device combined products. · Responsible for safety surveillance, signal detection and risk management activities. · ...

The Associate Director supports the Global Safety Lead (GSL) for assigned oncology pharmaceutical / biological / drug-device combined products. · ...

The Associate Director of PV Sciences will support the Global Safety Lead for assigned oncology pharmaceutical/biological/drug-device combined products.Responsibilities include safety surveillance, signal detection, risk management activities.This role requires in-depth knowledge ...

The Associate Director supports the Global Safety Lead for assigned oncology pharmaceutical/biological/drug-device combined products. · ...

· Associate Director PV Sciences, Global Medical Safety Oncology is a Director-level position in the pharmaceutical manufacturing and biotechnology research industry.The ideal candidate will have a Bachelor of Science or Health Care Professional degree (e.g., RN, BSN, NP, PA, RP ...

Associate Director PV Sciences is responsible for safety surveillance and risk management activities. They support cross-functional assessment of benefit-risk profile and communicate safety information. · ...

Scientist Associate Director PV Sciences Global Medical Safety Oncology six months. · ...

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+Job summary · A Medical Director-Urologic Oncology position in Boston, · US.+ResponsibilitiesAct as Medical Monitor for ongoing Phase 2 oncology trials. · Ensure clinical data accuracy, safety reporting, and protocol compliance. · Collaborate with CROs and internal teams to supp ...

Hartman Young is working with an innovative biotech oncology company to support the appointment of a Pharmacovigilance (PV) Consultant. · ...

A well-funded biotech is seeking a Clinical Development Director with hands-on FIH–Phase II experience to advance its early-stage pipeline. · ...

The Clinical Research Associate (CRA) supports the planning and execution of oncology clinical trials. · Bachelor's degree/Master's degree in Life Sciences or related field (required) · ...

We are hiring a Travel Nurse - RN in Oncology for a rewarding opportunity. · Provide specialized nursing care to oncology patients, · ensuring safety and comfort. Administer treatments, · medications and monitor patient responses. · ...

We're partnering with a leading Boston-based oncology biotech to find a Senior Director of Regulatory Affairs to lead global regulatory strategy across their clinical development pipeline. · ...

The Clinical Research Associate (CRA) will support the planning, execution,and monitoring of oncology clinical trials in compliance with ICH-GCP,FDA regulations,and company SOPs. · Bachelor's degree/Master's degree in Life Sciences,Nursing, · or a related field (required) · , 2+ ...

We are hiring a dedicated Travel Nurse - RN in Oncology for a rewarding opportunity in Boston MA offering competitive pay travel accommodations health insurance and professional support. · Administer treatments monitor patient progress and collaborate with multidisciplinary teams ...

We are seeking a dedicated Travel Nurse RN - Oncology to join our team in Boston, MA. · Provide specialized nursing care to oncology patients, including administering treatments and monitoring responses. · Aess patient conditions, develop care plans, and educate patients and fami ...

The Global Head of Pharmacovigilance and Safety Science is a strategic leadership role responsible for medical, strategic, and operational oversight of drug safety. · Develop and execute the overall drug safety and pharmacovigilance (PV) strategy aligned with company and global r ...

We are seeking a dedicated · Locum Physician (MD/DO) specializing · in Hematology and Oncology. · Providing comprehensive patient care · Diagnosing and managing hematologic · and oncologic conditions, · ...

The Clinical Research Associate (CRA) will support the planning, execution, and monitoring of oncology clinical trials in compliance with ICH-GCP, FDA regulations, and company SOPs. · Key Responsibilities: Conduct site qualification, initiation, monitoring ,and close-out visits f ...