CrawlJobs Logo

Site Contracts Associate I - FSP

· Job Posted June 14, 2026
Apply Position
Job Link Share

Job Description

The Site Contract Associate I (“SCA”) is responsible for negotiation with sites, finalization, and execution of all types of site contracts required for site activation. SCA is also responsible for ancillary documents associated to site contracts. Post site activation, SCA is responsible for negotiation, finalization, and execution of any amendments to the original contracts. The SCA ensures the highest standard of quality of final documents, as well as their compliance with relevant regulatory requirements, guidelines, and respective country’s applicable laws. The SCA ensures that contracts meet needs of both clients and clinical trial sites, protecting best interests of clients and the company (as applicable), while nurturing and maintaining positive relationships with clinical trial sites.

Job Responsibility

  • Draft, review and negotiate all site agreements including but not limited to clinical study agreements, service agreements, team member agreements and other types of related documents like letters, notices, etc
  • Provide context to comments received from sites in light of local legal and business framework, common practices, and past negotiation experience for the purpose of further review up the decisioning chain
  • Apply and scrutinize site contract and related documents and their revisions against negotiation and budget parameters (as applicable)
  • Ensure final documents comply with applicable laws, regulations, and guidelines, including ICH – GCP
  • Ensure the best interest of both clients and Parexel are met
  • Serves as key communication liaison between site contracts staff and internal and external customers
  • Manage the contract execution process, including obtaining required signatures and ensuring timely execution of the document by all parties
  • Follow record maintenance and archival guidelines to ensure they are met
  • Develop and maintain positive relationships with clinical trial sites
  • Develop and maintain a thorough understanding of the clinical trial protocol, budget, and timelines to ensure that contract terms align with the overall trial goals and objectives
  • Identify potential issues or concerns with contract terms and collaborate with internal stakeholders and clinical trial sites to find mutually acceptable solutions
  • Stay up to date with relevant regulatory requirements, guidelines and applicable laws in respective country
  • Identifies if all necessary documents, such as Power of Attorney, Insurance Certificates, Indemnification Letters, Informed Consent Form, referenced agreements or any other correlated documents are in line and in place for the need of Clinical Site Agreement
  • Track and report on the statuses of site contracting activities to Site Contract Lead, other internal stakeholders and study teams
  • SCA is responsible for first time quality by self-check and reviews contracts for completeness and accuracy
  • Ensures that changes are appropriately made, approved and documented
  • Works within the forecasted country/site contracting timelines, ensures they are complied with and tracks milestone progress in agreed upon contract tracking system in real time
  • Identifies possible contract or process operational risk and proactively works with SCL to provide solutions
  • Reviews and complies with Standard Operating Procedures (SOPs) any other relevant applicable guidance in a timely manner, keeps training records updated accordingly and ensures timesheet compliance
  • Ensure adequacy and accuracy of archived records
  • Identify and implement process improvements to increase efficiency and quality in the site contracting process
  • Provide guidance and support to study teams and project management on site contracting matters in the respective country
  • Participate in cross-functional communication to identify process improvements and contribute to the development of site contracting strategies

Requirements

  • 1-4 years of experience in site contracting or combination with a related field within the CRO industry
  • Bachelor's degree in a related field (e.g., law, economics, business, social sciences), equivalent training or industry experience
  • Solid working proficiency of all MS Office Products specifically, Excel, Word, and PowerPoint
  • Possess strong negotiation, diplomacy, and excellent organizational skills with demonstrated experience handling multiple projects
  • Excellent interpersonal, verbal and written communication skills
  • Strong problem-solving skills
  • Ability to successfully work in a 'virtual' team environment
  • Must have strong analytical skills with the ability to create or interpret legal language and budgets
  • Maintain grace under pressure while displaying a high level of professionalism
  • Align internal and external resources to achieve objectives
  • Attention to detail
  • Comprehend and interpret contract language
  • Identify problems independently and execute solutions
  • Quickly comprehend desired end-result, goal or objective and act to accomplish
  • Polished presentation skills
  • Quality-driven in all managed activities
  • Fluent in written and spoken English

