Top 296 site budget manager pharmaceutical Jobs in remote

Clinical Trial Manager, Clinical Operations
Spyre Therapeutics —Remote
- $135,000 - $155,000 a year
- Remote
- 5 years
- Bachelor of Science
- Organizational skills
- Health insurance
- Retirement plan
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Clinical Trial Associate/Sr. Clinical Trial Associate, Clinical Operations
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Penumbra —Remote
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- 5 years
- English
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Senior Clinical Trials Associate
BioAge Labs —Remote
- $0 a year
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Senior Oncology Account Manager, Nashville
Jazz Pharmaceuticals —Nashville, TN
- $155,200 - $232,800 a year
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Jazz Pharmaceuticals —Atlantic City, NJ
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Senior Oncology Account Manager, Nashville
Jazz Pharmaceuticals —Birmingham, AL
- $155,200 - $232,800 a year
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Jazz Pharmaceuticals —Baltimore, MD
- $176,800 - $265,200 a year
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- 3 years
- Master's degree
- Bachelor's degree
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Regional Sales Manager, Sleep – Mid-Atlantic Territory
Jazz Pharmaceuticals —Philadelphia, PA
- $176,800 - $265,200 a year
- Remote
- 3 years
- Master's degree
- Bachelor's degree
- Health insurance
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Senior Oncology Account Manager- Philadelphia, PA & Southern New Jersey (Remote)
Jazz Pharmaceuticals —Philadelphia, PA
- $155,200 - $232,800 a year
- Remote
- Bachelor's degree
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- Senior level
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Senior Oncology Account Manager - Northern New Jersey
Jazz Pharmaceuticals —Trenton, NJ
- $155,200 - $232,800 a year
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- Writing skills
- Bachelor's degree
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4d
Sales Manager -Midwest
PEXCO —Ohio
- Remote
- Windows
- Bachelor's degree
- Senior level
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Senior Oncology Account Manager - Northern New Jersey
Jazz Pharmaceuticals —Newark, NJ
- $155,200 - $232,800 a year
- Remote
- Writing skills
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4d
Senior Director, Clinical Operations
Syncromune —Remote
- $250,000 - $275,000 a year
- Full-time
- Background check
- 11+ years
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Clinical Project Manager I - Ophthalmology
Voiant Clinical —Remote
- $65,000 - $80,000 a year
- Full-time
- Remote
- Background check
- Mid-level
- High school diploma or GED
- Health savings account
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2d
Senior Project Manager, Clinical Trials
Cogstate —Remote
- $125,000 - $135,000 a year
- Full-time
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- 7 years
- Computer Science
- Paid holidays
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Manager, Site Budgets & Contracts, Clinical Operations
Agios Pharmaceuticals —Remote
- $110,000 - $165,000 a year
- Remote
- 3 years
- Bachelor's degree
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Senior Account Manager
Force Communications —Remote
- $95,000 - $115,000 a year
- Full-time
- 3 years
- Presentation skills
- Bachelor's degree
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Learning Advisor - Contract
サイネオス・ヘルス —Remote
- $60 - $70 an hour
- Full-time
- Remote
- Management
- Writing skills
- Microsoft Office
- Paid time off
- 401(k) matching

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site budget manager pharmaceutical jobs near remote

Clinical Trial Manager, Clinical Operations

Spyre Therapeutics -
Remote

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Job Details

$135,000 - $155,000 a year
9 days ago

Benefits

Health insurance
Unlimited paid time off
Retirement plan

Qualifications

Pharmaceutical company experience
Pharmaceutical research

Full Job Description

Spyre Therapeutics is a clinical-stage biotechnology company committed to developing next-generation therapies that elevate the standard in immunology by delivering more complete disease control, greater durability, and a simpler treatment experience for patients. Spyre's pipeline includes investigational extended half-life antibodies targeting α4β7, TL1A, and IL-23.

Role Summary:

The Clinical Trial Manager (CTM) is a pivotal role responsible for the management of Clinical Trials from vendor selection through Clinical Study Report (CSR) completion. The CTM will organize and supervise clinical trials, ensuring they meet all company and regulatory requirements. The CTM will collaborate closely with internal R&D team members in addition to external CRO partners to drive successful trial execution to advance the development of our cutting-edge antibody conjugate portfolio ensuring efficacy, safety, and regulatory success.

Key Responsibilities:

Responsible for the management of Clinical Trials from vendor selection through Clinical Study Report (CSR) completion.
Ensure clinical trial activities are completed on time, within budget and in a highly dynamic and complex environment in accordance with appropriate quality standards including ICH/GCP requirements.
Create and implement study-specific clinical monitoring tools and documents, including informed consent development and EU CTR.
Lead the identification, evaluation, selection, and oversight of clinical trial sites.
Author and implement operational plans to ensure efficient study enrollment and high-quality monitoring activities at clinical sites.
Review/approve vendor and site invoices and track study budget to forecast, working closely with finance and clinical business operations.
Responsible for implementation and oversight of Trial Master File for inspection readiness.
Drive overall process and provide support to cross-functional teams in the development of study documents including study protocols, consent forms and budget templates.
Serve as lead in the creation of project plans, logs, templates, newsletters, and other documents.
Review and approve site specific documents (such as informed consent forms, site budgets, monitoring reports) along with other relevant project team members.
Provide study updates and reports, inclusive of study risks and issues.
Lead internal and external meetings for assigned clinical trial(s), including Investigator Meetings, conferences, events and study management meetings.
Responsible for ongoing study data reviews and data cleaning activities.
Provide oversight of CTA and CRA activities such as site identification, qualification, selection, initiation, data quality, sample tracking, interim monitoring and close out activities.
Manage trial-level quality risk management.
Oversee study supplies management.
Support the development and complete the delivery of study training to investigators, site staff and internal staff on study processes.
Participate in the preparation and follow up of internal process audits, vendor, and study site quality audits as well as regulatory inspections.
Other duties as assigned.

Ideal Candidate:

B.A./B.S. in life sciences or equivalent
A minimum of 5 years of clinical research experience within the pharmaceutical or biotechnology industry, with at least 2+ years managing early phase clinical trials; managing global clinical trials a plus
Inflammation and/or Immunology experience is strongly preferred
Strong working knowledge of clinical operations and experience with clinical study conduct from start-up through close-out
Informed consent development and EU CTR experience
Ability to lead cross functional study teams in a matrix organization
Working knowledge of FDA/ICH guidelines and industry/technology standard practices including Good Clinical Practices; trial initiation and management practices and procedures
Excellent communication and interpersonal skills, with the ability to lead and motivate teams and collaborate effectively across functions.

What We Offer:

Opportunity to work in a fast-paced, dynamic environment where you help shape the culture of our young company, contribute broadly to advance meaningful medicines, and learn quickly.
Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits.
Unlimited PTO
Two, one-week company-wide shutdowns each
Commitment to provide professional development opportunities.
Remote working environment with frequent in-person meetings to address complex problems and build relationships.

The expected salary range offer for this role is $135,000 to $155,000. Actual pay offered may vary depending on job related knowledge, experience, education, and geographic location.

As an equal opportunity employer, Spyre is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment designed to create a stronger and better Spyre that is focused on developing life-changing products for patients.

Spyre Therapeutics, along with other biotech companies, has become aware of a surge in email scams targeting prospective job candidates within our industry. Please be aware that official recruiters at Spyre Therapeutics only use email addresses with the domain "@spyre.com." We want to also emphasize that we never request candidates to make any purchases or divulge sensitive personal information via email.

Please also be aware that all job postings will be listed on our website at spyre.com/careers/.

Apply Now

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