Clinical Operations Manager 2 (COM2)

Clinical Operations Manager 2 (COM2)

The COM 2 is a regional role that provides expertise across all aspects of clinical site management and/ or study management for assigned Phase I - IV studies. The COM 2 operates in line with Good Clinical Practices (ICH-GCP), applicable regulatory and legal requirements and Bayer’s standard operating procedures.

The COM 2 may be assigned work packages in areas of study start-up, site management and study management on a regional level. Either one or a combination of these work packages may be allocated to the position holder according to expertise, skill set and capacity requirements in a flexible way. The COM 2 must acquire knowledge and adequate training for work packages assigned and become proficient in independently executing assigned responsibilities.

STUDY MANAGEMENT

• Lead and oversee all operational aspects of site management on a regional or study level from protocol feasibility to study archive.
• Serve as the representative for site management on the core study team.
• Contribute to the development of the protocol, study overview, monitoring strategy and Risk Based Quality Management with regards to monitoring and operational aspects.
• Responsible and accountable for developing the monitoring plan and the study-specific training plan.
• Key contributor in the development of recruitment and retention strategies and tools.
• Act as key study contact for assigned countries. Responsible for overall deliverables regarding timelines, budget, and quality in assigned countries.
• Ensure participating country commitment aligns with study commitments.
• Provide the information required to effectively monitor and manage study activities, ensuring all relevant IT systems are updated with precise and current data.
• Oversee monitoring activities and ensure sponsor oversight through monitoring report review and co-monitoring visits.

SITE MANAGEMENT

• Act as primary contact for investigational sites.
• Verify site qualification, ensure the Investigator, and site staff meet all aspects of study delivery and commitments from site selection through close out.
• Train the Investigator and site staff on study protocol, relevant systems and operational aspects of study conduct.
• Monitor trial conduct in compliance with the study protocol, ICH-GCP and applicable regulatory requirements on time and quality. Ensure completeness of the Investigator Site File.
• Prepare and conduct onsite and/or remote monitoring activities according to monitoring plan, including complete reporting and follow up.

CLINICAL CUSTOMER ENGAGEMENT

• Cultivate and sustain customer relations with clinical trial sites, ensure effective communication, drive fit for purpose processes and work towards enhancing overall site satisfaction and engagement.
• Establish and develop strong professional relationships with clinical investigators to expand/ maintain clinical research partnership opportunities.
• Cross functional collaboration to ensure alignment of priorities and deliver the portfolio.
• Influence and challenge internal and external factors to improve clinical research delivery.

STUDY START-UP

• Lead study start-up activities in collaboration with local team.
• Provide input on site activation strategy.
• Collect and perform quality review of essential documents on country level such as IRB/IEC approvals, financial disclosure, CVs/medical licenses, etc.
• Compile and submit submission dossier (country dependent).
• Obtain any required approvals for relevant site documents (e.g., informed consent, financial disclosures).
• Prepare and distribute site start up documentation including Investigator Site File.
• Ensure timely filing of study documents at country and site level in Trial Master File (TMF).
• Ensure awareness of related local regulations and support maintenance of country intelligence.
• Provide study status monitoring and systems support (e.g. act as technical expert)
• Coordinate site and vendor payments.

QUALITY

• Proactively identify and communicate issues, taking appropriate action to prevent the recurrence of identified deviations. Ensure timely and comprehensive resolution of issues that may affectcompliance or the quality of study related activities or data.
• Maintain corrective action and preventative action plans (CAPAs) at country level.
• Contribute to the preparation, conduct, and follow-up of Site Audits and Regulatory Inspections to ensure a successful outcome.
• Oversee completeness of country/site level eTMF and conduct QC for accuracy, completeness, and adherence to ICH/GCP and Bayer QSDs.

SKILLS & QUALIFICATIONS:

Healthcare related Bachelor’s Degree or equivalent with minimum 4 years of monitoring and site management experience. Or have a combination of education and minimum 8 years of monitoring and site management experience. Experience in Spain. Languages: Effective written and verbal English and Spanish communication skills. Fundamental project management skills, Decision making, Issue resolution

Home based in Spain

Location: Spain

Application Period:

15 días

Reference Code:

891581

Division:

Pharmaceuticals

Location:

Spain : Cataluña : Barcelona

Functional Area:

Clinical Development & Operations

Position Grade:

VS 1.2

Employment Type:

Regular

Work Time:

Regular

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Av. Baix Llobregat, 3, 08970 Sant Joan Despí,

Barcelona, Espanya

+34 93 495 69 99

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