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Site Activation Manager I

3+ years
$60,930- $115,100
10 April 22, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Site Activation Manager I

Updated:

April 17, 2025

Location:

North America - United States

Job ID:

25002846

About Syneos Health:

Syneos Health® is a leading, fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs, and commercial insights into actionable outcomes that address modern market realities.
Our Clinical Development model places the customer and the patient at the center of everything we do. We continuously simplify and streamline processes to make Syneos Health easier to work with—and to work for.
Discover what our 29,000 employees across 110 countries already know: Work Here Matters Everywhere.

Why Join Syneos Health:

  • Career development and progression opportunities.

  • Supportive and engaged line management.

  • Technical and therapeutic area training.

  • Peer recognition and total rewards program.

  • Total Self culture promoting authenticity, diversity, and belonging.

  • A collaborative, agile, and innovative environment passionate about changing lives.

Job Responsibilities:

  • Collaborate with Business Development, Alliance Management, Contracts and Proposals Development, SSU Country Managers, Project Management, Clinical, Data Management, and Medical Writing.

  • Identify and evaluate issues related to Site Start-Up, regulatory pathways, and patient enrollment; interpret data on complex issues to make sound business decisions and ensure implementation of solutions.

  • Ensure all project deliverables meet internal and customer expectations by providing accurate projections, reports, updates, and ongoing risk management.

  • Develop and maintain strong customer relationships aligned with assigned projects.

  • Oversee all project start-up deliverables, including regulatory maintenance activities, communication with competent authorities, and management of clinical trial agreements and budgets.

  • Maintain timelines following site activation and realign plans when amendments are needed.

  • Update project plans per Standard Operating Procedures and sponsor-scoped processes while ensuring compliance with controlled document requirements.

  • Develop and manage integrated timelines and weekly progress reports, addressing potential risks and gaps.

  • Prepare and present overall SSU strategies and status at client meetings, communicating outcomes to project teams.

  • Review and manage project SSU budgets, ensuring project profitability and implementing corrective measures when necessary.

  • Use professional tools for managing scope, timelines, and resources while ensuring effective budget management.

  • Notify appropriate teams of out-of-scope work and track it accordingly.

  • Prepare core submission documents and regulatory impact assessments for amendments.

  • Collaborate with Project Managers and Medical Departments for Subject Information Sheet/Informed Consent Form updates.

  • Oversee collation, quality review, and submission of country-specific applications.

  • Contribute to departmental change initiatives and process improvements.

Qualifications:

  • Bachelor’s Degree required; Higher Degree preferred.

  • Excellent understanding of clinical trial processes across Phases II-IV and ICH GCP guidelines.

  • Strong knowledge of clinical trial protocols, specifications, and start-up processes.

  • Project management experience in a fast-paced environment.

  • Good vendor management and organizational skills with the ability to manage multiple projects.

  • Excellent communication, presentation, and interpersonal skills.

  • Quality-driven with strong problem-solving and negotiating abilities.

  • Proven ability to provide quality feedback and guidance to peers.

Additional Information:

  • Voluntary COVID-19 vaccination policy; compliance with customer or local requirements may be necessary.

  • Benefits may include company car/car allowance, health benefits (Medical, Dental, Vision), company match 401k, Employee Stock Purchase Plan, commission/bonus eligibility, flexible PTO, and sick time.

  • Annual base salary range: $60,930 - $115,100, based on qualifications, skills, and experience.

  • Over the past five years, Syneos Health has supported 94% of all Novel FDA-Approved Drugs, 95% of EMA Authorized Products, and over 200 studies across 73,000 sites and 675,000+ trial patients.

Compliance Statement:

Tasks, duties, and responsibilities listed are not exhaustive and may be reassigned. Equivalent experience, skills, and/or education may be considered. Nothing herein creates an employment contract. Syneos Health complies with the Americans with Disabilities Act and all applicable regulations regarding equal employment opportunities.