$171K - $231K/yr
Solid leadership and extensive experience either as direct line manager (required for those with ... Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are ...
$171K - $231K/yr
Solid leadership and extensive experience either as direct line manager (required for those with ... Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are ...
Irvine, CA · On-site
... clinical research study management * Demonstrated leadership and experience with working with cross-functional internal teams * Experience in: drug, device, interventional and non-interventional ...
Irvine, CA · On-site
... clinical research study management * Demonstrated leadership and experience with working with cross-functional internal teams * Experience in: drug, device, interventional and non-interventional ...
Westminster, CO · On-site
$146K - $210K/yr
A typical day will include- managing study initiation through close-out and supporting activities ... non-disqualifying physical or mental disability, national origin, veteran status or any other basis ...
Westminster, CO · On-site
$146K - $210K/yr
A typical day will include- managing study initiation through close-out and supporting activities ... non-disqualifying physical or mental disability, national origin, veteran status or any other basis ...
Austin, TX · On-site
$83K/yr
Non-Exempt from FLSA ---- Earliest Start Date: Immediately ---- Position Duration: Expected to ... Manage study start-up activities, including obtaining study materials and ensuring required ...
Austin, TX · On-site
$83K/yr
Non-Exempt from FLSA ---- Earliest Start Date: Immediately ---- Position Duration: Expected to ... Manage study start-up activities, including obtaining study materials and ensuring required ...
Translate protocols and study assumptions into demand forecasts across scenarios; communicate risks, constraints, and recommendations to stakeholders * Oversee clinical labeling strategy and ...
Translate protocols and study assumptions into demand forecasts across scenarios; communicate risks, constraints, and recommendations to stakeholders * Oversee clinical labeling strategy and ...
Boston, MA · On-site
The Role We're looking for a Senior Clinical Trials Manager who will own the end-to-end execution ... Own clinical study execution from protocol development through final study report -- including ...
Quick apply
Boston, MA · On-site
The Role We're looking for a Senior Clinical Trials Manager who will own the end-to-end execution ... Own clinical study execution from protocol development through final study report -- including ...
Austin, TX · On-site
$83K/yr
Senior Clinical Research Nurse The Senior RN Clinical Research Coordinator coordinates and ... The position independently manages day-to-day study operations and participant-facing research ...
Austin, TX · On-site
$83K/yr
Senior Clinical Research Nurse The Senior RN Clinical Research Coordinator coordinates and ... The position independently manages day-to-day study operations and participant-facing research ...
Acts as a model and coaches staff in effective verbal, non-verbal and written communication, which ... Manages study quality assurance and actively participates in quality assurance program for research ...
Acts as a model and coaches staff in effective verbal, non-verbal and written communication, which ... Manages study quality assurance and actively participates in quality assurance program for research ...
The Senior Clinical Trial Manager will independently manage all components of a clinical trial ... Independently lead Study Management Team(s), including cross-functional team(s), CRO(s) and third ...
The Senior Clinical Trial Manager will independently manage all components of a clinical trial ... Independently lead Study Management Team(s), including cross-functional team(s), CRO(s) and third ...
PURPOSE The Senior RN Clinical Research Coordinator coordinates and implements complex clinical ... Manage study start-up activities, including obtaining study materials and ensuring required ...
PURPOSE The Senior RN Clinical Research Coordinator coordinates and implements complex clinical ... Manage study start-up activities, including obtaining study materials and ensuring required ...
Acts as a model and coaches staff in effective verbal, non-verbal and written communication, which ... Manages study quality assurance and actively participates in quality assurance program for research ...
Acts as a model and coaches staff in effective verbal, non-verbal and written communication, which ... Manages study quality assurance and actively participates in quality assurance program for research ...
The Senior Supervisor, Post-Market Surveillance (PMS) and Post-Market Clinical Follow-up (PMCF ... Prior clinical study management or clinical research experience strongly preferred, particularly ...
The Senior Supervisor, Post-Market Surveillance (PMS) and Post-Market Clinical Follow-up (PMCF ... Prior clinical study management or clinical research experience strongly preferred, particularly ...
Middleton, WI · On-site
With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for ... The Senior Study Lead is accountable for managing quality records and ensuring strict adherence to ...
Middleton, WI · On-site
With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for ... The Senior Study Lead is accountable for managing quality records and ensuring strict adherence to ...
Boston, MA · On-site
The Opportunity The Senior Clinical Trial Manager (CTM) plans and manages overall activities for ... Contribute to the reporting of clinical studies and clinical documentation to regulatory ...
Boston, MA · On-site
The Opportunity The Senior Clinical Trial Manager (CTM) plans and manages overall activities for ... Contribute to the reporting of clinical studies and clinical documentation to regulatory ...
Zebulon, NC · On-site
As part of the Study Team Operating model (STOM), you will act as the primary interface between ... Serve as the primary supply chain interface with the clinical study team (Global Study Manager/Lead ...
Zebulon, NC · On-site
As part of the Study Team Operating model (STOM), you will act as the primary interface between ... Serve as the primary supply chain interface with the clinical study team (Global Study Manager/Lead ...
... clinical care for patients; making our communities healthier and stronger; preparing tomorrow ... Jefferson Health Plans is a not-for-profit managed health care organization providing a broad range ...
