Biogen

Director, Business Performance Management

Posted on: 18 Jan 2021

Cambridge, MA

Job Description

Job Description

Summary :

This is role is the Head of Business Performance Management (BPM) group within Global Clinical Operations (GCO) POC (Performance Operational Capabilities) group. This is a key strategic and leadership role in support of identifying, developing and measuring performance & improvements to working practices across Global Clinical Operation (GCO), potentially touching all employees of the organization including, our external stakeholders (investigator sites, patients and partners).

The BPM group, in support of GCO, focuses on identifying, reporting and effectively displaying key performance indicators (KPIs), metrics, & insights (~ business analytics), oversight of GCOs clinical systems & technology needs, resource and demand management, provides expertise on continuous improvement (CI) methodologies, and provides project management support for initiatives as needed. The role is accountable and responsible to lead and oversee all of the remits within BPM.

Given scope and business needs, the role may require heightened focus/specialization in one or more of the other areas within Business Performance Management at any given time.

Job Description :

The role is responsible for the following key job duties -

Lead and provide direction to the business analytics strategy for GCO. Responsible to build the capabilities and ensure execution per plan for identifying, reporting, and effectively displaying key performance indicators (KPIs), metrics, & insights

o Identify internal and external performance measures. Continually keep up to date with industry insights and intelligence to support identification of leading and lagging indicators

o Identify and manage a robust and fit for purpose reporting capability

o Identify operational data quality issues and a strategy and plan to maintain operational data quality at high standards

o Share performance measures to inform continuous improvement efforts

o Identify & execute on opportunities with external vendors (CROs, data providers, technology vendors) that would support GCOs business analytics goals and lead and oversee such efforts

Responsible to oversee GCOs key clinical information systems and technology capabilities and needs

o Provide expert advice and direction to the clinical information systems strategy for GCO. Identify opportunities for innovation

o Ensure proper day to day functioning of GCOs key clinical information systems (e.g Clinical Trial Management Systems (CTMS), Interactive Response Technologies (IRT), Operational Data Repository (ODR), etc.) and address issues in an expeditious manner to avoid business continuity disruption

o Liaise with other business system owners (e.g Clarity) to ensure GCO needs are met as well as to ensure GCOs system strategy is in alignment with other functions (Clinical Sciences, R&D).

o Champion and advocate for GCOs IT needs with personnel and leadership from the Information Technology (IT) dept (e.g IT Functional Lead). Liaise with IT on GCOs IT projects to ensure challenges and opportunities are addressed

o Coordinate and be the lead representative for GCOs IT Technology Annual Operating Plan (AOP)

Responsible for GCOs resource and demand management processes and reporting

o Lead GCOs resource & demand management processes & practices to allow for effective reporting on employee and contractor staff resource assignments and demand needs. Identify opportunities for improvement in our resource and demand management practices and process to help better support data driven justifications for resources to meet business needs

o Be the lead point of contact for other stakeholders in R&D (and beyond) to align processes and data as it relates to resource and demand management

o Provide expert advice, guidance and training (as appropriate) to GCO on systems and processes used in resource and demand management

Lead, support process improvement and project management needs (for non clinical program/study initiatives) needs within GCO.

o Provide expert guidance and/or facilitation for process improvement methodology on initiatives to meet GCO goals/vision. Build and ensure fit for purpose framework for lessons learned and After Action Review (AARs) that aligns with R&D strategy as needed.

o Build and ensure capability (e.g. via employees, contractors, and/or consultants) to support GCOs project management needs for non-clinical program/study initiatives

o Track and manage the GCO goals and portfolio of process improvement initiatives within GCO to allow for accurate and period reporting of statuses

As a member of the POC leadership team, and as an extended member of GCO Senior Leadership Team (GCO XLT) provide consultative and strategic advice into the overall remit of GCO, POCs and BPMs vision and mission in support of clinical program and study execution. Participate in BPM and POC LT mtgs and extended GCO Senior Leadership Team (XLT) meetings

Provides group leadership, management, and guidance to direct reports. Oversee contractor staff and ensure services/deliverables and SLAs are met. For employee staff is responsible for conducting performance management, career development, and compensation planning within the remit / department. Responsible for overall team build out, attracting and retaining talent, recruiting internal staff and external contractors to support team goals.

Qualifications

10 - 15+ years of experience in the pharmaceutical, biotech and/or management consulting industry.

Proven leadership ability and team building skills are critical. Robust expertise and experience in project management & portfolio management, and strong facilitation skills are critical to fulfilling the requirements of this role.

Sigma Black or Green Belt certification and knowledge of lean and other continuous improvement methodologies is a plus.

Education :

Bachelor's Degree required and Masters degree highly preferred.

Additional Information

All your information will be kept confidential according to EEO guidelines.

Biogen

Cambridge, MA

Biogen Inc. discovers, develops, manufactures, and delivers therapies for treating neurological and neurodegenerative diseases worldwide. The company offers TECFIDERA, AVONEX, PLEGRIDY, TYSABRI, and FAMPYRA for the treatment of multiple sclerosis (MS); SPINRAZA for the treatment of spinal muscular atrophy; and FUMADERM for the treatment of plaque psoriasis. It also provides BENEPALI, an etanercept biosimilar referencing ENBREL; FLIXABI, an infliximab biosimilar referencing REMICADE; and IMRALDI, an adalimumab biosimilar referencing HUMIRA. In addition, the company offers RITUXAN for the treatment of non-Hodgkin's lymphoma, chronic lymphocytic leukemia (CLL), rheumatoid arthritis, two forms of ANCA-associated vasculitis, and pemphigus vulgaris; RITUXAN HYCELA for non-Hodgkin's lymphoma and CLL; GAZYVA to treat CLL and follicular lymphoma; and OCREVUS for the treatment of primary progressive MS and relapsing MS, and other anti-CD20 therapies.

Further, it is involved in developing BIIB098, Opicinumab, and BIIB061 for MS and neuroimmunology; Aducanumab, Elenbecestat, BAN2401, BIIB092, BIIB076, and BIIB080 to treat Alzheimer's disease and dementia; BIIB092 and BIIB054 for treating Parkinson's disease and movement disorders; BIIB067, BIIB078, and BIIB110 to treat neuromuscular disorders; BIIB093, TMS-007, and Natalizumab to treat acute neurology; BIIB104 for treating neurocognitive disorders; BIIB074 and BIIB095 for pain; and Dapirolzumab pegol, BG00011, and BIIB059 for treating other diseases, which are under various stages of development.

The company offers products through its sales force and marketing groups. Biogen Inc. has collaboration agreements with Genentech, Inc., Eisai Co., Ltd., Alkermes Pharma Ireland Limited, Bristol-Myers Squibb Company, Acorda Therapeutics, Inc., AbbVie Inc., C4 Therapeutics, University of Pennsylvania, Applied Genetic Technologies Corporation, and others. The company was founded in 1978 and is headquartered in Cambridge, Massachusetts.

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