Provide Study Start-Up Specialist activities in support of assigned projects including IRB/IEC submissions,
informed consent review, essential document collection and review in preparation of site initiation and
activation. Provide leadership to junior department and project team members.

DUTIES AND RESPONSIBILITIES:

• Work closely with project teams to ensure efficient start-up processes for assigned projects in
accordance with ICH-GCP, relevant Standard Operating Procedures (SOPs) and/or Sponsor specific requirements.
• May act as Study Start-Up Specialist Lead at project level; may directly interact with customers and
sponsors as required. May serve as main point of contact for all project-specific Study Start-Up
Specialist activities.
• Forecast site-specific submission/approval timelines based on site specific information and in
accordance with Sponsor expectations and ensure they are met; if forecasted timelines are not
reached, provide clear rationale for delays and contingency plans to mitigate impact. Anticipate and
identify site issues during start-up process and resolve minor to moderate issues independently.
Communicate regularly with study team members and escalate complex issues as soon as
identified.
• Draft and/or review essential documents and templates for mass distribution to sites, distribute with
initial welcome packets and arrange for receipt of essential documents; assist with dissemination
of patient recruitment and other study materials and updates to essential documents.
• Collect, review for completeness and compliance, and track essential documents for Study Start-Up Specialist to facilitate efficient site initiation and activation. Investigate incomplete, inaccurate
or missing documents to ensure accuracy and completeness of information. Prepare study team
reports or updates regarding status of essential document collection, review and approval.
• Actively correspond with selected sites for updates regarding essential document completion,
Informed Consent Form (ICF) development and Institutional Review Board (IRB)/Independent
Ethics Committee (IEC) submissions/approvals.
• Participate in ICF development, review, negotiation and approval processes.
• Coordinate with study teams, sponsors, clinical monitoring, clinical contracts and/or other functional
areas on the priority and processing of documents leading to investigational product release, site
activation and site initiation.
• Attend project team meetings and training sessions according to project and/or Sponsor
requirements.
• Monitor number of hours/tasks available for Study Start-Up Specialist activities per project
specifications; escalated discrepancies in a timely manner.
• May serve as main point of contact for Central IRB/IECs and prepare submissions for multicenter
trials; facilitate preparation of site submissions to Local IRB/IEC as defined by local requirements.
Facilitate and process IRB/IEC Continuing Review or Re-Approvals, Protocol Amendment and
update to Investigator Brochure.
• Arrange for and/or review translation of essential documents as required. Study Start-Up Specialist II
• Assist with feasibility and site identification activities as needed.
• Ensure all relevant essential documents are submitted to Trial Master File (TMF) in a timely manner
as defined by SOPs and study-specific requirements.
• Assist with mentoring and training of department staff and new-hires.

MINIMUM JOB REQUIREMENTS / QUALIFICATIONS:

• Bachelor’s degree (BA/BS) in a science-related field preferred or equivalent combination of
education, training and experience.
• Experience working the pharmaceutical, biotechnology or CRO industry and knowledge of clinical
trials process required.
• Experience in Study Start-Up Specialist and activation and document collection and review
required.

KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED:

• Excellent oral and written communication skills.
• Excellent interpersonal and organizational skills with strong attention to detail.
• Good customer/client relationship management and proactive problem-solving skills.
• Knowledge of the principles, methods, and procedures of clinical research.
• Good computer skills including MS Word, Excel, PowerPoint, Outlook.
• Experience with ICH/GCP documentation and process preferred.
• Ability to assess, coordinate, and organize/reorganize workload of
multiple projects in accordance with project priorities/assignments and timelines with focus on
execution.

CONDITIONS OF EMPLOYMENT:

Verification of educational requirements, employment history, professional references, and
certifications/training.

WORKING CONDITIONS AND PHYSICAL EFFORT:

• Work is normally performed in a typical interior/office work environment

MedSource is an equal opportunity employer. We celebrate diversity and are committed to
creating an inclusive environment for all employees.

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