20 Best senior clinical manager jobs in Boston, MA (Hiring Now!)

Clinical Project Manager
Ipsen Bioscience, Inc. —Cambridge, MA
Work with the SP, Patient Affairs office, and digital team as appropriate to develop and approve a recruitment strategy and communication tools (e.g. Newsletter…
$112,500 - $165,000 a year
Senior Implementation Manager
Movable Ink —Waltham, MA
Day to day point person and Project Manager for launching new clients, communicating and collaborating throughout the implementation, and holding regularly…
$90,000 - $105,000 a year
Quick Apply
8d
Senior Manager, Lab Operations
Generate Biomedicines —Somerville, MA
BSc/MSc in a science/engineering field (Biology, Chemistry, Biotechnology, etc.). Vendor and Contractor Coordination: Manage relationships with external vendors…
Estimated: $118K - $149K a year
10d
Senior Property Manager - Boston, MA
Trinity Management LLC —Boston, MA
A successful candidate must have a strong property management background that includes rent collections/enforcements, recertifications, budgeting, financial…
Estimated: $82.6K - $105K a year
Quick Apply
3d
RN/VNA, Clinical Case Manager 5 yrs Visiting Nursing Experience
Beneficence Home Healthcare —Milton, MA
Must have a RN license (Required). Currently, licensed “in good standing” in the state where skilled home visits will be provided.
$118,429 - $135,000 a year
Quick Apply
Senior Operations Manager, Urgent Care - South Region
Mass General Brigham Medical Group —Somerville, MA
They will be responsible for collaborating with their local clinical leaders for establishing an environment of continuous improvement of operational and…
Estimated: $120K - $152K a year
10d
Sr. Manager of Search
ZoomInfo Technologies LLC —Waltham, MA
Skills: Strong understanding of search engine algorithms, technical SEO, content marketing, and web analytics tools (e.g., SEMRush, Google Analytics).
$122,400 - $168,300 a year
Quick Apply
13d
Executive Assistant & Project Manager
Somerville Cambridge Elder Services —Somerville, MA
Provide hospitality to all guests and help to create a welcoming environment. The Executive Assistant acts as a business partner and provides high-level…
$60,000 - $65,000 a year
Quick Apply
Senior Inventory Manager
Boston Dynamics —Waltham, MA
BA/BS degree in related field (supply chain, business, industrial engineering, etc.) preferred or equivalent experience. Conduct inventory audits as required.
Estimated: $88.8K - $113K a year
10d
Senior Manager, Corporate Strategy
Thermo Fisher Scientific —Waltham, MA
Master’s degree in business, life sciences, or related field. 4+ years of relevant professional experience, including broad-based experience in strategy and…
Estimated: $94.8K - $120K a year
7d
Senior Customer Success Manager
Login VSI —Boston, MA
Time Zone: Ability to cover meetings and calls with customers in Europe. The primary role of the Senior Customer Success Manager (CSM) is to own the post-sales…
Estimated: $97.1K - $123K a year
Quick Apply
6d
Senior Program Manager
MYROBALAN THERAPEUTICS, INC. —Medford, MA
Strong written and verbal communication skills and the ability to develop and deliver clear and concise presentations for stakeholders and partners.
Estimated: $128K - $163K a year
Quick Apply
Senior Manager, Delegation and Facility Enrollment
Mass General Brigham —Somerville, MA
Research operational and system issues identified by other RCO departments and develop/implement solutions for performance improvement.
Estimated: $110K - $139K a year
Senior AI Commercial Strategy Manager
Cohere Health —Boston, MA
Deep expertise in ML including latest wave of LLMs; technical background preferred in AI/ML/data science. In accordance with state applicable laws, Cohere is…
$150,000 - $170,000 a year
Quick Apply
8d
Senior Manager GLP/GCP Veeva Doc Control and Training
Sana Biotechnology. —Cambridge, MA
We are committed to providing a workplace free of discrimination and harassment based on race, color, religion, age, gender, national origin, ancestry, physical…
$160,000 - $200,000 a year
Senior HR / Generalist Manager
Science from Scientists —Woburn, MA
Bachelor’s degree in HR, business, or related field preferred. Ensure legal compliance of state and federal regulations and applicable employment laws.
$70,000 - $90,000 a year
Quick Apply
4d
Senior Performance Manager
Outsell Corporation —Boston, MA
Data analysis, and Collaboration skills. Effectively manage client portfolio of accounts to foster long-term strategic business relationships with our dealer…
Estimated: $84.7K - $107K a year
Quick Apply
Senior Manager, Clinical Trial Transparency and Disclosure
Cerevel Therapeutics, LLC —Boston, MA
Understands the clinical drug development process, including clinical trial design, operations and results analysis. Experience working with CTIS preferred.
Estimated: $137K - $173K a year
Sr. Global Program Manager
New Balance —Brighton, MA
Work closely with program sponsors, cross-functional teams, and assigned project managers to develop the scope, deliverables, required resources, work plan,…
Estimated: $122K - $155K a year
Senior Manager, Manufacturing Technical Operations
Vertex Pharmaceuticals —Boston, MA
This role will require some regional travel to our Cambridge and Providence manufacturing locations and ad-hoc flexibility to support our clinical cell…
Estimated: $143K - $181K a year