Nice to have

Command of additional languages is beneficial

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Similar Jobs for

Site Contracts Associate I - FSP

8 matching positions

Gco Associate I - Fsp

Location
Location
United Kingdom
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BS/BA or bachelor's degree in life sciences or a related discipline is an asset
  • 2-5 years of relevant experience in clinical trial support, site activation, or clinical operations (pharmaceutical company or CRO preferred)
  • Exposure to country or site-level clinical trial operations and supporting documentation workflows
  • Experience supporting contracting, regulatory, or vendor-related documentation processes is an advantage
Job Responsibility
Job Responsibility
  • Execute operational tasks across start-up, conduct and close-out phases
  • Maintain and update trackers, timelines, or task status to support visibility of progress and risks
  • Assist with follow-up on outstanding country or site deliverables and escalate gaps or delays to responsible leads as required
  • Could support coordination with local vendors and CROs by tracking deliverables and ensuring required documentation is received and filed
  • Undertake periodic review of study and site files for completeness and assist with reconciliation activities
  • Maintain site-facing communications, as applicable, to complete assigned work activities
  • Demonstrate a proactive approach to ongoing improvement by consistently seeking opportunities to enhance processes and optimise workflows
  • Interactions with sites for collection of documentation needed for Institutional Review Board (IRB), Local Ethics Committee (LEC), Regulatory Authority (RA) submission and Investigator Initiation Packages (IIP) Updates preparation as per country requirements
  • Responsible for preparation of Institutional Review Board (IRB)/Local Ethics Committee (LEC) clinical trial applications by pre-populating documents, locating required records from systems (e.g., PTMF), and supporting processing through approval steps
  • Submission to local Regulatory Agency where required
  • Fulltime
Read More
Arrow Right

Senior Clinical Trial Manager

Sr Local Trial Manager – Solid Tumor Oncology - Home Based (US) ICON plc is a wo...
Location
Location
United States , Blue Bell
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BA/BS degree
  • Degree in a health or science related field
  • 3 - 5+ years of trial end to end management experience
  • Solid Tumor Oncology experience required
  • Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures
  • Strong IT skills in appropriate software and company systems
  • Proficient in speaking and writing the country language and English. Good written and oral communication skills as appropriate
  • To qualify, applicants must be legally authorized to work in the United States and should not require, now or in the future, sponsorship for employment visa status
Job Responsibility
Job Responsibility
  • Serves as the primary point of communication for sites, facilitating internal client teaming to drive issue resolution
  • Intimately understands site operational model and owns relationships with critical site stakeholders to provide a voice for the site to the client's teams
  • Contribute to quality Site Selection through participation in site feasibility ensuring consistent conduct of site qualification visits and appropriate follow-up of site qualification visit report and country feasibility report
  • Collaborates with central study team and local stakeholders as applicable for final selection of sites to participate in trial
  • Ensures local/country team is meeting recruitment targets with high quality data on time and within study budget by providing input to study level documents and leading/coordinating local team activities in compliance with SOPs, other procedural documents and applicable regulations
  • Act as primary company contact for assigned trial sites, engaging with Investigator and Site Staff throughout the life of the trial
  • Focuses on investigator engagement through timely follow up with sites
  • Promptly communicates relevant status information and issues to appropriate stakeholders
  • Drive study compliance by maintaining and updating trial management systems, using study tools and management reports available to analyze trial progress
  • When necessary initiates corrective and preventive actions (CAPA) when the trial deviates from plans and communicates study progress and issues to study management teams and Quality & Compliance team
What we offer
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
  • Fulltime
Read More
Arrow Right

