Clinical Trials Manager Job at Connexion Systems & Engineering, Inc (Durham)

Sr. Manager / Manager – Clinical Trials (Coverage Analysis / Calendar Build / Budgeting)

This role requires a manager with 8+ years of experience in clinical trials, inc...

Location

India , Pune

Salary:

Not provided

Suma Soft Pvt Ltd

Expiration Date

Until further notice

Requirements

Graduation in Life Science/Pharmacy preferred
Domain Experience – 8+ Years
Managerial Experience – 2+ Years
Excellent communication and interpersonal skills

Job Responsibility

Managing complex trial finances
Leading a team

Fulltime

Clinical Trial Manager/ Sr Clinical Trial Manager (PM/ Sr PM)

Clinical Operations Lead - Early Development Oncology. ICON plc is a world-leadi...

Location

United States , Raleigh, Blue Bell

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

BS/BA degree or a relevant degree with strong emphasis on science, or equivalent experience
Minimum of five years of relevant experience in the biopharmaceutical industry or other relevant clinical research experience, with a focus on skills and competencies
Must have working knowledge of ICH Good Clinical Practices and other relevant regulatory/health
Prior experience in assisting the conduct and management of multinational clinical trials is preferred
Ability to effectively manage multiple priorities across several protocols and therapeutic areas simultaneously
Experience in oncology studies required (phase I preferred)

Job Responsibility

Participate as a member of a working group and perform special projects, as assigned, to improve the efficiency, effective and quality of the functioning of the Development Operations department
Act as preliminary liaison for study sites to convey study information, answer questions and in accordance with the escalation pathway
Develop relationships with investigational sites, HCPs, and institutions to enhance conduct of the trial
Monitor study-specific timelines and key deliverables
focus on management of all relevant external vendors (e.g., Monitoring, Sample management, IVRS, Laboratory, etc)
Participate as a member of the multi-disciplinary trial(s) team
Participate in coordinating efforts with internal Pharmacovigilance, and safety group as needed
Participate in data review and discrepancy resolution as needed
Assist in the development of the IP and co-medication strategy (quantities, labels, depots, tracking, etc.) working closely with other departments
Plan and organize meetings with team support (e.g., investigator/coordinator meetings, DMC, SMC, safety call, etc.) as appropriate

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Senior Sales Manager- Clinical Trials

This role is in support of Alcura, a business offering clinical trial supply and...

Location

United States , Columbus; Remote

Salary:

88700.00 - 126940.00 USD / Year

Cencora

Expiration Date

Until further notice

Requirements

Bachelor’s degree or equivalent preferable, but career experience considered
Minimum 8 years of experience in business development and global customer relationship management, with a focus on the clinical trials sector
Proven track record of managing senior-level client relationships and driving revenue growth
Experience working with CROs, pharmaceutical and biotech companies in an international context
Familiarity with clinical supply logistics is a plus
Established network of decision-makers in the clinical trials sector, including CROs, pharmaceutical and biotech companies
Strong presenting and selling capabilities, with the ability to simplify complex concepts for diverse audiences
Excellent communication and presentation skills, with the ability to engage confidently with senior executives (C-Suite) and adapt to various cultural and organizational contexts
Self-motivated and tenacious, capable of working independently
High level of professional gravitas, diplomacy, and negotiation skills to build trust with clients and internal teams

Job Responsibility

Leverage an existing network of contacts and decision-makers in the clinical trials sector to generate new business opportunities
Promote US-based clinical trial services, including Packaging, Labelling, Storage, and Distribution (PLSD), Comparator medications, and ancillary sourcing
Develop and execute a strategic sales plan to establish presence in the US market, targeting CROs, pharmaceutical and biotech companies
Build and maintain strong relationships with senior-level stakeholders (C-Suite) to influence commercial opportunities and decision-making
Confidently present services and value proposition, demonstrating professional gravitas in all client interactions
Serve as the primary point of contact for US clients, ensuring seamless communication across global teams
Manage the entire sales cycle, from prospecting and lead generation to closing deals, while maintaining strong customer relationships
Lead client meetings, sales pitches, and quarterly business reviews, preparing agendas and consolidating input from internal teams
Work closely with sales peers and teams across Europe
Collaborate with commercial teams across affiliates to provide a comprehensive customer approach

What we offer

medical
dental
vision care
comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness
support for working families
backup dependent care
adoption assistance
infertility coverage
family building support
behavioral health solutions

Fulltime

Senior Product Manager (Pharma Clinical Trials)

Pur Pharma Solutions business is looking for an experienced product manager to p...

Location

United Kingdom , Oxford

Salary:

65000.00 - 75000.00 GBP / Year

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Bachelor's degree in business, marketing, life sciences, or a related field
Proven experience in product management within healthcare, pharma, or medical devices
Demonstrated success launching and managing innovative medical technology products
Strong understanding of the pharmaceutical landscape, including regulatory and market dynamics
Excellent analytical and problem-solving skills, with the ability to turn insights into action
Strong communication and presentation skills across technical and non-technical audiences
Experience with product development methodologies and tools
Highly collaborative, with the ability to influence cross-functional teams
Strategic mindset with a focus on innovation and differentiation
Strong leadership and stakeholder management skills

Job Responsibility

Define and lead technical and commercial product strategy
Own and manage the product roadmap, aligning stakeholders across the business
Drive product lifecycle activities from concept through commercialisation
Act as a product expert in pre-sales, RFPs, and client engagements
Gather and translate customer insights into product improvements and innovation
Monitor market trends, competitor activity, and emerging opportunities
Collaborate with engineering, QA, regulatory, and operations to ensure compliance and quality
Support business development by building and maintaining a strong commercial pipeline
Represent Perspectum at conferences, events, and industry forums
Lead marketing initiatives aligned to your product portfolio

Fulltime

Supply & Logistics Project Manager in Clinical Trials

Are you ready to lead impactful projects ensuring secure, timely patient treatme...

