1,000+ matching jobs for “Clinical Research Associate”

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Thermo Fisher Scientific

Associate Director CTM FSP

Remote, District of Columbia, USA

Pay posted by employer$120,000–$150,000

Join Us as Associate Director CTM – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Thermo Fisher Scientific

Site Payments Associate II - Reconciliation

Remote, Philippines +1 location

… with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and …

Added Nov 4, 2026

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Thermo Fisher Scientific

Site Payments Associate II - Reconciliations

Remote, Bulgaria

Added Oct 16, 2026

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IQVIA Holdings

Associate Director, Biostatistics - Global BIOS

Frankfurt, Hesse, Germany

… resource for the department, ensuring scientific integrity in the application of statistical methodology to clinical trials and assist the Director in strategic planning and resource allocation for the department. You will …

Added Oct 15, 2026

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IQVIA Holdings

Jr. Financial Operations Associate

Buenos Aires, Argentina

… contractual commitments from study initiation through closeout; Maintains the master site list for assigned clinical trials, ensuring that all setup documents have been received – including but not limited to, executed …

Added Oct 15, 2026

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Thermo Fisher Scientific

Associate Contract Specialist

Remote, United Kingdom

… information • Fluency in English required • Ability to manage multiple deadlines • Experience in clinical research, pharmaceutical, or life sciences industry preferred

Added Oct 16, 2026

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Amgen

Associate Director, Biostatistical Programming

India - Hyderabad

Full time
Regular

Associate Director, Biostatistical Programming HOW MIGHT YOU DEFY IMAGINATION? If you feel like you’re part of …

Added Oct 15, 2026

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Thermo Fisher Scientific

Lab Project Associate II

Austin, Texas, United States

Added Oct 16, 2026

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IQVIA Holdings

Associate Medical Director (Nephrology)

Buenos Aires, Argentina

… education. Certification in Nephrology (mandatory) 3 - 5 years of prior relevant experience in general clinical medicine. Previous clinical research experience as an investigator or in the Pharma, CRO, or Biotech …

Added Oct 15, 2026

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IQVIA Holdings

Associate, Market Access Consulting

Mexico City, Mexico +1 location

… and actionable recommendations for clients • Conduct primary (qualitative) and secondary (quantitative) research on markets, payers, physicians, patients, and competitive products to identify key findings for client …

Added Oct 15, 2026

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Johnson & Johnson

Associate Medical Director, Pediatric Development Team

Spring House, Pennsylvania, United States of America

Full time
Regular

… every step of the way. Learn more at https://www.jnj.com/innovative-medicine This position will serve as an Associate Director for Clinical Immunology products in development with indications in pediatric Immunology, …

Added Oct 15, 2026

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IQVIA Holdings

Pre-Analytical Biorepository Associate

Valencia, California, United States

Pay posted by employer$25,300–$74,800

We are seeking a Pre-Analytical Services Associate to join IQVIA Laboratories business in Valencia, CA. We hire passionate innovators who drive healthcare …

Added Oct 15, 2026

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Thermo Fisher Scientific

Business Development Associate

Beijing, Beijing, China

… successful execution of CDA/NDA and process smooth handover to the respective BDMs. · Conduct desk research and market mapping to build and maintain a strong pipeline of prospects. · Support outbound campaigns …

Added Oct 16, 2026

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Regeneron Pharmaceuticals

Automation Associate - Automation Core

TARRYTOWN

Full time
Regular

Pay posted by employer$70,300–$110,100

Automation Associate Automation Core Build our future together: The Automation Core is a centralized high-throughput core …

Added Oct 30, 2026

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IQVIA Holdings

Associate Consultant, Advanced Analytics

São Paulo, Brazil

Essential Functions Business Development Support: Research clients’ business problems and find potential solutions through our offerings, while supporting proposals …

Added Oct 15, 2026

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Thermo Fisher Scientific

Associate Nutrition Specialist / Dietitian

Remote, Texas, USA

… or helping find cures for cancer. DESCRIPTION: Provides nutrition expertise and operational support for clinical trial nutrition programs and services. Supports the design, implementation, and delivery of …

Added Oct 16, 2026

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Amgen

Database Design Sr Associate

India - Hyderabad

Full time
Regular

… within a global cross-functional environment and collaborates with Data Delivery Leads, Biostatistics, Clinical Operations, vendors, and study teams to deliver high-quality database solutions that support clinical trial …

Added Oct 15, 2026

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IQVIA Holdings

Associate Manager, Specimen Management

Valencia, California, United States

Pay posted by employer$58,800–$122,500

The Associate Manager, Specimen Management supervises a team and oversees daily operations to ensure departmental …