Start Up Project Manager II- FSP

The Start Up Project Manager is responsible for defining, developing and deliver...
Location
Location
Canada
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Demonstrated clinical research experience
  • Demonstrated start up experience
  • Demonstrated project management experience
  • Global start up experience (Exposure across a minimum of North America, Asia and Europe) across multiple therapeutic areas
  • Concurrent management of complex processes within and across countries in multiple regions of the world
  • Technical expertise in the use of software for the management of clinical studies (enterprise project management, off the shelf and custom built) including reporting systems (dashboards with associated medium to complex data analysis)
  • Expert ability to comprehend status and adapt communications across a diverse audience
  • Perform critical path analysis across multiple related project plans, will use key performance indicators to assist in driving overall delivery to operational plan across roles
  • Will use generative artificial intelligence techniques in daily work
  • Uses risk management techniques as standard to identify and mitigate key project delivery risks
Job Responsibility
Job Responsibility
  • Partner with country / site feasibility specialists to incorporate up to date intelligence for the planned countries and sites into the overall start up strategy and site activation plan, most typically on studies with a medium to large country and site footprint
  • Partner and co-ordinate across teams responsible for regulatory submissions (local and country) and start up functions (e.g. site essential document collection, site contracts and budgets) to align country and site activities, will have ability to form a robust startup strategy and site activation plan for operationally complex studies
  • The SUPM is responsible for delivering site activations to plan, for the SUPM II this will generally be for studies with higher operational complexity (based on a combination of factors such study design, country and site footprint and the priority of the study)
  • As part of the responsibility of delivering site activations to plan the SUPM will co-ordinate with many different roles working at the study and country level to oversee progress of the study specific (e.g. Vendor set-up, investigational product supply etc.) or country specific tasks (e.g. Regulatory submissions, importer of record for supplies etc.) that need to be completed in order for site activations in turn to complete
  • Provide project management of activities directly required to complete all site activations for an assigned study as part of a study management led team to complete all start up activities for a study
  • Lead start up meetings that facilitate alignment of site selection to activation activities performed by country level start up roles with the endorsed trial optimization plan (by senior leadership)
  • The SUPM will work with country level start up roles to seek opportunities to accelerate site activations for their study
  • Accountable for quality and completeness of start up timeline plans at study, country and site level within an enterprise project management (EPM) system
  • Responsible for creating and overseeing the initial baseline and subsequent snapshots of timeline planning within the EPM system
  • In conjunction with study management roles is responsible for ensuring consistent participant compensation for sites and institutions taking part in multiple studies concurrently to eliminate knock-on impact across studies
Read More
Arrow Right
New

Children Law Solicitor/Legal Executive

The successful candidate must be qualified and have experience in Children Law. ...
Location
Location
United Kingdom , Lincoln
Salary
Salary:
Not provided
jobs.360resourcing.co.uk Logo
360 Resourcing Solutions
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Qualified and have experience in Children Law
  • Present a professional image at all times
  • Be well presented, confident and have first class communication skills
  • Hard working, highly organised and able to work to tight deadlines
  • Advising and representing clients in areas of Private Children Law and domestic abuse
  • Conducting advocacy in and out of court
  • Managing files using the Proclaim Case Management System
  • Assisting other members of the Children Department when required
  • Networking and creating and maintaining professional relationships
  • Experience within a Children Law Department
Job Responsibility
Job Responsibility
  • Advising and representing clients in areas of Private Children Law and domestic abuse
  • Conducting advocacy in and out of court
  • Managing files using the Proclaim Case Management System (training will be provided)
  • Assisting other members of the Children Department when required
  • Networking and creating and maintaining professional relationships
What we offer
What we offer
  • Highly competitive salary
  • Bonus Scheme
  • Minimum of 25 days annual leave plus bank holidays
  • Staff discount
  • Wellbeing culture including access to paid for counselling sessions
  • Annual Holiday Sale/Purchase scheme
  • Benefit platform membership
  • Life Assurance
  • Flexible working options
  • Volunteering days
  • Fulltime
Read More
Arrow Right
New

Building Inspector

Come join our dynamic team! The city of Newton is seeking qualified and experien...
Location
Location
United States , Newton
Salary
Salary:
74913.00 - 100477.00 USD / Year
mma.org Logo
Massachusetts Municipal Association
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Experience enforcing building, zoning, or related codes
  • Knowledge of 780CMR MA State Building Code
  • Knowledge of municipal zoning codes and local government regulations
  • Ability to conduct site inspections
  • Relevant certifications or qualifications as required by the City of Newton
Job Responsibility
Job Responsibility
  • Enforce the 780CMR MA State Building Code
  • Enforce the city of Newton Zoning Code and local government building, zoning, occupancy, safety, fire, maintenance codes
  • Conduct building and facility site inspections for conformance to and violations of regulations
  • Perform all other duties as directed
What we offer
What we offer
  • Yearly step increases
  • Excellent benefits
  • Fulltime
Read More
Arrow Right
New