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Clinical Project Manager

Ipsen Bioscience, Inc. - Cambridge, MA

Apply Now

Job Details

Full-time $112,500 - $165,000 a year

Benefits

Commuter assistance
Disability insurance
Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Parental leave
Vision insurance

Qualifications

Microsoft Powerpoint
French
Microsoft Excel
EHS
Clinical research
English
3 years
Clinical trials
Good Clinical Practice
Research & development
Leadership
Communication skills
Adobe Acrobat

Full Job Description

Clinical Project Manager (CPM)

Purpose of the position

Oversee and drive all aspects of the assigned global international clinical study(ies) outsourced to a CRO in respect of planning/timelines, quality, budget and defined goals
Drive execution and report activities in conjunction with Clinical Development Program Directors (CDPDs), Medical Dev. Directors (MDDs), and other Ipsen team members
Endorse project plan developed by the CROs in accordance with study objectives and Ipsen requirements in terms of team responsibility, risk mitigation plan, escalation process, communication plan...
Ensure the Global clinical studies are managed according to Good Clinical Practice (GCP), local regulations, guidelines and SOPs in the required standard of quality
Communicate and share the progress of the project, and work effectively as a Team
Lead, Manage and Drive the cross-functional Clinical Study Team and Contract Research Organization (CRO) in collaboration with the CDPDs and Ipsen team members responsible of the study

Main responsibilities and tasks

Ensure study team management and communication

Oversee and drive cross-functional leadership and expertise to ensure effective contribution, execution and delivery of study activities as per quality, plan/timelines and budget
Foster a team approach to all activities associated with the implementation, conduct and closing of clinical studies including Ipsen clinical study team members (TA, Biometry, Pharmacovigilance, Finance controlling, Global Regulatory Affairs, CMC Supply chain…) and SPs
Establish and maintain excellent professional relationships with Services Providers, clinical study team through regular communication, between company, investigators and experts in conjunction with Medical Dev. Director (MDD) and other relevant Ipsen team members

Lead clinical project processes

Lead cross-functional clinical study teams focused on conduct of assigned projects
Interact with CDPD to define strategic operational direction
Review status reports provided by Service Provider/CRO and highlight issues to facilitate decision making
Manage and lead all operational aspects for implementation and conduct of global clinical trial activities from study start-up to CSR, in respect of GCPs and relevant SOPs

Key accountabilities and activities

Develop, manage, and execute assigned projects by:

Set-up study team before Services Provider are on board and lead and manage regular internal Study Team meetings during the course of the study.
Contribute to study protocol development including study concept where applicable
Develop and control planning and study timelines in collaboration with all other Ipsen supportive functions/SPs
Provide expertise to clinical outsourcing specifications and purchasing to facilitate RFP documents and selection of Services Provider
Participate in the selection of Services Providers and other external vendors in collaboration with purchasing department, study team, finance controller and Corporate Legal Affairs
Accountable for the development, management and tracking of trial budget working closely with the finances and service provider representative - financial management of the clinical trial including budget planning and preparation of quarterly reports
Ensure appropriate oversight of Services Providers) and other external vendors activities and develop the oversight manual in accordance with the services providers Technical Specifications document
Review final draft and approve major study documents as described in the Services Providers /CROs Technical Specification documents (e.g. oversight manual, communication plan, project plan, instruction manuals….)
Supervise country feasibility and site selection processes in collaboration with CDPD, MDD, GMA, CRO and Ipsen Affiliates (if needed) to identify and gain approval for high quality investigators and study sites
Provide support and oversee the activities of the Clinical Trial Associate (CTA) assigned to the study for: insurance certificate, contracts signature process, set-up and management of the Trial Master File (eTMF), transparency and local reporting as per legal and Ipsen requirements, update of reporting tools (study trackers, Hermes,…) and alert if required; drive billing and forecast
As applicable, provide support and oversee the activities of the Clinical Monitoring Lead (CML) to ensure the coordination of the clinical, monitoring and site management activities are in accordance with study objectives and quality standards.
Work with the SP, Patient Affairs office, and digital team as appropriate to develop and approve a recruitment strategy and communication tools (e.g. Newsletter…) to increase study awareness, patient recruitment and retention in the study
Ensure through study team management that the necessary regulatory, safety and data evaluation requirements are met to allow the conduct of clinical related activities in conjunction with the Regulatory, Pharmacovigilance (GPS), Data Management and Statistics Departments
Participate in meetings lead by SP (e.g. Inv. & CRA meeting, Study team meeting, Clinical Data Review …), Review meeting minutes and ensure with SP Project Manager that issues are proactively identified, communicated and resolved in a timely manner
Ensure timely and accurate completion of project milestones, study progress tools (planning reporting, study dashboard...) and escalate appropriately in case of deviation to the planning and of any issue regarding the quality of the data
Travel as needed to observe and discuss projects, build positive working relationships and maintain enthusiasm regarding projects
For activities, not out-sourced (e.g. Management of IMP…) ensure regular forecast update and bulk shipment
Work with line functions and Quality Assurance (GRDQ) to identify potential quality issues. Coordinate post quality audit hosted by Sponsor and ensure CAPA implementation by SP
Assist Quality Assurance (GDDQ) within inspections preparation as applicable
Participate in the preparation and review of clinical study reports and ensure that CSR Appendices are completed and validated by the relevant functions within the agreed timelines.
Liaise with the relevant Ipsen or Service Providers teams to ensure the posting of the clinical study and the results on the required registries and as per local regulations.
To perform any other activity as may reasonably be required by the DCDP and/or TA clinical operation head from time to time.

