Skip to content

Open nowPosted 6 days ago

Senior Director, Project Quality

Workable (global search)108,016 open roles

Where
United States
Work mode
Remote
Get the CV for this job

From $25 per CV, paid once. No subscription.

Your applicationOpen nowSenior Director, Project QualityWorkable (global search) · United States
  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on Workable (global search)'s own form.

The reply lands in your private mailbox

3×more interviews than doing it yourself with ChatGPT.

The clock on this job

Early applications get read.

7.9% of postings close within 7 days. Measured by our own scanner across the market. Workable (global search) postings stay open a median of 7 days.

Share of postings closed within
  1. 1.6%1 day
  2. 3.6%3 days
  3. 7.9%7 days
  4. 14.9%14 days
  5. 34.0%30 days
This job: posted 6 days ago

Workable (global search) median: 7 days open

The posting

Flourish Research is where clinical trials thrive. Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!

Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.

We are actively hiring a Senior Director, Project Quality for our Operational Quality division.

Shift: Monday-Friday day shift (40 hours per week) Location: Remote FLSA Classification: Exempt

Job Title: Senior Director, Project Quality

PURPOSE: Main point of contact and subject matter expert for all project quality functions across all sites owned and operated by Flourish Research. This includes, but is not limited to, managing and overseeing the Flourish QMS, driving and delivering operational quality and improvement initiatives, managing the Project Quality team, consulting on quality, risk and regulatory compliance, and monitoring project quality compliance.

ESSENTIAL JOB FUNCTIONS:

A. Build, implement, and manage a companywide QMS; create controlled documents to support and maintain the QMS and its requirements.

B. Initiate and lead required QMS reviews per the Flourish Quality Manual.

C. Research, implement, and manage an eQMS solution for all sites.

D. Support site heads/site directors to establish quality compliance and ensure maintenance of process.

E. Create a Project Quality team – determine needs, qualifications, requirements, training, and processes.

F. Lead/support Project Quality team in execution of quality management processes across all sites (quality management plans, risk and QI management, Quality Evaluations, etc.).

G. Collaborate with Process Quality on quality-related process improvements.

H. Provide support to the business on quality matters to ensure regulatory compliance and achievement of commercial objectives, including quality offerings to sponsors (e.g., QTLs, CTQ factors, quality agreements).

I. Provide guidance and insight on SOP harmonization initiative, ensuring compliance of SOPs with the latest regulatory standards and guidance.

J. Report regularly to site staff quality performance feedback, metrics, reported QIs and CAPAs.

K. Provide guidance and follow-up on QIs and CAPAs to operational staff.

L. Support Project Quality team in using eQMS for study quality management.

M. Collaborate with Support Services regarding quality related aspects of new site integration and vendor management.

N. Lead and prepare sites for sponsor audits and inspections. Support physicians and site leaders with response letters and quality management related communication with sponsors, IRBs and the FDA.

O. Review and interpret quality reports (audits, inspections, and complaints) and act as a resource to ensure patient safety and data integrity are maintained by site personnel.

P. Lead operational meetings to ensure lessons learned and best practices are shared across all sites and report on quality metrics and trends across all sites.

Q. Review and ensure site compliance with FDA guidance, SOPs, GxPs and Flourish site standards.

R. Create metrics on quality performance and report to senior leadership on overall quality health of the organization, as well as potential areas of risk.

S. Additional duties as assigned by your manager.

Requirements

PHYSICAL REQUIREMENTS AND/OR ENVIRONMENTAL FACTORS:

A. Work is performed remotely.

B. Travel may be required up to 30%.

C. Daily computer use.

D. Occasional evening and weekend work schedules.

MINIMUM REQUIREMENTS:

Education: Master’s degree or equivalent.

Experience: Minimum 8 years’ experience with quality and compliance management in a clinical research environment, strong understanding of research activities and processes at research sites, either hospital or clinic setting; exceptions may apply to extraordinary candidates with clinical operations background and strong quality and compliance mindset.

Knowledge and Skills:

A. Expert working knowledge of clinical research quality management system requirements.

B. Comprehensive knowledge of clinical research processes and research site conduct.

C. Collaborative and supportive team player with ability to lead cross-functional initiatives while fostering relationships between quality and operations.

D. Expert-level understanding of the quality management process, including issue identification, triage, RCA, and CAPA.

E. Expert working knowledge of GCP guidelines and regulations as well as requirements of regulatory documents and submissions to IRBs.

F. Expert in data compliance and the requirements, best practice and organization of a clinical research site.

G. Excellent leadership skills, including mentoring and training of staff members at all levels.

H. Excellent interpersonal skills, including assertiveness, persistence, flexibility, highly organized and detail oriented.

I. Proactive, flexible, and driven mindset, able to keep yourself and others on task.

J. Extremely organized with a high attention to detail.

K. Excellent oral and written communication skills.

L. Excellent computer skills to include Office365 products.

M. Strong problem solving, risk assessment and impact analysis abilities.

N. Ability to think independently and influence when appropriat

Benefits

Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, employee referral program, employee assistance program, life insurance, disability insurance, and a generous PTO plan covering vacation, sick, personal days and 8 paid holidays.

Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.

From $25, paid onceGet the CV for this job

What happens when you press

One press. We do the rest.

  1. A CV for this posting

    Written against Workable (global search)'s own wording, from every piece of relevant proof in your profile.

  2. 25 readers review it

    Recruiter, hiring manager, skeptic and more read every draft, round after round. You get the best round.

    The review screen in CV Rocket: how each CV was read, round by round.
  3. We apply on Workable (global search)'s form

    Our application engine gets through the hardest forms there are. Where a question needs you, AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

    An application in CV Rocket: every answer filled in on the employer's form.
  4. Every reply, sorted

    Workable (global search)'s answer lands in your private mailbox, and we classify it on arrival: interview, question, rejection.

    The CV Rocket inbox: each employer reply classified as an interview, an action or a rejection.
  5. Reply with AI

    AI helps you write the email, checks it and sends it. We show you whether the recruiter read it.

  6. The interview in your calendar

    Full integration with your calendar. The invitation goes straight in.

    An interview invitation in the CV Rocket inbox, added to the candidate's calendar.
Get the CV for this job

From $25 per CV, paid once. No subscription.

Why it works

3×

more interviews than doing it yourself with ChatGPT.

ChatGPT writes a CV and never learns what happened to it. We see every reply. For each CV we know:

  • How it was written, and how the review scored it
  • When we applied, and how long after the posting went up
  • Which posting, which company, which city
  • Who got the interview, and who heard nothing

That is how we know which CVs get called.

Get the CV for this job

From $25 per CV, paid once. No subscription.

The numbers game

More applications. More interviews.

Every application goes out with its own CV, written for that posting and paid once. Send enough of them and the law of large numbers finds you the job.

By hand5–10
With CV Rocket100
applications a day

Nearby

Live postings like this one

Same employer first, then the same role elsewhere.

Before you press

Straight answers

Get the CV for this job

From $25 per CV, paid once. No subscription.

What if my background isn't good enough?

We make the most of the background you have. The CV uses every piece of relevant proof your profile holds, and one of the 25 readers reads your whole profile and flags what the CV left out.

Do you really apply for me?

Yes, on the employer's own form, the hardest ones included. Where a question needs you, you answer it right there and AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

Is it a subscription?

No. You pay once per CV, from $25. Every application goes out with its own CV, written for that posting.

One job. One CV.
Paid once.

Pick the posting you want. We write for it, apply for you and catch the reply.

Get the CV for this job

From $25 per CV, paid once. No subscription.