Location

Poland , Warsaw

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Strong understanding of GxP regulatory framework
Extensive pharmaceutical/clinical research/biotech industry experience
Proven expertise in laboratory and/or clinical trial supply chain management
Excellent project management and operational leadership skills
Client-focused approach with strong business acumen
Financial management and negotiation abilities
Team mentorship and stakeholder management skills
Bachelor's degree in biology, pharmacy, health sciences, business administration, or equivalent experience
Fluent English (written and spoken)

Job Responsibility

Develop and execute supply strategies for IMP/NIMP, ANS, and laboratory samples
Ensure GLP, GDP, GMP compliance across all participating countries
Manage project timelines, budgets, and operational resources
Oversee third-party providers and negotiate contracts
Conduct risk assessments and develop mitigation plans
Serve as regulatory point of contact and resolve client issues
Lead process improvements and system optimization

What we offer

Benefits vary by country, but Parexel is passionate about our team’s overall wellness
Career Advancement
Talent Community

Fulltime

New

Clinical Project Manager - Early Phase Trials

As a part of the global Project Leadership group at Parexel, you are responsible...

Location

United States , Remote

Salary:

125000.00 - 138000.00 USD / Year

Parexel

Expiration Date

Until further notice

Requirements

2 years of Project Management experience with Parexel or 3 to 5 years in related fields
Experience as a Functional Team Leader or in coordinating clinical trials
Knowledge of ICH-GCP and pharmaceutical industry regulations
Proficiency in MS-Office products
Bachelor’s degree in a science-related field or equivalent work experience

Job Responsibility

Lead cross-functional teams to deliver high-quality and patient-focused clinical trials
Collaborate with clients and internal stakeholders to identify project requirements, develop project plans, and manage project timelines and budgets
Manage the financial aspects of projects, including revenue recognition, milestone payments, and monthly pass-through invoices
Own the sponsor relationship and manage sponsor communication
Serve as the central point of contact and escalation for functional teams
Proactively communicate project progress, risks, and solutions to sponsors and internal teams
Lead regular meetings with sponsors and project teams to ensure objectives are met
Review relevant materials and attend strategy meetings
Prepare for Bid Defense and develop project management strategies
Attend Bid Defense and handover meetings

What we offer

Annual performance-based bonus plan
Annual salary review
Additional total rewards incentives
Paid time off
401k match
Life insurance
Health insurance
Other benefit offerings in accordance with the terms of applicable plans

Fulltime

Senior Manager, Clinical Operations/ Senior Global Trial Manager - FSP

Parexel are currently recruiting for an experienced Global Study Operations Mana...

Location

Italy; United Kingdom , Remote; Remote

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Minimum of 7 years of relevant clinical trial management experience
Global trial management experience is essential
Experience managing CRO outsourced studies is essential
Excellent leadership, communication, and organizational skills
Able to multi-task under limited direction and on own initiative
M.S/M.A/Ph.D or B.A/B.S/nursing degree is essential
Prior and demonstrable experience working at a senior level within Study start up preferred

Job Responsibility

Accountable for the end-to-end clinical trial delivery
Providing operational leadership and oversight of cross-functional deliverables
Leading a cross functional trial team to build and deliver the trial operational plan
Responsible for leading the Cross functional trial team to influence and execute delivery of the operational plan and for end-to-end trial execution
Accountable for overall trial delivery, budget, timelines, quality, and milestones
Oversight of all aspects of CRO/vendor identification, set up, statement of work creation, budget oversight and performance (KPI’s and metrics)
Proactively ensure that trial deliverables and milestones are met according to corporate and study-level goals
Identify risks and ensure mitigations and contingencies are being initiated and followed through
Ensure trial Is operationalized in compliance with global health authority regulations and guidelines and internal operating procedures and processes
Participate in preparation for, and conduct of, Health Authority Inspections and internal QA audits

Clinical Research Budgeting Analyst - Clinical Trials

The Clinical Research Budgets Analyst plays a critical role in supporting sponso...

Location

United States , Seattle

Salary:

39.45 - 61.24 USD / Hour

Providence Swedish

Expiration Date

Until further notice

Requirements

Bachelor's Degree or 4 additional years of related experience
6 years of direct experience in budget development, preferably in clinical trial or medical setting

Job Responsibility

Prepare and maintain accurate budget templates for sponsored clinical trials
Conduct comparative reviews of budgets offered by study sponsors
Set up study payment milestones in the Clinical Trial Management System
Review New Study routing forms and essential study start‑up documents
Perform itemized cost analyses and interpret clinical protocols to develop budget milestones
Provide accurate patient cost descriptions for the Informed Consent Form (ICF) to be submitted to the IRB
Update budgets, milestones, and ICF information as needed to reflect contract or protocol amendments
Work closely with the coverage analysis team, contract analysts, regulatory team, program managers, and internal finance groups
Manage high‑volume workflow across multiple research programs, each with unique processes and requirements

What we offer

retirement 401(k) Savings Plan with employer matching
health care benefits (medical, dental, vision)
life insurance
disability insurance
time off benefits (paid parental leave, vacations, holidays, health issues)
voluntary benefits
well-being resources

Fulltime

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Clinical Trials Manager

Job Description

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