... clinical care for patients; making our communities healthier and stronger; preparing tomorrow ... Jefferson Health Plans is a not-for-profit managed health care organization providing a broad range ...
Durham, NC · On-site +1
Provide leadership and direction to clinical site management team members from study start through to closure * Serve as Site Management's primary point of contact and representative for clinical ...
Durham, NC · On-site +1
Provide leadership and direction to clinical site management team members from study start through to closure * Serve as Site Management's primary point of contact and representative for clinical ...
Boston, MA · On-site +1
$90K - $110K/yr
As a Clinical Study Operations Manager within the Clinical Study Operations team, you will be responsible for ensuring the successful operational delivery of Beacon's clinical studies, from startup ...
Boston, MA · On-site +1
$90K - $110K/yr
As a Clinical Study Operations Manager within the Clinical Study Operations team, you will be responsible for ensuring the successful operational delivery of Beacon's clinical studies, from startup ...
... Manager DePuy Synthes is recruiting for a Clinical and Pre-Clinical QA Compliance Manager, to ... This role will support the clinical study design, execution, documentation, and oversight in ...
... Manager DePuy Synthes is recruiting for a Clinical and Pre-Clinical QA Compliance Manager, to ... This role will support the clinical study design, execution, documentation, and oversight in ...
The Sr. Manager Clinical Research Engineering uses their in-depth clinical, scientific, and ... Lead and execute early-stage feasibility, pilot, and pivotal studies to support technology ...
The Sr. Manager Clinical Research Engineering uses their in-depth clinical, scientific, and ... Lead and execute early-stage feasibility, pilot, and pivotal studies to support technology ...
$22K - $38.7K
1% of jobs
$38.7K - $55.5K
3% of jobs
$55.5K - $72.2K
7% of jobs
$87.1K is the 25th percentile. Wages below this are outliers.
$72.2K - $88.9K
15% of jobs
$88.9K - $105.6K
9% of jobs
$105.6K - $122.4K
14% of jobs
The median wage is $123.4K / yr.
$122.4K - $139.1K
17% of jobs
$150.9K is the 75th percentile. Wages above this are outliers.
$139.1K - $155.8K
13% of jobs
$155.8K - $172.5K
11% of jobs
$172.5K - $189.3K
7% of jobs
$189.3K - $206K
3% of jobs
$22K
$125.3K
$206K
For Non Clinical Study Manager Senior Study Manager jobs, the most frequently searched job titles are:
Remote
$171K - $231K/yr
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 22 days ago
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
Line management responsibilities:
Provides leadership, management, and/or mentorship to associate directors, clinical study managers at various levels for assigned portfolio
Collaborates effectively with internal and external stakeholders within the region as well as with global stakeholders to ensure the needs of the business are met.
Drives resourcing and capability development related to regional study management
Ensures alignment of regional resources and deliverables with overall portfolio goals
Essential Functions of the job:
Regional Leadership
Line management responsibilities:
Provides leadership to the team of Associate Directors, Operations Managers and Operations Associates in charge of regional study management, including mentoring, coaching and managing performance.
Collaborates with peers in the regional Clinical Operations leadership team to ensure smooth delivery of all trials in the region on time, with quality and in line with the broader organizational goals.
Liaises and collaborates as required with external, global and/or regional stakeholders such as e.g., FSP partners, clinical operations leaders in other regions, and monitoring heads in key countries in the region.
Drives the overall Clinical Operations strategy for the region and has accountability for performanceagainst key metrics.
Drives the development of initiatives and ensures that novel ideas on how to deliver on clinical trials are generated and considered.
Quality
Line management responsibilities:
Ensures team members are trained on and are adhering to required processes and SOPs.
Drives a quality mindset in the regional study management organization and supports the proactive implementation of risk management principles in the regional study management organization.
Sets clear quality expectations for the regional study management organization.
Drives the knowledge management and continuous improvement process by ensuring information is captured, retained, and leveraged in future work.
Budget and Resources
Line management responsibilities:
Contributes to the resourcing process for regional study management. Ensures efficient resourcing addressing both study needs as well as individual development needs through the principle of assigning the right person to the right study at the right point in time.
Supervisory Responsibilities:
Line management responsibilities:
Conducts performance appraisals for direct reports which includes providing feedback
Supports set up of development plans for direct reports
Drives the hiring of new talent into the regional study management organization
Computer Skills:
MS Office, Project Planning Applications
Other Qualifications:
Solid leadership and extensive experience either as direct line manager (required for those with line management responsibilities) or as cross functional team lead
Strong written and verbal communication skills
Exercises sound judgement and discretion in matters of significance
Ability to work independently and effectively handle multiple priorities in a fast-paced environment
Excellent interpersonal skills, strong organizational skills and ability to influence and lead
Travel:
Travel might be required as per business need.
Education & Experience Required: Bachelor's degree in a scientific or healthcare discipline and 10+ years of progressive experience in clinical operations within biotech, pharmaceutical or CRO industry. Preferably master's degree in a scientific or healthcare discipline and 7+ years of progressive experience in clinical operations within biotech, pharmaceutical or CRO industry.
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.