Clinical activities (out of studies)

Contribute/participate on SOP update and review training material created by Process Training Management
Contribute to the efficient operation of the TA Group and to transversal project cross- TAs and other departments within Ipsen (e.g. systems implementation, change management initiatives, continuous improvement initiatives …)

EHS responsibilities:

Comply with applicable EHS regulations and procedures.
Participate in the site's EHS performance by reporting risks, malfunctions or improvements
Participate in mandatory EHS training

Experience / Qualifications

Experience:

Relevant experience of pharmaceutical drug development:

Minimum of 3 years working in clinical research with management of clinical activities for the set up and running of international registrational studies, for at least 2 years
Experience in managing and developing relationships with Contract Research Organizations (CROs/SPs)
Experience in working with multidisciplinary groups (internal & external), flexibility, adaptability and ability skills to work within a matrix environment.

Qualification:

Life science or medical graduate or other relevant qualifications.

Language:

English: Very good English language knowledge (oral and written)

Key Required Technical Competencies

Ability to work in a strong regulated environment within a quality management system (QMS)
Advanced knowledge of software application (ex: Word, Excel, PowerPoint, Adobe Reader …)
Ability to organize and prioritize
Able to produce work in teams and within a multi-disciplinary environment
Basic Financial Knowledge- must be able to work with financial tracking tools
Knowledge of Pharmaceutical Industry R&D - Good understanding of the drug development process and knowledge of the pharmaceutical industry environment
Good knowledge of the Good Clinical Practices (GCP) or other clinical study regulations
Intimate knowledge of regulatory requirement (ICH E6, GCP, EU Directive)
Excellent leadership skills and capability to work within a team as leader and team player
Excellent organizational and management skills
Strong verbal and written communication skills (French, English)

The annual base salary range for this position is $112,500-$165,000.

This job is eligible to participate in our short-term incentives program.

At Ipsen we are proud to offer a comprehensive employee benefits package, including 401(k) with company contributions, group medical, dental and vision coverage, life and disability insurance, short- and long-term disability insurance, as well as flexible spending accounts. Ipsen also provides parental leave, paid time off, a discretionary winter shutdown, well-being allowance, commuter benefits, and much more.

The pay range displayed above is the range of base pay compensation within which Ipsen expects to pay for this role at the time of this posting. Individual compensation within this range depends on a variety of factors, including, but not limited to, prior education and experience, job-related knowledge and demonstrated skills.

Apply Now

senior clinical manager jobs in Boston, MA

Clinical Project Manager

Senior Implementation Manager

Senior Manager, Lab Operations

Senior Property Manager - Boston, MA

RN/VNA, Clinical Case Manager 5 yrs Visiting Nursing Experience

Senior Operations Manager, Urgent Care - South Region

Sr. Manager of Search

Executive Assistant & Project Manager

Senior Inventory Manager

Senior Manager, Corporate Strategy

Senior Customer Success Manager

Senior Program Manager

Senior Manager, Delegation and Facility Enrollment

Senior AI Commercial Strategy Manager

Senior Manager GLP/GCP Veeva Doc Control and Training

Senior HR / Generalist Manager

Senior Performance Manager

Senior Manager, Clinical Trial Transparency and Disclosure

Sr. Global Program Manager

Senior Manager, Manufacturing Technical Operations

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