Added Oct 15, 2026

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IQVIA Holdings

Associate Manager, Specimen Management

Valencia, California, United States

Pay posted by employer$58,800–$122,500

The Associate Manager, Specimen Management supervises a team and oversees daily operations to ensure departmental …

Added Oct 15, 2026

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Abbott Laboratories

Accounts Payable Associate - (Pipeline)

Philippines - Taguig City

Point-of-care diagnostics is a growing and dynamic industry helping to improve clinical and economic outcomes globally. Abbott brings a variety of expert viewpoints on new innovations, insights, …

Added Oct 15, 2026

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Thermo Fisher Scientific

Associate Director CTM FSP

Remote, District of Columbia, USA

Pay posted by employer$120,000–$150,000

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About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as Associate Director CTM – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As Associate Director CTM, you will manage a team of clinical staff and managers across several countries or a geographic area who are responsible for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time, quality, and cost expectations. You may represent the department in cross-functional initiatives that enhance business objectives.

What You’ll Do:
• Manages staff, which may include interviewing and selection, job description preparation, professional development, goal setting, performance management, coaching and mentoring, employee counseling, and separations. Approves courses of action on salary administration, hiring, corrective action, and terminations. Reviews and approves time records, expense reports, requests for leave, and overtime (if applicable).
• Ensures the timely execution of clinical deliverables with a focus on quality deliverables. Supports staff to develop and drive specific and overall project/program strategies to ensure optimum performance by achievement of annual plans and targets. Holds regular project review meetings with staff to identify potential clinical and financial project risks, ensuring contingency plans and solutions are in place, and appropriate, timely escalations are conducted.
• Liaises with cross functional leaders to drive clinical deliverables.
• Oversees the effective project management of clinical budget, forecasting and resourcing. Ensures maintenance of profitability by ensuring clinical activity is conducted within contract scope, through efficient management and guidance to staff. Interprets and analyses data on complex issues and independently make good business decisions.
• Supports the allocation of staff to projects through global resourcing process and manages escalations for resourcing needs. Evaluates out of scope work and assists with contract modifications as needed. Focuses workload assignments to ensure effective project allocation, optimize collaboration with stakeholders, cultivate talent, and promote staff retention by implementing actions and communications aimed to motivate and engage.
• Manages and conducts induction/orientation programs for all new employees, ensuring their smooth assimilation into the company. Provides ongoing training as needed to ensure staff mastery of systems and procedures.
• Ensures all direct report CVs, training records and experience profiles are complete and up to date.
• Reviews and ensures compliance with SOPs/WPDs/company procedure training and any other subjects that impact on clinical development. May contribute in the development of SOPs and WPDs as needed.
• May participate in cross functional / departmental projects or initiatives as needed.
• Drives a culture of immediate action and proactive escalation including early escalation to present solutions to risk, effective interaction with stakeholders, and effective management of general quality risk. Effectively escalates quality issues, requests QA audits as appropriate, and facilitates client and internal quality assurance audits as required.
• May provide input into bids and contribute to the procurement of new business where required

Education and Experience Requirements:
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 10+ years).
• 5+ years of management responsibility
• Proven leadership skills
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:
• Excellent & effective mentoring/leadership/supervisory skills
• Effective organizational and negotiation skills; effective at multi-tasking
• Superior interpersonal skills and proven ability to be creative in problem solving and conflict resolution
• Capable of utilizing problem-solving techniques applicable to constantly changing environment
• Experienced in motivating, integrating individuals/teams, inducting, coaching and teaching direct reports
• Capable of effectively and proactively managing and coaching employees with performance issues
• Proven record to proactively direct and promote teamwork in a multi-disciplinary and/or multi-cultural team setting
• Expert knowledge of clinical trials in releveance to regulations and guidelines e.g. ICH/GCP, FDA guidelines, etc
• Excellent ability to evaluate medical research data, demonstrate proficient knowledge of medical terminology and therapeutic areas
• Proficient knowledge with company practice and processes to provide guidance and direction
• Proficient in using company tools to ensure oversight of financial management of projects for direct reports as well other tools needed to manage the timelines and quality of the data
• Strong attention to detail
• Competent use of computer and company systems to manage performance
• Strong attention to detail, ability to synthesisze and communicate complex information
• Strong knowledge of English language & grammar with effective written and oral communication skills

Working Conditions and Environment:
• Work is performed in an office environment with exposure to electrical office equipment.
• Occasional drives to site locations, frequent travels both domestic and international.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.

Compensation and Benefits

The salary pay range estimated for this position Trial management Sr Manager based in District of Columbia is $120,000.00–$150,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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