ZipRecruiter

Log In

1

Tki Jobs (NOW HIRING)

Tessenderlo Kerley, Inc.

HSE Specialist

Phoenix, AZ

As a Health Safety Environmental (HSE) Specialist at Tessenderlo Kerley, you will be responsible for supporting HSE programs for a portion of TKI's 19 chemical manufacturing plants, laboratories ...

Tessenderlo Group

Logistics Coordinator

Phoenix, AZ · On-site

$19.25 - $25.75/hr

Investigate various complaints and inquiries in order to arrive at a satisfactory result for TKI Customers. * Partner with 3rd party carriers/dispatchers to ensure all DOT regulations are followed ...

Tessenderlo Group

HSE Specialist

Phoenix, AZ · On-site

As a Health Safety Environmental (HSE) Specialist at Tessenderlo Kerley, you will be responsible for supporting HSE programs for a portion of TKI's 19 chemical manufacturing plants, laboratories ...

Tessenderlo Kerley, Inc.

Logistics Coordinator

Phoenix, AZ

$19.25 - $25.75/hr

Investigate various complaints and inquiries in order to arrive at a satisfactory result for TKI Customers. * * Partner with 3rd party carriers/dispatchers to ensure all DOT regulations are followed ...

TKI Designs Inc

Jewelry Style Advisor

Astoria, NY

$40K - $50K/yr

We are seeking a Jewelry Sales to become an integral part of our team! You will be responsible for selling products, merchandise, and services in a retail setting in order to drive company revenue.

previous page

Showing results 41-60

All JobsTki Jobs

Tki information

See salary details

$12

$18

$25

How much do tki jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for tki in the United States is $18.36, according to ZipRecruiter salary data. Most workers in this role earn between $15.38 and $20.67 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Tki?

I'm sorry, but 'Tki' does not appear to be a recognized professional occupation, so I cannot provide a relevant answer.

What is a Tki?

TKIs, or Tyrosine Kinase Inhibitors, are a class of targeted cancer therapy drugs that block the action of enzymes called tyrosine kinases. These enzymes play a key role in the signaling pathways that control cell growth and division. By inhibiting these enzymes, TKIs can help stop the growth of cancer cells, making them a common treatment for certain types of cancers, such as chronic myeloid leukemia (CML) and some lung cancers. TKIs are usually administered orally and may have different side effects depending on the specific medication and patient.

What are some common challenges Tki professionals face when working on cross-functional teams?

TKI professionals often collaborate with colleagues from diverse disciplines, which can lead to challenges in aligning goals, terminology, and expectations. Navigating these differences requires strong communication skills and the ability to translate technical concepts for non-specialists. Building trust and fostering a culture of open feedback are key to overcoming these hurdles and ensuring successful project outcomes. Regular team meetings and clear documentation can also help maintain alignment and minimize misunderstandings.
More about Tki jobs
What job categories do people searching Tki jobs look for? The top searched job categories for Tki jobs are:
Tki jobs near you
Infographic showing various Tki job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $38,189 per year, or $18.4 per hour.

Associate Director, Clinical Operations

Summit Therapeutics

Princeton, NJ • On-site

Full-time

Posted 8 days ago

Job description

About Summit:
Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit's core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence.
Summit's team is inspired to touch and help change lives through Summit's clinical studies in the field of oncology. Summit has multiple global Phase 3 clinical studies, including:
Non-small Cell Lung Cancer (NSCLC)
  • HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI.
  • HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC.
  • HARMONi-7: Phase 3 clinical study which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC.

Colorectal Cancer (CRC)
  • HARMONi-GI3: Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy.

Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China's National Medical Products Administration (NMPA). Summit is headquartered in Miami, Florida, and has additional offices in California, New Jersey, the UK, and Ireland.
ASSOCIATE DIRECTOR, CLINICAL OPERATIONS
Overview of Role:
The Associate Director, Clinical Operations provides operational leadership for clinical trial execution, overseeing the clinical operations team and vendor performance. This role ensures effective study delivery through cross functional collaboration, proactive risk management, and strong execution oversight. This role leads vendor strategy and oversight ensuring external partners deliver against scope, timelines, quality expectations, and operational objectives.
The ideal candidate thrives in a fast-paced, entrepreneurial environment, demonstrates exceptional operational leadership, and possesses strong business acumen with an understanding of the competitive landscape, capital allocation, and value creation throughout drug development.
Role and Responsibilities:
  • Oversees the clinical operational strategy, planning, and execution of one or more global clinical trials.
  • Ensures internal clinical and external teams deliver on time, within budget and in compliance with GCP, ICH guidelines, applicable regulations and are always inspection-ready.
  • Drafts, reviews and approves internal and external study-related plans, processes, and documents including Informed Consent Forms, Investigator Agreements (CTA), CRFs, CRF Guidelines, statistical/pharmacokinetic analysis plans, monitoring plans, data management plans, and safety monitoring activities.
  • Manages CROs, vendors, and strategic partners through robust governance, performance metrics, and risk management.
  • Identifies operational risks early and implement proactive mitigation strategies escalating to leadership.
  • Drives financial accountability through effective budget management and resource utilization.
  • Oversees maintenance, quality, and completeness of the Trial Master File (TMF) and ensures all TMF quality reviews are completed.
  • Manages CRO proposals, vendor contracts/change orders, and outsourcing strategies ensuring delivery with a focus on value and return on investment.
  • Partners with Finance to provide oversight of vendors costs, supporting prudent operational decisions that align with budgets and financial plans.
  • Oversees preparations for regulatory inspections, supports inspection management activities, and ensures the project is always inspection-ready.

  • Manages, mentors and provides guidance to CTMs, CRAs, and other Clinical Operations team members.
  • Drives continuous improvement initiatives and contributes to development of Clinical Operations processes and standards.
  • Represents Clinical Operations on cross-functional study teams and governance meetings.
  • Fosters collaboration with external partners, Regulatory Affairs, Clinical Science, Data Management, Biostatistics, Pharmacovigilance, Quality Assurance, CMC, and Commercial teams.
  • All other duties as assigned

Experience, Education and Specialized Knowledge and Skills:
  • Bachelor's degree or equivalent in life science, nursing, pharmacy, medical laboratory technology, or other health/medical-related areas
  • 10+ years of direct clinical trial management experience overseeing phase II/III international oncology clinical trials
  • Ability to travel internationally to visit clinical sites and study meetings. Amount will vary upon project needs (up to 20%)

Preferred Experience, Education and Specialized Knowledge and Skills:
  • Consistently demonstrates ability to solve problems and use clear judgment in relation to regulatory requirements, interactions with external parties, timelines, and complex clinical programs
  • Excellent planning, leadership, communication, negotiation, and organizational skills when working with both internal and external teams.
  • Expert knowledge of the drug development process, ICH guidelines/GCP with a deep understanding of all phases of clinical trial execution and the ability to apply this knowledge to complex, global studies.

This is the pay for this position
Pay Transparency
$174,000-$205,000 USD
Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. The total compensation package for this position may also include bonus, stock, benefits and/or other applicable variable compensation.
Summit does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Summit's Talent Acquisition team at recruiting@smmttx.com to obtain prior written authorization before referring any candidates to Summit.
Summit Therapeutics Inc. is an Equal Opportunity Employer and takes pride in creating and maintaining diverse environment. We do not discriminate in recruitment, hiring, training or promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.

Apply