Msp Program Manager Jobs in Massachusetts (NOW HIRING)

Cambridge, US; Central Plains, US; Gaithersburg, US; Great Lakes East, US; Mid-Atlantic North, US; Mid-Atlantic South, US; New England, US; New Jersey, US; North Central, US; Pacific Northwest, US | full time | Job ID: 11471
About the role
The Medical Safety Physician (MSP) plays a vital role in supporting the oncology therapeutic area by providing medical safety expertise to one or more study management teams. In collaboration with assigned Safety Scientists, the MSP ensures patient safety throughout the clinical trial process. Responsibilities include contributing to clinical trial protocols, training investigators, assessing safety data (e.g., adverse events of special interest and serious adverse events), determining necessary follow-up actions, and conducting safety signal detection and evaluation. The MSP also ensures compliance with Good Clinical Practice (GCP) and regulatory reporting requirements, while contributing to essential safety documents such as Development Safety Update Reports (DSURs), updates to reference safety information, Investigator Brochures, and Clinical Trial Reports. This position offers the opportunity to take on a strategic role within the Medical Safety Pharmacovigilance (MSPv) department.
Your Contribution

• Accountable for the quality performance of one or more safety management team(s) (SMTs)
• Oversees safety monitoring, signal management, and the benefit-risk of assigned products through the product life cycle
• Identifies and leads escalation, management, and communication of safety inquiries and concerns for assigned products
• Formulates and drives the optimal safety strategy for assigned oncology programs in clinical development at the portfolio level
• Presents and interacts with Regulatory Authorities on safety matters
• Oversees quality content of the safety contributions to clinical and regulatory documents such as briefing book for regulatory authority meetings, investigator's brochure, clinical study report safety conclusion section, responses to regulatory authority inquiries, and other clinical/regulatory documents as needed
• Participates in due diligence for BioNTech's Licensing /Acquisition initiatives
• Represents MSPv in Alliance management projects such as safety data exchange agreement negotiations; or joint oversight committees with development partners, and/or other collaborative development projects
• Serves as safety subject matter expert at the portfolio level and is the arbiter for safety-related issues in any of its constituting programs
• Ensures activities are performed in compliance with applicable law, global and local regulations, and in accordance with internal and external quality standards
  Trains and mentors Safety Physicians and Safety Scientists

A good match

• Medical Degree (or internationally recognized equivalent). A MD/PhD and/or certified training in a relevant medical discipline is a plus.
• Extensive drug safety/pharmacovigilance experience within the biopharmaceutical/biotechnology industry that includes the development of innovative drugs, BLA/MAA submissions, and advisory committee experience, preferably in immuno-oncology/inflammation therapeutic area(s)
• Exposure to, or direct experience in working with Regulatory Agencies on development strategies for innovative oncology products, particularly those of US
• Has achieved demonstrable results in a matrix organization and in a multidisciplinary team, experience in implementing GCP standards in clinical trials, in particular safety reporting in compliance with global and local regulations

Your benefits and remuneration:
If the position is filled in the US, the Expected Pay Range is $168,100/year to $268,700/year + benefits, annual bonus & equity (bonus and equity is variable and dependent on company and individual performance). Compensation for the role will depend on several factors, including responsibilities of the job, education, experience, knowledge, skills, and abilities.
Compensation at other locations may vary significantly.
BioNTech is committed to the wellbeing of our team members and offers a variety of benefits in support of our diverse employee base. We offer competitive remuneration packages which is determined by the specific role, location of employment and also the selected candidate's qualifications and experience.
Note: The availability, eligibility and design of the listed benefits may vary depending on the location. The final requirements for the individual use of our benefits are based on the company's internal policies and applicable law.
How to apply:
Apply now by sending us your application documents including Curriculum Vitae, copy of ID, copies of degree certificates and professional certificates, motivation letter as well as your contact details via our online form.
Please note:
Only applications sent via our online form shall be considered. By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider 'HireRight'. You will be informed accordingly by your BioNTech-Recruiter.
We are looking forward receiving your application.
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