Cost Accountant

We are looking for a Cost Accountant to support financial operations for a manuf...
Location
Location
United States , Ottawa
Salary
Salary:
Not provided
https://www.roberthalf.com Logo
Robert Half
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • At least 1 year of experience in cost accounting or a related accounting role
  • Background in manufacturing accounting with an understanding of production cost flow and inventory valuation
  • Working knowledge of standard costing principles and cost analysis methodologies
  • Ability to interpret financial data, investigate variances, and communicate findings clearly
  • Strong Excel and analytical skills with close attention to accuracy and detail
  • Comfortable working collaboratively with cross-functional teams in a detail-oriented environment
Job Responsibility
Job Responsibility
  • Analyze production expenses, material usage, and labor costs to provide accurate cost data for business decisions
  • Maintain and review standard costing information to help ensure inventory and product costing remain current and reliable
  • Prepare regular cost reports and variance analyses, identifying trends and explaining significant differences from expectations
  • Partner with operations, finance, and other internal teams to support budgeting, forecasting, and margin improvement efforts
  • Assist with inventory valuation, reconciliations, and month-end close activities related to manufacturing accounting
  • Evaluate cost drivers within the production environment and recommend practical opportunities for greater efficiency and control
  • Support financial reporting by ensuring manufacturing-related transactions are recorded accurately and in a timely manner
What we offer
What we offer
  • medical
  • vision
  • dental
  • life and disability insurance
  • 401(k) plan
  • Fulltime
Read More
Arrow Right
New

Pentester

Our client is looking for a skilled security practitioner to steer comprehensive...
Location
Location
Malaysia , Kuala Lumpur
Salary
Salary:
6000.00 - 11000.00 RM / Month
https://www.randstad.com Logo
Randstad
Expiration Date
August 09, 2026
Flip Icon
Requirements
Requirements
  • Penetration Tester with OSCP, CREST CRT required
  • Hold an industry-recognized certification such as OSCP, CREST CRT, or an equivalent credential
  • Possess strong hands-on expertise in penetration testing, alongside web and mobile application security
  • Demonstrate expert knowledge of common exploitation techniques and various vulnerability analysis tools
  • Utilize established attack methodologies like MITRE ATT&CK for thorough and accurate security testing
Job Responsibility
Job Responsibility
  • Take charge of advanced offensive security operations and penetration testing
  • Accelerate career growth with dynamic roles spanning from junior to team lead
  • Strategic Scoping: Plan and manage security assessments across network, web, mobile, and cloud architectures
  • Advanced Testing: Execute realistic red team exercises and offensive security operations to challenge defensive capabilities
  • Actionable Reporting: Document findings clearly to deliver prioritized, actionable recommendations for risk mitigation
  • Client Collaboration: Partner with clients to define testing parameters and translate technical findings into business risks
  • Team Leadership: Mentor junior consultants in penetration testing methodologies, application security, and effective reporting
  • Fulltime
Read More
Arrow Right
New

Cleaner

We're currently recruiting a dedicated Cleaner (Zero Hours) to help ensure the s...
Location
Location
United Kingdom , Wyton
Salary
Salary:
12.76 GBP / Hour
14forty.co.uk Logo
14forty
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Have an enthusiastic can-do attitude
  • Display passion for delivering excellent customer service
  • Be an excellent team player
  • Arrive equipped with a desire to succeed in your role
  • Thrive working under pressure
  • Demonstrate outstanding timekeeping and reliability
  • Have a safety-first mind set
  • Have experience within a similar catering-related role, but this isn't essential.
Job Responsibility
Job Responsibility
  • Representing Defence and maintaining a positive brand image
  • Handling cash and operating the cash register
  • Complying with Food Handling & Hygiene standards
  • Complying with Health & Safety regulations
  • Parttime
Read More
Arrow Right